<?xml version="1.0" encoding="UTF-8"?>
<rss version="2.0">
    <channel>
        <title>Selleck--Solutions to signal transduction research</title>
        <description>Selleck is one of the world leading suppliers of high-performance life-science products. We have over 8,000 products which consist of inhibitors, antibodies, RNAis, protein and peptides those which focus on signaling pathways such as MAPK, PI3K/Akt, and apoptosis. Furthermore, compound libraries for high-throughput screening and high-content screening are also available.</description>
        <link>http://www.selleckchem.com/</link>
        <copyright>2010 Selleck Chemicals</copyright>
        <language>en-us</language>
        <lastBuildDate>Thu, 15 Dec 2011 11:28:53 +0800</lastBuildDate>
        <pubDate>Wed, 14 Dec 2011 18:44:25 +0800</pubDate>
        <generator>FeedForAll v2.0 (2.0.3.1) unlicensed version http://www.feedforall.com</generator>
        <item>
            <title>About Us</title>
            <description>
                <![CDATA[<font color="#0080ff"><b>About Selleck</b></font><br />
<br />
<font color="#0080ff"></font><br />
<font color="#0080ff"><b>What’s in it for me?</b></font><br />
Selleck is one of the world leading suppliers of high-performance life-science products. We have over 8,000 products which consist of inhibitors, antibodies, RNAis, proteins and peptides those which focus on signaling pathways such as MAPK, PI3K/Akt, and apoptosis. Furthermore, compound libraries for high-throughput screening and high-content screening are also available.<br />
<br />
<br />
<font color="#0080ff"><b>Quality</b></font><br />
Selleck pays great attention to the purity, stability and activity of the products. Not only could Selleck provides the chemical test data, such as HNMR, LC-MS and HPLC, but also provides the reviews overall evaluations of the products from the customers who have used our products. Western Blot, MTT, RT-PCR, ICH photos or figures provide a double guarantee for the biological activities of our products in life-science research. If our products have any quality problems, we will unconditionally return or replace your goods.<br />
<br />
<br />
<font color="#0280ff"><b>Support</b></font><br />
Selleck has been leading the way in biology, medical and pharmaceutical science researches, and its reagents and services have been helping scientists worldwide to make successful discoveries. Our team is dedicated to customer satisfaction and our technical experts provide professional support to ensure the best results.<br />
<br />
<br />
<font color="#0080ff"><b>Worldwide Relation</b></font><br />
Selleck has established long-term and stable relationships with more than 10,000 customers from pharmaceutical and biotech companies, universities and research institutions. Selleck has headquarters in both United States and Europe, and also has 38 distributors worldwide. We provide overnight delivery in North America and Europe.<br />
<br />
<font color="#0080ff"><b>Our goalis</b></font> to provide scientists world-wide an easy access to the most innovative life science reagents, and to help them make more significant discoveries.]]>
            </description>
            <link>http://www.selleckchem.com/aboutus.html</link>
            <guid isPermaLink="false">A3A12205-5E85-4B74-8988-E52CEDD77DEB</guid>
            <pubDate>Thu, 19 May 2011 10:21:14 +0800</pubDate>
        </item>
        <item>
            <title>Pramipexole (Mirapex) | CAS 104632-26-0 | Dopamine receptor Inhibitor | Mirapexin, Sifrol </title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Pramipexole%20%28Mirapex%29-chemical-structure-s2460.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/Pramipexole-Mirapex.html" style="color:#062074">Pramipexole (Mirapex)(Synonyms Mirapexin, Sifrol)
 </a>  (Cat No. S2460  )</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Neuro-Signaling.html" style="color:#062074">Neuro Signaling </a>  »  <a href="http://www.selleckchem.com/pathways_Dopamine-receptor.html">Dopamine receptor</a> »  <a href="http://www.selleckchem.com/products/Pramipexole-Mirapex.html"style="color:#062074">Pramipexole-Mirapex
</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Pramipexole (Mirapex) is a partial/full D2S, D2L, D3, D4 receptor agonist with a Ki of 3.9, 2.2, 0.5 and 5.1 nM for D2S, D2L, D3, D4 receptor, respectively.

			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/Pramipexole-Mirapex.html</link>
            <guid isPermaLink="false">D986DB43-60E8-4848-9EAE-824B2EB4F0CE</guid>
            <pubDate>Wed, 14 Dec 2011 18:44:25 +0800</pubDate>
        </item>
        <item>
            <title>5-hydroxymethyl tolterodine (PNU 200577) | CAS 207679-81-0 | mAChRs Inhibitor</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/5-hydroxymethyl%20tolterodine%20%28PNU%20200577%29-chemical-structure-s2659.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/5-hydroxymethyl-tolterodine-pnu-200577.html" style="color:#062074">5-hydroxymethyl tolterodine (PNU 200577)
 </a>  (Cat No. S2659  )</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_GPCR.html" style="color:#062074">GPCR </a>  »  <a href="http://www.selleckchem.com/pathways_mAChRs.html">mAChRs </a> »  <a href="http://www.selleckchem.com/products/5-hydroxymethyl-tolterodine-pnu-200577.html"style="color:#062074">5-hydroxymethyl-tolterodine-pnu-200577
</a></div>
							<strong style="color:#062074">Biological Activity:</strong>5-hydroxymethyl tolterodine (PNU 200577) is a potent muscarinic receptor antagonist with a Kb and a pA2 of 0.84 nM and 9.14, respectively.

			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/5-hydroxymethyl-tolterodine-pnu-200577.html</link>
            <guid isPermaLink="false">43B01C58-7733-4037-B3D8-26B3E277018E</guid>
            <pubDate>Wed, 14 Dec 2011 18:41:16 +0800</pubDate>
        </item>
        <item>
            <title>PH-797804 | CAS 586379-66-0 | p38 MAPK Inhibitor</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/PH-797804-chemical-structure-s2726.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/ph-797804.html" style="color:#062074">PH-797804
 </a>  (Cat No. S2726  )</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_MAPK.html" style="color:#062074">MAPK </a>  »  <a href="http://www.selleckchem.com/pathways_p38-MAPK.htmll">p38 MAPK </a> »  <a href="http://www.selleckchem.com/products/ph-797804.html"style="color:#062074">ph-797804
</a></div>
							<strong style="color:#062074">Biological Activity:</strong>PH-797804 is a highly selective, potent, and ATP-competitive p38 MAP kinase inhibitor with an IC50 of 2.3 nM.
			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/ph-797804.html</link>
            <guid isPermaLink="false">6070193B-C50D-4F2D-81AA-78B3A2D3C557</guid>
            <pubDate>Wed, 14 Dec 2011 18:37:55 +0800</pubDate>
        </item>
        <item>
            <title>Olmesartan medoxomil | CAS 144689-63-4  | RAAS Inhibitor</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Olmesartan%20medoxomil-chemical-structure-s1604.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/olmesartan-medoxomil.html" style="color:#062074">Olmesartan medoxomil
 </a>  (Cat No. S1604  )</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Hormone.html" style="color:#062074">Hormone </a>  »  <a href="http://www.selleckchem.com/pathways_RAAS.html">RAAS </a> »  <a href="http://www.selleckchem.com/products/olmesartan-medoxomil.html"style="color:#062074">olmesartan-medoxomil
</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Olmesartan medoxomil is a compound which is hydrolyzed to olmesartan that is a selective AT1 subtype angiotensin II receptor antagonist.
			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/olmesartan-medoxomil.html</link>
            <guid isPermaLink="false">00CE6AA7-FD16-4CE9-A017-48A395F6E223</guid>
            <pubDate>Wed, 14 Dec 2011 18:33:26 +0800</pubDate>
        </item>
        <item>
            <title>Crenolanib (CP-868569) | CAS 670220-88-9 | VEGFR-PDGFR Inhibitor</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Crenolanib%20%28CP-868569%29-chemical-structure-s2730.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/crenolanib-cp-868569.html" style="color:#062074">Crenolanib (CP-868569)
 </a>  (Cat No. S2730  )</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Angiogenesis_Tyrosine-Kinase.html" style="color:#062074">Angiogenesis/Tyrosine Kinase </a>  »  <a href="http://www.selleckchem.com/pathways_VEGFR-PDGFR.html">VEGFR-PDGFR </a> »  <a href="http://www.selleckchem.com/products/crenolanib-cp-868569.html"style="color:#062074">crenolanib-cp-868569
</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Crenolanib (CP-868569) is a highly selective and potent PDGFR-α inhibitor with IC50 of 0.9 and 1.8 nM against PDGFRα and PDGFRβ, respectively.
			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/crenolanib-cp-868569.html</link>
            <guid isPermaLink="false">7A0CB944-611A-489C-8CBA-037DEE02957B</guid>
            <pubDate>Wed, 14 Dec 2011 18:29:37 +0800</pubDate>
        </item>
        <item>
            <title>MK-4827 | CAS 1038915-60-4  | PARP Inhibitor</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/MK-4827-chemical-structure-s2741.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/mk-4827.html" style="color:#062074">MK-4827
 </a>  (Cat No. S2741  )</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_PARP.html" style="color:#062074">PARP </a>  »  <a href="http://www.selleckchem.com/pathways_PARP.html"style="color:#062074">PARP </a> »  <a href="http://www.selleckchem.com/products/mk-4827.html"style="color:#062074">mk-4827
</a></div>
							<strong style="color:#062074">Biological Activity:</strong>MK-4827 is a potent, selective PARP 1/2 inhibitor with IC50 of 3.8 and 2.1 nM for PARP1 and 2, respectively.

			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/mk-4827.html</link>
            <guid isPermaLink="false">C2CAA6B0-A2F4-44A3-B25B-E519B56BD675</guid>
            <pubDate>Wed, 14 Dec 2011 18:24:00 +0800</pubDate>
        </item>
        <item>
            <title>ARRY-520 | CAS 885060-09-3 | Ksp Inhibitor</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/ARRY-520-chemical-structure-s2737.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/arry-520.html" style="color:#062074">ARRY-520
 </a>  (Cat No. S2737  )</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Aurora_Ksp.html" style="color:#062074">Aurora/Ksp </a>  »  <a href="http://www.selleckchem.com/pathways_Ksp.html"style="color:#062074">Ksp </a> »  <a href="http://www.selleckchem.com/products/arry-520.html"style="color:#062074">arry-520
</a></div>
							<strong style="color:#062074">Biological Activity:</strong>ARRY-520 is a potent and selective kinesin spindle protein (KSP) inhibitor with an IC50 of 15 nM for A2780, CP70 and 01-28 cell lines in vitro.

			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/arry-520.html</link>
            <guid isPermaLink="false">6D177472-5AC5-4120-9BDC-FE8C2A2306E7</guid>
            <pubDate>Wed, 14 Dec 2011 18:17:04 +0800</pubDate>
        </item>
        <item>
            <title>SCH 900776 | CAS 891494-63-6  | Checkpoint Inhibitor</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/SCH%20900776-chemical-structure-s2735.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/sch-900776.html" style="color:#062074">SCH 900776
 </a>  (Cat No. S2735  )</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Cell-Cycle_Checkpoint.html" style="color:#062074">Cell Cycle/Checkpoint  </a>  »  <a href="http://www.selleckchem.com/pathways_Checkpoint.html"style="color:#062074">Checkpoint</a> »  <a href="http://www.selleckchem.com/products/sch-900776.html"style="color:#062074">sch-900776
</a></div>
							<strong style="color:#062074">Biological Activity:</strong>SCH 900776 is a potent and functionally selective targeting cell cycle checkpoint kinase 1 (CHK1) inhibitor with IC50 of 3 nM, 0.16 and 1.5 μM, respectively.

			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/sch-900776.html</link>
            <guid isPermaLink="false">4D36C93B-4C4F-49DD-A607-E0DF83A0C49B</guid>
            <pubDate>Wed, 14 Dec 2011 18:07:08 +0800</pubDate>
        </item>
        <item>
            <title>AV-412 | CAS 451493-31-5 | EGFR(HER) Inhibitor | MP-412</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/AV-412-chemical-structure-s2733.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/av-412.html" style="color:#062074">AV-412
 (Synonyms MP-412)
 </a>  (Cat No. S2733  )</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Angiogenesis_Tyrosine-Kinase.html" style="color:#062074">Angiogenesis/Tyrosine Kinase  </a>  »  <a href="http://www.selleckchem.com/pathways_EGFR%28HER%29.html"style="color:#062074">EGFR(HER) </a> »  <a href="http://www.selleckchem.com/products/av-412.html"style="color:#062074">av-412
</a></div>
							<strong style="color:#062074">Biological Activity:</strong>AV-412 is a second-generation, orally bioavailable dual EGFR/HER2 tyrosine kinase inhibitor.
			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/av-412.html</link>
            <guid isPermaLink="false">F26D5B38-8A4A-4F03-9992-7A35E442F56C</guid>
            <pubDate>Wed, 14 Dec 2011 17:56:01 +0800</pubDate>
        </item>
        <item>
            <title>Triciribine phosphate (NSC-280594) | CAS 61966-08-3 | Akt Inhibitor | VQD-002,TCN-P</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Triciribine%20phosphate-NSC-280594--chemical-structure-s2732.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/triciribine-phosphate-nsc-280594.html" style="color:#062074">Triciribine phosphate (NSC-280594) (Synonyms VQD-002,TCN-P) 
 </a>  (Cat No. S2732  )</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_PI3K_Akt_mTOR.html" style="color:#062074">PI3K/Akt/mTOR </a>  »  <a href="http://www.selleckchem.com/pathways_Akt.html"style="color:#062074">Akt </a> »  <a href="http://www.selleckchem.com/products/triciribine-phosphate-nsc-280594.html"style="color:#062074">Triciribine phosphate (NSC-280594)(Synonyms VQD-002,TCN-P) 
</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Triciribine phosphate (NSC-280594) is a novel potent, small-molecule Akt inhibitor.
			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/triciribine-phosphate-nsc-280594.html</link>
            <guid isPermaLink="false">60502EAA-4D2C-46B1-AA02-AB3FC312647A</guid>
            <pubDate>Wed, 14 Dec 2011 17:49:34 +0800</pubDate>
        </item>
        <item>
            <title>S3I-M2001 | CAS 1003580-86-6 | Stat Inhibitor</title>
            <description>
                <![CDATA[<table width="100%" border=0 cellpadding=1 bordercolorlight="#f0f0f0" bordercolordark="#a0a0a0" cellspacing=2>
<tr valign=top>
<td width=367 valign=middle><img alt="alt="src=" ="ttp://www.selleckchem.com/pic/digi/S3I-M2001-chemical-structure-s2734.gif""" style="margin-right:20px" ="" src="http://www.selleckchem.com/pic/digi/S3I-M2001-chemical-structure-s2734.gif" " src="http://www.selleckchem.com/pic/digi/S3I-M2001-chemical-structure-s2734.gif"><br />
</td>
<td valign=middle><b>Product:</b><a href="http://www.selleckchem.com/products/s3I-m2001.html" style="color:#062074" > S3I-M2001</a> (Cat No. S2734 )<br />
<b>Category:</b><a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074" > By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Jak_Stat.html" style="color:#062074" >Jak/Stat</a> » <a href="http://www.selleckchem.com/pathways_JAK.html" style="color:#062074" >JAK</a> » <a href="http://www.selleckchem.com/products/s3I-m2001.html" style="color:#062074" >S3I-M2001 </a><br />
<b>Biological Activity:</b>S3I-M2001 is a novel small-molecule Stat3 inhibitor with IC50 of 79, 92 and 159 µM for Stat3:Stat3, Stat1:Stat3 and Stat1:Stat1, respectively. <br />
</td>
</tr>
</table>
]]>
            </description>
            <link>http://www.selleckchem.com/products/s3I-m2001.html</link>
            <guid isPermaLink="false">67CE72A9-B87C-4A8C-8A35-59C6C42B11F7</guid>
            <pubDate>Wed, 14 Dec 2011 17:44:15 +0800</pubDate>
        </item>
        <item>
            <title>TG-101348 | CAS 936091-26-8 | JAK Inhibitor</title>
            <description>
                <![CDATA[<table width="100%" border=0 cellpadding=1 bordercolorlight="#f0f0f0" bordercolordark="#a0a0a0" cellspacing=2>
<tr valign=top>
<td width=367 valign=middle><img alt="src="http://www.selleckchem.com/pic/digi/TG-101348-chemical-structure-s2736.gif" style="margin-right:20px" " src="http://www.selleckchem.com/pic/digi/TG-101348-chemical-structure-s2736.gif"><br />
</td>
<td valign=middle><b>Product:</b><a href="http://www.selleckchem.com/products/tg-101348.html" style="color:#062074" > TG-101348</a> (Cat No. S2736 )<br />
<b>Category:</b><a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074" > By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Jak_Stat.html" style="color:#062074" >Jak/Stat</a> » <a href="http://www.selleckchem.com/pathways_JAK.html" style="color:#062074" >JAK</a> » <a href="http://www.selleckchem.com/products/tg-101348.html" style="color:#062074" >tg-101348 </a><br />
<b>Biological Activity:</b>TG-101348 is a potent, highly selective and ATP- competitive JAK2 inhibitor with an IC50 of 3 nM for JAK2 and JAK2 V617F. <br />
</td>
</tr>
</table>
]]>
            </description>
            <link>http://www.selleckchem.com/products/tg-101348.html</link>
            <guid isPermaLink="false">DD29E67C-3758-4D1A-88FD-1BF2AF9A1252</guid>
            <pubDate>Wed, 14 Dec 2011 17:32:51 +0800</pubDate>
        </item>
        <item>
            <title>PKI-402 | CAS 1173204-81-3 | PI3K Inhibitor</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/PKI-402-chemical-structure-s2739.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/pki-402.html" style="color:#062074">PKI-402
 </a>  (Cat No. S2739  )</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_PI3K_Akt_mTOR.html" style="color:#062074">PI3K/Akt/mTOR</a>  »  <a href="http://www.selleckchem.com/pathways_PI3K.html"style="color:#062074">PI3K</a> »  <a href="http://www.selleckchem.com/products/pki-402.html"style="color:#062074">PKI-402
</a></div>
							<strong style="color:#062074">Biological Activity:</strong>PKI-402 is a selective, reversible, ATP-competitive, equipotent class I phosphatidylinositol 3-kinases (PI3K) inhibitor with IC50 of 1, 7, 16 and 14 nM for PI3Kα, PI3Kβ, PI3Kγ and PI3Kδ, respectively.

			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/pki-402.html</link>
            <guid isPermaLink="false">C8A72D0C-C618-455C-944E-D1CC8B010E57</guid>
            <pubDate>Fri, 9 Dec 2011 16:54:03 +0800</pubDate>
        </item>
        <item>
            <title>GSK1070916 | CAS 942918-07-2 | Aurora Inhibitor</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/GSK1070916-chemical-structure-s2740.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/gsk1070916.html" style="color:#062074">GSK1070916
 </a>  (Cat No. S2740  )</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Aurora_Ksp.html" style="color:#062074">Aurora/Ksp</a>  »  <a href="http://www.selleckchem.com/pathways_Aurora.html"style="color:#062074">Aurora</a> »  <a href="http://www.selleckchem.com/products/gsk1070916.html"style="color:#062074">GSK1070916
 
</a></div>
							<strong style="color:#062074">Biological Activity:</strong>GSK1070916 is a novel, highly potent and selective Aurora B/C kinases ATP competitive inhibitor with an EC50 of <10 nM.

			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/gsk1070916.html</link>
            <guid isPermaLink="false">261DC57F-B335-4749-AD4D-90E9FB311BEB</guid>
            <pubDate>Fri, 9 Dec 2011 16:51:35 +0800</pubDate>
        </item>
        <item>
            <title>JTC-801 | CAS 244218-51-7  | Opioid receptor Inhibitor</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/JTC-801-chemical-structure-s2722.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/jtc-801.html" style="color:#062074">JTC-801
 </a>  (Cat No. S2722  )</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_GPCR.html" style="color:#062074">GPCR</a>  »  <a href="http://www.selleckchem.com/pathways_Opioid-receptor.html"style="color:#062074">Opioid receptor</a> »  <a href="http://www.selleckchem.com/products/jtc-801.html"style="color:#062074">JTC-801
 
</a></div>
							<strong style="color:#062074">Biological Activity:</strong>JTC-801 is a novel high affinity, selective opioid receptor- like1(ORL1) receptor antagonist with a Ki of 8.2 nM.


			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/jtc-801.html</link>
            <guid isPermaLink="false">524EE724-D01B-4B17-B77C-97B290F78107</guid>
            <pubDate>Fri, 9 Dec 2011 16:47:05 +0800</pubDate>
        </item>
        <item>
            <title>PF299804 | CAS 1110813-31-4 | EGFR(HER) Inhibitor</title>
            <description>
                <![CDATA[<table width="100%" border=0 cellpadding=1 bordercolorlight="#f0f0f0" bordercolordark="#a0a0a0" cellspacing=2>
<tr valign=top>
<td width=367 valign=middle><img alt="src="http://www.selleckchem.com/pic/digi/PF299804-chemical-structure-s2727.gif" style="margin-right:20px" " src="http://www.selleckchem.com/pic/digi/PF299804-chemical-structure-s2727.gif"><br />
</td>
<td valign=middle><b>Product:</b><a href="http://www.selleckchem.com/products/pf299804.html" style="color:#062074" > PF299804</a> (Cat No. S2727 )<br />
<b>Category:</b><a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074" > By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Angiogenesis_Tyrosine-Kinase.html" style="color:#062074" >Angiogenesis/Tyrosine Kinase</a> » <a href="http://www.selleckchem.com/pathways_EGFR%28HER%29.html" style="color:#062074" >EGFR(HER)</a> » <a href="http://www.selleckchem.com/products/pf299804.html" style="color:#062074" >PF299804 </a><br />
<b>Biological Activity:</b>PF299804 is a potent, orally available, irreversible tyrosine kinase HER 1 (EGFR), HER2 and HER4 inhibitor with IC50 of 6, 45.7 and 73.7 nM for EGFR, ERBB2 and ERBB4, respectively. <br />
</td>
</tr>
</table>
]]>
            </description>
            <link>http://www.selleckchem.com/products/pf299804.html</link>
            <guid isPermaLink="false">33E82B0B-1722-4828-B6EB-3C9FF3D06BDB</guid>
            <pubDate>Fri, 9 Dec 2011 16:43:11 +0800</pubDate>
        </item>
        <item>
            <title>SB 415286 | CAS 264218-23-7 | GSK-3 Inhibitor</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/SB%20415286-chemical-structure-s2729.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/sb-415286.html" style="color:#062074">SB 415286</a>  (Cat No. S2729  )</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_PI3K_Akt_mTOR.html" style="color:#062074">PI3K/Akt/mTOR</a>  »  <a href="http://www.selleckchem.com/pathways_GSK-3.html"style="color:#062074">GSK-3</a> »  <a href="http://www.selleckchem.com/products/sb-415286.html"style="color:#062074">SB 415286
</a></div>
							<strong style="color:#062074">Biological Activity:</strong>SB 415286 is a potent and selective cell-permeable, ATP-competitive GSK3α inhibitor with an IC50 and a Ki of 78 and 31 nM, respectively.

			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/sb-415286.html</link>
            <guid isPermaLink="false">F4F5B323-585F-46D6-BE48-C653C68BECCF</guid>
            <pubDate>Fri, 9 Dec 2011 16:33:35 +0800</pubDate>
        </item>
        <item>
            <title>CH5132799 | CAS 1007207-67-1 | PI3K Inhibitor</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/CH5132799-chemical-structure-s2699.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/ch5132799.html" style="color:#062074">CH5132799
 </a>  (Cat No. S2699  )</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_PI3K_Akt_mTOR.html" style="color:#062074">PI3K/Akt/mTOR</a>  »  <a href="http://www.selleckchem.com/pathways_PI3K.html"style="color:#062074">PI3K</a> »  <a href="http://www.selleckchem.com/products/ch5132799.html"style="color:#062074">CH5132799
</a></div>
							<strong style="color:#062074">Biological Activity:</strong>CH5132799 is a novel and selective class I PI3K inhibitor with IC50 of 0.014, 0.12, 0.5, 0.036, 5.3 and 1.6 μM for PI3Kα, PI3Kβ, PI3Kδ, PI3Kγ, PI3K C2β and mTOR, respectively.
			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/ch5132799.html</link>
            <guid isPermaLink="false">BD743774-B6C8-4FCE-B6D6-EA3AF077EE31</guid>
            <pubDate>Fri, 9 Dec 2011 16:28:34 +0800</pubDate>
        </item>
        <item>
            <title>AZ 3146 | CAS 1124329-14-1 | Ksp Inhibitor</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/AZ%203146-chemical-structure-s2731.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/az-3146.html" style="color:#062074"> AZ 3146
 </a>  (Cat No. S2731  )</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Aurora_Ksp.html" style="color:#062074">Aurora/Ksp</a>  »  <a href="http://www.selleckchem.com/pathways_Ksp.html"style="color:#062074">Ksp</a> »  <a href="http://www.selleckchem.com/products/az-3146.html"style="color:#062074">AZ 3146
</a></div>
							<strong style="color:#062074">Biological Activity:</strong>AZ 3146 is a potent and selective monopolar spindle 1 (Mps1) kinase inhibitor with an IC50 of 35 nM. 
			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/az-3146.html</link>
            <guid isPermaLink="false">DAE66937-5253-48FD-BDAB-7267B350BE21</guid>
            <pubDate>Fri, 9 Dec 2011 16:21:50 +0800</pubDate>
        </item>
        <item>
            <title>PF-03814735 | CAS 942487-16-3 | Aurora Inhibitor</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/PF-03814735-chemical-structure-s2725.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/pf-03814735.html" style="color:#062074"> PF-03814735</a>  (Cat No. S2725  )</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Aurora_Ksp.html" style="color:#062074">Aurora/Ksp</a>  »  <a href="http://www.selleckchem.com/pathways_Aurora.html"style="color:#062074">Aurora</a> »  <a href="http://www.selleckchem.com/products/pf-03814735.html"style="color:#062074">PF-03814735
</a></div>
							<strong style="color:#062074">Biological Activity:</strong>PF-03814735 is a novel, potent, orally bioavailable, reversible small-molecule Aurora kinase inhibitor with IC50 of 0.8, 5, 10 and 22 nM for Aurora 1, Aurora 2, Flt 1 and FAk, respectively.
			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/pf-03814735.html</link>
            <guid isPermaLink="false">7BA03575-4249-43F0-9EA7-95CDA8E4DECA</guid>
            <pubDate>Fri, 9 Dec 2011 16:14:55 +0800</pubDate>
        </item>
        <item>
            <title>Nepicastat hydrochloride | CAS 170151-24-3  | Dopamine receptor Inhibitor | SYN117</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Nepicastat%20hydrochloride-chemical-structure-s2695.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/nepicastat-hydrochloride.html" style="color:#062074"> Nepicastat hydrochloride</a>  (Cat No. S2695  )</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_GPCR.html" style="color:#062074">GPCR</a>  »  <a href="http://www.selleckchem.com/pathways_Dopamine-receptor.html"style="color:#062074">Dopamine receptor</a> »  <a href="http://www.selleckchem.com/products/nepicastat-hydrochloride.html"style="color:#062074">Nepicastat hydrochloride
</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Nepicastat hydrochloride is a hydrochloric acid salt form of nepicastat which is a novel, selective, and potent dopamine β-hydroxylase inhibitor with an IC50 of 8.5 and 9.0 nM for bovine and human, respectively.
			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/nepicastat-hydrochloride.html</link>
            <guid isPermaLink="false">A118D6BC-5901-4641-84B4-15A33FE6AA7F</guid>
            <pubDate>Fri, 9 Dec 2011 15:54:31 +0800</pubDate>
        </item>
        <item>
            <title>GDC-0980 (RG7422) | CAS 1032754-93-0 | mTOR Inhibitor, PI3K Inhibitor</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/GDC-0980%20%28RG7422%29-chemical-structure-s2696.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/GDC-0980-RG7422.html" style="color:#062074"> GDC-0980-RG7422</a>  (Cat No. S2696  )</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_PI3K_Akt_mTOR.html" style="color:#062074">PI3K/Akt/mTOR</a>  »  <a href="http://www.selleckchem.com/pathways_mTOR.html"style="color:#062074">mTOR / PI3K</a> »  <a href="http://www.selleckchem.com/products/GDC-0980-RG7422.html"style="color:#062074">GDC-0980-RG7422
</a></div>
							<strong style="color:#062074">Biological Activity:</strong>GDC-0980 (RG7422) is a selective, dual PI3 Kinase and mTOR Kinase inhibitor with IC50 of 5, 27, 7, and 14 nM for PI3Kα, β, δ, and γ, respectively.
			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/GDC-0980-RG7422.html</link>
            <guid isPermaLink="false">8A873A50-CD80-4CDE-BB1D-5969964322D0</guid>
            <pubDate>Thu, 8 Dec 2011 16:02:39 +0800</pubDate>
        </item>
        <item>
            <title>GSK1838705A | CAS 1116235-97-2 | IGF-1R Inhibitor</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/GSK1838705A-chemical-structure-s2703.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/gsk1838705a.html" style="color:#062074">GSK1838705A</a>  (Cat No. S2703)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Angiogenesis_Tyrosine-Kinase.html" style="color:#062074">Angiogenesis/Tyrosine Kinase</a> » <a href="http://www.selleckchem.com/pathways_IGF-1R.html" style="color:#062074">IGF-1R</a> » <a href="http://www.selleckchem.com/products/gsk1838705a.html"style="color:#062074">gsk1838705a</a></div>
							<strong style="color:#062074">Biological Activity:</strong>GSK1838705A is a potent small-molecule IGF-IR, the insulin receptor and anaplastic lymphoma kinase (ALK) inhibitor with IC50 of 2.0, 1.6 and 0.5 nM, respectively.
			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/gsk1838705a.html</link>
            <guid isPermaLink="false">41255D72-223E-4A9A-8803-B4670F9D9C79</guid>
            <pubDate>Fri, 11 Nov 2011 11:57:21 +0800</pubDate>
        </item>
        <item>
            <title>Arecoline | CAS 300-08-3  | AChR Inhibitor</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Arecoline-chemical-structure-s2614.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/arecoline.html" style="color:#062074">Arecoline</a>  (Cat No. S2614)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Neuro-Signaling.html" style="color:#062074">Neuro Signaling</a> » <a href="http://www.selleckchem.com/pathways_AChR.html" style="color:#062074">AChR</a> » <a href="http://www.selleckchem.com/products/arecoline.html"style="color:#062074">arecoline</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Arecoline is a muscarinic acetylcholine receptor agonist. 
			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/arecoline.html</link>
            <guid isPermaLink="false">788BF53B-5F8D-457F-BF5C-263BF3CBDB2C</guid>
            <pubDate>Fri, 11 Nov 2011 11:53:03 +0800</pubDate>
        </item>
        <item>
            <title>AC220 (Quizartinib) | CAS 950769-58-1 | FLT-3 Inhibitor</title>
            <description>
                <![CDATA[<table width="100%" border=0 cellpadding=1 bordercolorlight="#f0f0f0" bordercolordark="#a0a0a0" cellspacing=2>
<tr valign=top>
<td width=367 valign=middle><img alt="src="http://www.selleckchem.com/pic/digi/AC220.gif" style="margin-right:20px" " src="http://www.selleckchem.com/pic/digi/AC220.gif"><br />
</td>
<td valign=middle><b>Product:</b><a href="http://www.selleckchem.com/search.jsp?searchtxt=S1526" style="color:#062074"> AC220 (Quizartinib)</a> (Cat No. S1526)<br />
<b>Category:</b><a href="http://www.selleckchem.com/pharmacologicalact.html"> By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Angiogenesis_Tyrosine-Kinase.html" style="color:#062074">Angiogenesis/Tyrosine Kinase</a> » <a href="http://www.selleckchem.com/pathways_FLT-3.html" style="color:#062074">FLT-3</a> » <a href="http://www.selleckchem.com/search.jsp?searchtxt=S1526" style="color:#062074">AC-220</a><br />
<b>Biological Activity:</b>AC220 (Quizartinib) is a uniquely potent and selective FLT3 inhibitor with IC50 of 0.56 ± 0.3 nM and >10 mM for MC4-11 and A375, respectively. <br />
</td>
</tr>
</table>]]>
            </description>
            <link>http://www.selleckchem.com/search.jsp?searchtxt=S1526</link>
            <guid isPermaLink="false">544B79F0-AAF8-4247-A8B2-9E2FBAEA7B2E</guid>
            <pubDate>Fri, 11 Nov 2011 11:37:12 +0800</pubDate>
        </item>
        <item>
            <title>Heparin sodium 150 U/mg | CAS 9041-08-1</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Heparin%20sodium.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/Heparin-sodium.html" style="color:#062074">Heparin sodium 150 U/mg</a>  (Cat No. S1346)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/researcharea.html" style="color:#062074">By Research Area</a> » <a href="http://www.selleckchem.com/research_Cardiovascular-Disease.html" style="color:#062074">Cardiovascular Disease</a> » <a href="http://www.selleckchem.com/products/Heparin-sodium.html"style="color:#062074">Heparin sodium</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Heparin sodium 150 U/mg is a sodium salt of heparin which is a naturally-occurring anticoagulant used for anticoagulation for cardiovascular disease. 

			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/Heparin-sodium.html</link>
            <guid isPermaLink="false">5D7A0427-F226-4A28-A889-F859FEDD25B0</guid>
            <pubDate>Fri, 11 Nov 2011 11:30:56 +0800</pubDate>
        </item>
        <item>
            <title>AMG 900 | CAS 945595-80-2 | Aurora Inhibitor</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/AMG%20900-chemical-structure-s2719.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/amg-900.html" style="color:#062074">AMG 900</a>  (Cat No. S2719)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Aurora_Ksp.html" style="color:#062074">Aurora/Ksp</a> » <a href="http://www.selleckchem.com/pathways_Aurora.html" style="color:#062074">Aurora</a> » <a href="http://www.selleckchem.com/products/amg-900.html"style="color:#062074">amg 900</a></div>
							<strong style="color:#062074">Biological Activity:</strong>AMG 900 is a novel potent and highly selective Pan-aurora kinase inhibitor with an IC50 of median 3.5 nM.
			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/amg-900.html</link>
            <guid isPermaLink="false">0C7284B4-BE00-40E5-A556-1A08AB71391B</guid>
            <pubDate>Fri, 11 Nov 2011 11:28:05 +0800</pubDate>
        </item>
        <item>
            <title>ZM 336372 | CAS 208260-29-1 | B-Raf Inhibitor</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/zm-336372.html" style="color:#062074">ZM 336372</a>  (Cat No. S2720)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_MAPK.html" style="color:#062074">MAPK</a> » <a href="http://www.selleckchem.com/pathways_B-Raf.html" style="color:#062074">B-Raf</a> » <a href="http://www.selleckchem.com/products/zm-336372.html"style="color:#062074">zm 336372</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Zm 336372 is a potent, selective c-Raf inhibitor with an IC50 of 70 nM for inhibition of human c-Raf in vitro. respectively.
			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/zm-336372.html</link>
            <guid isPermaLink="false">DAEC7F36-F4F1-4F16-8BC5-747B66540DDE</guid>
            <pubDate>Fri, 11 Nov 2011 11:20:50 +0800</pubDate>
        </item>
        <item>
            <title>YO-01027 | CAS 209984-56-5 | Y-secretase Inhibitor</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/YO-01027-chemical-structure-s2711.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/yo-01027.html" style="color:#062074">YO-01027</a>  (Cat No. S2711)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Wnt_Hedgehog_Notch.html" style="color:#062074">Wnt/Hedgehog/Notch</a> » <a href="http://www.selleckchem.com/pathways_Y-secretase.html" style="color:#062074">Y-secretase</a> » <a href="http://www.selleckchem.com/products/yo-01027.html"style="color:#062074">yo-01027</a></div>
							<strong style="color:#062074">Biological Activity:</strong>YO-01027 is a dipeptidic gamma-secretase inhibitor with IC50 of 2.6 and 2.9 nM for the proteolysis of APPL and Notch, respectively.
			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/yo-01027.html</link>
            <guid isPermaLink="false">F6740748-0BAC-421C-A958-A84BDE9D48D2</guid>
            <pubDate>Fri, 11 Nov 2011 11:11:09 +0800</pubDate>
        </item>
        <item>
            <title>CP-91149 | CAS 186392-40-5</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/CP-91149-chemical-structure-s2717.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/cp-91149.html" style="color:#062074">CP-91149</a>  (Cat No. S2717)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Others.html" style="color:#062074">Others</a> » » <a href="http://www.selleckchem.com/products/cp-91149.html"style="color:#062074">cp-91149</a></div>
							<strong style="color:#062074">Biological Activity:</strong>CP-91149 is a human liver glycogen phosphorylase α (HLGPα) inhibitor with an IC50 of 0.13 μM in the presence of 7.5 mM glucose.
			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/cp-91149.html</link>
            <guid isPermaLink="false">E9CBB7C6-E942-4772-AB77-3152F28E7D63</guid>
            <pubDate>Fri, 11 Nov 2011 11:04:24 +0800</pubDate>
        </item>
        <item>
            <title>Peramivir  Trihydrate | CAS 1041434-82-5</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Peramivir%20%20Trihydrate-chemical-structure-s2716.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/peramivir--trihydrate.html#" style="color:#062074">Peramivir Trihydrate</a>  (Cat No. S2716)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/researcharea.html" style="color:#062074">By Research Area</a> » <a href="http://www.selleckchem.com/research_Neurological-Disease.html" style="color:#062074">Neurological Disease</a>  » <a href="http://www.selleckchem.com/products/peramivir--trihydrate.html#"style="color:#062074">peramivir trihydrate</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Peramivir Trihydrate is a trihydrate of the anti-infection agent peramivir (RWJ-270201,BCX-1812) which is a transition-state analogue and a potent, specific influenza viral neuraminidase inhibitor with an IC50 of median 0.09 nM.

			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/peramivir--trihydrate.html#</link>
            <guid isPermaLink="false">B878A8A3-CC4F-401E-8CAB-1FE7892A8819</guid>
            <pubDate>Fri, 11 Nov 2011 10:40:22 +0800</pubDate>
        </item>
        <item>
            <title>LY-411575 | CAS 209984-57-6</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/LY-411575-chemical-structure-s2714.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/ly-411575.html" style="color:#062074">LY-411575</a>  (Cat No. S2714)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Wnt_Hedgehog_Notch.html" style="color:#062074">Wnt/Hedgehog/Notch</a> » » <a href="http://www.selleckchem.com/products/ly-411575.html"style="color:#062074">ly-411575</a></div>
							<strong style="color:#062074">Biological Activity:</strong>LY-411575 is a selective, cell permeable, small molecule gamma secretase inhibitor with an IC50 of 0.1 nM for APP23 and APP51/16 primary neurons.

			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/ly-411575.html</link>
            <guid isPermaLink="false">F5922D7D-87B7-427A-89AA-E3F06115C89E</guid>
            <pubDate>Fri, 11 Nov 2011 10:35:51 +0800</pubDate>
        </item>
        <item>
            <title>LY-310762 | CAS 192927-92-7  | Serotonin receptor Inhibitor</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/LY-310762-chemical-structure-s2669.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/ly-310762.html" style="color:#062074">LY-310762</a>  (Cat No. S2669)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_GPCR.html" style="color:#062074">GPCR</a>  » <a href="http://www.selleckchem.com/pathways_Serotonin-receptor.html"style="color:#062074">Serotonin receptor</a> » <a href="http://www.selleckchem.com/products/ly-310762.html"style="color:#062074">ly-310762</a></div>
							<strong style="color:#062074">Biological Activity:</strong>LY-310762 is a potent and selective 5-HT1D serotonin receptor antagonist with an EC50 of 31 nM.
			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/ly-310762.html</link>
            <guid isPermaLink="false">00DBFCBF-1818-4083-8138-08D7208DA286</guid>
            <pubDate>Fri, 11 Nov 2011 10:32:43 +0800</pubDate>
        </item>
        <item>
            <title>PCI-32765 | CAS 936563-96-1</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/PCI-32765-chemical-structure-s2680.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/pci-32765.html" style="color:#062074">PCI-32765</a>  (Cat No. S2680)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Others.html" style="color:#062074">Others</a> » » <a href="http://www.selleckchem.com/products/pci-32765.html"style="color:#062074">pci-32765</a></div>
							<strong style="color:#062074">Biological Activity:</strong>PCI-32765 is a high potent irreversible BTK inhibitor with an IC50 of 0.46 nM for the purified Btk.
			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/pci-32765.html</link>
            <guid isPermaLink="false">A72752AF-9EFA-47B2-8A4A-BC8FA2E29437</guid>
            <pubDate>Fri, 11 Nov 2011 10:24:26 +0800</pubDate>
        </item>
        <item>
            <title>TAK-901 | CAS 934541-31-8 | Aurora Inhibitor</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/TAK-901-chemical-structure-s2718.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/tak-901.html" style="color:#062074">TAK-901</a>  (Cat No. S2718)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Aurora_Ksp.html" style="color:#062074">Aurora/Ksp</a>  » <a href="http://www.selleckchem.com/pathways_Aurora.html"style="color:#062074">Aurora</a> » <a href="http://www.selleckchem.com/products/tak-901.html"style="color:#062074">tak-901</a></div>
							<strong style="color:#062074">Biological Activity:</strong>TAK-901 is a small-molecule inhibitor of the serine-threonine kinase Aurora B with potential antineoplastic activity.
			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/tak-901.html</link>
            <guid isPermaLink="false">D714DA9E-4FB7-4587-A77F-3115D8F0D02B</guid>
            <pubDate>Fri, 11 Nov 2011 10:20:18 +0800</pubDate>
        </item>
        <item>
            <title>KX2-391 | CAS 897016-82-9 | Src-bcr-Abl Inhibitor</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/KX2-391-chemical-structure-s2700.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/kx2-391.html" style="color:#062074">KX2-391</a>  (Cat No. S2700)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Angiogenesis_Tyrosine-Kinase.html" style="color:#062074">Angiogenesis/Tyrosine Kinase</a>  » <a href="http://www.selleckchem.com/pathways_Src-bcr-Abl.html"style="color:#062074">Src-bcr-Abl</a> » <a href="http://www.selleckchem.com/products/kx2-391.html"style="color:#062074">kx2-391</a></div>
							<strong style="color:#062074">Biological Activity:</strong>KX2-391 is a synthetic, orally bioavailable small molecule and non-ATP competitive Src tyrosine kinase signaling inhibitor with an IC50 of average 72 nM.
			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/kx2-391.html</link>
            <guid isPermaLink="false">F98306EA-AF9C-4093-AB9F-37AD19B2FCE8</guid>
            <pubDate>Fri, 11 Nov 2011 10:15:48 +0800</pubDate>
        </item>
        <item>
            <title>WAY-362450 | CAS 629664-81-9</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/WAY-362450-chemical-structure-s2694.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/way-362450.html" style="color:#062074">WAY-362450</a>  (Cat No. S2694)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Others.html" style="color:#062074">Others
</a>  » » <a href="http://www.selleckchem.com/products/way-362450.html"style="color:#062074">way-362450</a></div>
							<strong style="color:#062074">Biological Activity:</strong>WAY-362450 is a highly potent, selective, and orally active farnesoid X receptor (FXR) agonist with an EC50 of 4 nM.
			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/way-362450.html</link>
            <guid isPermaLink="false">D743C936-2F46-41A0-8FE6-B895978FA485</guid>
            <pubDate>Fri, 11 Nov 2011 10:12:57 +0800</pubDate>
        </item>
        <item>
            <title>A-769662 | CAS 844499-71-4</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/A-769662-chemical-structure-s2697.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/a-769662.html" style="color:#062074">A-769662</a>  (Cat No. S2697)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Others.html" style="color:#062074">Others
</a>  » » <a href="http://www.selleckchem.com/products/a-769662.html"style="color:#062074">a-769662</a></div>
							<strong style="color:#062074">Biological Activity:</strong>A-769662 is a potent, reversible AMP-activated protein kinase (AMPK) activator with an EC50 of 0.8 μM.
			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/a-769662.html</link>
            <guid isPermaLink="false">CE46ACB9-43F3-4B10-A1C1-0CCBE4E12F06</guid>
            <pubDate>Fri, 11 Nov 2011 10:05:45 +0800</pubDate>
        </item>
        <item>
            <title>TG101209 | CAS 936091-14-4 | FLT-3 Inhibitor, JAK Inhibitor</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/TG101209-chemical-structure-s2692.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/tg101209.html" style="color:#062074"> TG101209</a>  (Cat No. S2692)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Jak_Stat.html" style="color:#062074">Jak/Stat</a>  »<a href="http://www.selleckchem.com/pathways_FLT-3.html">FLT-3</a>/<a href="http://www.selleckchem.com/pathways_JAK.html" style="color:#062074">JAK</a>  »  <a href="http://www.selleckchem.com/products/tg101209.html"style="color:#062074">tg101209</a></div>
							<strong style="color:#062074">Biological Activity:</strong>TG101209 is a potent and small molecule JAK2-selective kinase inhibitor with IC50 of 6, 25, 17 and 169 nM for JAK2, FLT3, RET and JAK3, respectively.
			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/tg101209.html</link>
            <guid isPermaLink="false">2A11A323-DEC2-4081-B502-9649CDECAB71</guid>
            <pubDate>Fri, 11 Nov 2011 09:53:35 +0800</pubDate>
        </item>
        <item>
            <title>BRL-15572 | CAS 193611-72-2  | Serotonin receptor Inhibitor</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/BRL-15572-chemical-structure-s2677.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/brl-15572.html" style="color:#062074">brl-15572 </a>  (Cat No. S2677 )</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Neuro-Signaling.html" style="color:#062074">Neuro Signaling</a>  »  <a href="http://www.selleckchem.com/pathways_Serotonin-receptor.html"style="color:#062074">Serotonin receptor</a> »  <a href="http://www.selleckchem.com/products/brl-15572.html"style="color:#062074">brl-15572</a></div>
							<strong style="color:#062074">Biological Activity:</strong>BRL-15572 is a hydrochloride salt form of BRL-15572 which is a selective serotonin receptor subtype 5-HT1D antagonist with an IC50 of 260 μM.

			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/brl-15572.html</link>
            <guid isPermaLink="false">4F2664D1-D559-4953-A564-0FCB01584EF8</guid>
            <pubDate>Fri, 11 Nov 2011 09:38:06 +0800</pubDate>
        </item>
        <item>
            <title>NSC-207895 (XI-006) | CAS 58131-57-0 | p53 Inhibitor |</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/NSC-207895%20%28XI-006%29-chemical-structure-s2678.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/nsc-207895-%28xi-006%29.html" style="color:#062074">NSC-207895 </a>  (Cat No. S2678 )</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Apoptosis.html" style="color:#062074">Apoptosis</a>  »  <a href="http://www.selleckchem.com/pathways_p53.html"style="color:#062074">p53</a> »  <a href="http://www.selleckchem.com/products/nsc-207895-%28xi-006%29.html"style="color:#062074">nsc-207895 (xi-006)</a></div>
							<strong style="color:#062074">Biological Activity:</strong>NSC-207895 (XI-006) is a derivative of nitrobenzofuroxan and an anticancer agent with EC50.
			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/nsc-207895-%28xi-006%29.html</link>
            <guid isPermaLink="false">DC493A45-1944-44B3-8628-6749E2A7E210</guid>
            <pubDate>Fri, 11 Nov 2011 09:17:05 +0800</pubDate>
        </item>
        <item>
            <title>Ketanserin | CAS 74050-98-9 | Serotonin receptor Inhibitor | R 41468</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Ketanserin.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/Ketanserin-Vulketan-Gel.html" style="color:#062074"> Ketanserin</a>  (Cat No. S2232 )</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_GPCR.html" style="color:#062074">GPCR</a>  »  <a href="http://www.selleckchem.com/pathways_Serotonin-receptor.html"style="color:#062074">Serotonin receptor</a> »  <a href="http://www.selleckchem.com/products/Ketanserin-Vulketan-Gel.html"style="color:#062074">Ketanserin</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Ketanserin is specific 5-HT2A serotonin receptor antagonist with a Ki of 2.5 nM for rat and human 5-HT2A.
			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/Ketanserin-Vulketan-Gel.html</link>
            <guid isPermaLink="false">01B80112-125A-42FD-A1DA-38FAF3096B50</guid>
            <pubDate>Thu, 10 Nov 2011 16:36:38 +0800</pubDate>
        </item>
        <item>
            <title>PF-04929113 | CAS 908115-27-5  | SNX-5422</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/PF-04929113-chemical-structure-s2656.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/pf-04929113.html" style="color:#062074"> A-769662</a>  (Cat No. S2656)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Proteases_HSP90_HSP70.html" style="color:#062074">Proteases/HSP90/HSP70</a>  »  <a href="http://www.selleckchem.com/products/pf-04929113.html"style="color:#062074">PF-04929113</a></div>
							<strong style="color:#062074">Biological Activity:</strong>PF-04929113 is a potent and selective Hsp90 inhibitor with an IC50 of median 50 nM. 
			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/pf-04929113.html</link>
            <guid isPermaLink="false">CB234E0E-4BFF-4AD0-9F8D-12E7FF68F785</guid>
            <pubDate>Thu, 10 Nov 2011 15:06:06 +0800</pubDate>
        </item>
        <item>
            <title>Geldanamycin | CAS cas:30562-34-6 | HSP-90 Inhibitor</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Geldanamycin-chemical-structure-s2713.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/geldanamycin.html" style="color:#062074"> Geldanamycin</a>  (Cat No. S2713)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Proteases_HSP90_HSP70.html" style="color:#062074">Proteases/HSP90/HSP70</a>  »  <a href="http://www.selleckchem.com/pathways_HSP-90.html"style="color:#062074">HSP-90</a> »  <a href="http://www.selleckchem.com/products/geldanamycin.html"style="color:#062074">geldanamycin</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Geldanamycin is a benzoquinone ansamycin antibiotic that binds to Hsp90 (Heat Shock Protein 90) and alters its function.
			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/geldanamycin.html</link>
            <guid isPermaLink="false">7629ABDC-C873-411D-99EB-6E5618E766B9</guid>
            <pubDate>Thu, 10 Nov 2011 14:52:48 +0800</pubDate>
        </item>
        <item>
            <title>PF-04929113 | CAS 908115-27-5  | SNX-5422</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/PF-04929113-chemical-structure-s2656.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/pf-04929113.html" style="color:#062074"> PF-04929113</a>  (Cat No. S2656)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Others.html" style="color:#062074">Others
</a>  »  <a href="http://www.selleckchem.com/products/pf-04929113.html"style="color:#062074">pf-04929113</a></div>
							<strong style="color:#062074">Biological Activity:</strong>PF-04929113 is a potent and selective Hsp90 inhibitor with an IC50 of median 50 nM. 
			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/pf-04929113.html</link>
            <guid isPermaLink="false">48853988-BB37-467A-8B08-055F3E16968F</guid>
            <pubDate>Thu, 13 Oct 2011 16:34:48 +0800</pubDate>
        </item>
        <item>
            <title>BMY 7378 | CAS 21102-95-4</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/BMY%207378-chemical-structure-s2691.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/bmy-7378.html" style="color:#062074"> BMY 7378</a>  (Cat No. S2691)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Others.html" style="color:#062074">Others
</a>  »  <a href="http://www.selleckchem.com/products/bmy-7378.html"style="color:#062074">bmy 7378</a></div>
							<strong style="color:#062074">Biological Activity:</strong>BMY 7378 is a 5-HT1A receptor weak partial agonist/antagonist and α1D-adrenergic receptor antagonist with Ki values of 2.8 and 0.6 μM for cloned rat rat α1A and hamster α1B receptors, respectively.
			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/bmy-7378.html</link>
            <guid isPermaLink="false">116489FB-2206-4396-B2C5-A5E7F7EB1A57</guid>
            <pubDate>Thu, 13 Oct 2011 16:31:32 +0800</pubDate>
        </item>
        <item>
            <title>ADX-47273 | CAS 851881-60-2 | mGluR2/mGluR3 Inhibitor</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/ADX-47273-chemical-structure-s2690.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/adx-47273.html" style="color:#062074">ADX-47273</a>  (Cat No. S2690)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Others.html" style="color:#062074">Others
</a>  » <a href="http://www.selleckchem.com/pathways_mGluR2_mGluR3.html"style="color:#062074">mGluR2/mGluR3</a>» <a href="http://www.selleckchem.com/products/adx-47273.html"style="color:#062074">ADX-47273</a></div>
							<strong style="color:#062074">Biological Activity:</strong>ADX-47273 is a novel, potent and selective metabotropic glutamate receptor 5 allosteric modulator with an EC50 of 170 nM in human embryonic kidney 293 cells expressing rat mGlu5.
			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/adx-47273.html</link>
            <guid isPermaLink="false">4054DF75-AD34-448E-A317-31380DC28D2D</guid>
            <pubDate>Thu, 13 Oct 2011 16:28:37 +0800</pubDate>
        </item>
        <item>
            <title>ICG-001 | CAS 780757-88-2 | Wnt Inhibitor</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/ICG-001-chemical-structure-s2662.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/icg-001.html" style="color:#062074">ICG-001</a>  (Cat No. S2662)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Wnt_Hedgehog_Notch.html" style="color:#062074">Wnt/Hedgehog/Notch </a>  » <a href="http://www.selleckchem.com/pathways_MEK.html"style="color:#062074">MEK</a> » <a href="http://www.selleckchem.com/pathways_Wnt.html"style="color:#062074">WNT</a> » <a href="http://www.selleckchem.com/products/icg-001.html"style="color:#062074">icg-001</a></div>
							<strong style="color:#062074">Biological Activity:</strong>ICG-001 is a selective Wnt/β-catenin signalling inhibitor with an IC50 of 3μM.
			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/icg-001.html</link>
            <guid isPermaLink="false">74EA6D1B-6FBA-433C-97A9-E249AAFDB0B7</guid>
            <pubDate>Thu, 13 Oct 2011 16:22:57 +0800</pubDate>
        </item>
        <item>
            <title>GSK1120212 (JTP-74057) | CAS 871700-17-3 | MEK Inhibitor</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/GSK1120212-JTP-74057-chemical-structure-s2673.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/gsk1120212-(jtp-74057).html" style="color:#062074">gsk1120212 (jtp-74057)</a>  (Cat No. S2673)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_MAPK.html" style="color:#062074"> MAPK
</a>  » <a href="http://www.selleckchem.com/pathways_MEK.html"style="color:#062074">MEK</a> » <a href="http://www.selleckchem.com/products/gsk1120212-(jtp-74057).html"style="color:#062074">gsk1120212 (jtp-74057)</a></div>
							<strong style="color:#062074">Biological Activity:</strong>GSK1120212 (JTP-74057) is a reversible, selective, allosteric MEK1/MEK2 kinase activity inhibitor with IC50 of 0.7 and 0.9 nM for MEK1 and MEK2.
			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/gsk1120212-(jtp-74057).html</link>
            <guid isPermaLink="false">24F9CFC2-372E-4467-AF82-E5A699AE67E0</guid>
            <pubDate>Thu, 13 Oct 2011 16:20:03 +0800</pubDate>
        </item>
        <item>
            <title>Clinofibrate | CAS 30299-08-2 | Lipoclin</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Clinofibrate-chemical-structure-s2664.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/clinofibrate.html" style="color:#062074">clinofibrate</a>  (Cat No. S2664)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Others.html" style="color:#062074"> Others</a>  » <a href="http://www.selleckchem.com/products/clinofibrate.html"style="color:#062074">clinofibrate</a></div>
							<strong style="color:#062074">Biological Activity:</strong>http://www.selleckchem.com/products/clinofibrate.html
			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/clinofibrate.html</link>
            <guid isPermaLink="false">554D0323-1BE4-4567-803F-81304257146E</guid>
            <pubDate>Thu, 13 Oct 2011 16:15:35 +0800</pubDate>
        </item>
        <item>
            <title>Carvedilol | CAS 72956-09-3 | adrenergic receptor Inhibitor | Coreg, Dilatrend</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Carvedilol-chemical-structure-s1831.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/carvedilol.html" style="color:#062074">Carvedilol</a>  (Cat No. S1831)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_GPCR.html" style="color:#062074"> GPCR
</a>  » <a href="http://www.selleckchem.com/pathways_adrenergic-receptor.html"style="color:#062074">adrenergic receptor
</a> » <a href="http://www.selleckchem.com/products/carvedilol.html"style="color:#062074">carvedilol</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Carvedilol is a non-selective beta blocker/alpha-1 blocker with an IC50 of 3.8 μM for inhibition of LDL oxidation.
			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/carvedilol.html</link>
            <guid isPermaLink="false">DAE9EEC3-4753-4E23-BF75-7E7524A0AA06</guid>
            <pubDate>Thu, 13 Oct 2011 16:11:29 +0800</pubDate>
        </item>
        <item>
            <title>Calcium levofolinate (Calcium Folinate) | CAS 80433-71-2</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Calcium%20levofolinate-Calcium%20Folinate-chemical-structure-s2588.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/betaine.html" style="color:#062074">Calcium levofolinate (Calcium Folinate)</a>  (Cat No. S2588)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/products/gw3965.html" style="color:#062074">By Research Area</a> » <a href="http://www.selleckchem.com/research_Others.html" style="color:#062074"> Others</a>  » <a href="http://www.selleckchem.com/products/calcium-levofolinate-(calcium-folinate).html"style="color:#062074">calcium levofolinate (calcium folinate)</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Betaine is a hydrochloride of betaine that is a non-essential nutrient.
			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/calcium-levofolinate-(calcium-folinate).html</link>
            <guid isPermaLink="false">08C72F0B-5351-4148-B719-0D05A206CC7D</guid>
            <pubDate>Thu, 13 Oct 2011 16:08:45 +0800</pubDate>
        </item>
        <item>
            <title>Brompheniramine | CAS 980-71-2 | histamine Inhibitor</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Brompheniramine-chemical-structure-s1829.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/brompheniramine.html" style="color:#062074">Brompheniramine</a>  (Cat No. S1829)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Neuro-Signaling.html" style="color:#062074"> Neuro Signaling</a>  » <a href="http://www.selleckchem.com/pathways_histamine.html"style="color:#062074">histamine</a> » <a href="http://www.selleckchem.com/products/arecoline.html"style="color:#062074">arecoline</a>» <a href="http://www.selleckchem.com/products/brompheniramine.html"style="color:#062074">brompheniramine</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Brompheniramine is a maleate salt of brompheniramine that is a histamine H1 receptors antagonist.
			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/brompheniramine.html</link>
            <guid isPermaLink="false">D1472570-DAD9-4A72-B718-AC7C27A69ADF</guid>
            <pubDate>Thu, 13 Oct 2011 16:02:30 +0800</pubDate>
        </item>
        <item>
            <title>Betaine | CAS 590-46-5</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Betaine-chemical-structure-s2580.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/betaine.html" style="color:#062074">betaine</a>  (Cat No. S2416)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/products/gw3965.html" style="color:#062074">By Research Area</a> » <a href="http://www.selleckchem.com/research_Metabolic-Disease.html" style="color:#062074"> Metabolic Disease</a>  » <a href="http://www.selleckchem.com/products/betaine.html"style="color:#062074">betaine</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Betaine is a hydrochloride of betaine that is a non-essential nutrient.
			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/betaine.html</link>
            <guid isPermaLink="false">48A71FD7-FE86-407A-B96A-E4B2D16634E0</guid>
            <pubDate>Thu, 13 Oct 2011 15:58:35 +0800</pubDate>
        </item>
        <item>
            <title>Arecoline | CAS 300-08-3  | AChR Inhibitor</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Arecoline-chemical-structure-s1825.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/arecoline.html" style="color:#062074">Arecoline
</a>  (Cat No. S1825)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Neuro-Signaling.html" style="color:#062074"> Neuro Signaling</a>  » <a href="http://www.selleckchem.com/pathways_AChR.html"style="color:#062074">AChR
</a> » <a href="http://www.selleckchem.com/products/arecoline.html"style="color:#062074">arecoline</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Arecoline is a muscarinic acetylcholine receptor agonist.
			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/arecoline.html</link>
            <guid isPermaLink="false">77ACCC7B-98A7-4EE6-9BC0-14FDAB5B7729</guid>
            <pubDate>Thu, 13 Oct 2011 15:51:59 +0800</pubDate>
        </item>
        <item>
            <title>Amilorida | CAS 17440-83-4 | MK-870</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Amilorida-chemical-structure-s2560.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/amilorida.html" style="color:#062074">Amilorida</a>  (Cat No. S2560)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Ion-channel.html" style="color:#062074"> Ion channel</a>  » <a href="http://www.selleckchem.com/products/amilorida.html"style="color:#062074">Amilorida</a> </div>
							<strong style="color:#062074">Biological Activity:</strong>Amilorida is a potent epithelial sodium channel blocker.
			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/amilorida.html</link>
            <guid isPermaLink="false">2CC9660F-5996-4B1E-B79C-0E23CE69B162</guid>
            <pubDate>Mon, 10 Oct 2011 16:05:52 +0800</pubDate>
        </item>
        <item>
            <title>Ribitol (Adonitol) | CAS 488-81-3  | Adonite</title>
            <description>
                <![CDATA[<table width="100%" border=0 cellpadding=1 bordercolorlight="#f0f0f0" bordercolordark="#a0a0a0" cellspacing=2>
<tr valign=top>
<td width=367 valign=middle><img alt="src="http://www.selleckchem.com/pic/digi/Ribitol-Adonitol-chemical-structure-s2612.gif" style="margin-right:20px" " src="http://www.selleckchem.com/pic/digi/Ribitol-Adonitol-chemical-structure-s2612.gif"><br />
</td>
<td valign=middle><b>Product:</b><a href="http://www.selleckchem.com/products/ribitol-(adonitol).html" style="color:#062074"> Ribitol (Adonitol)</a> (Cat No. S2612)<br />
<b>Category:</b><a href="http://www.selleckchem.com/products/gw3965.html" style="color:#062074"> By Research Area</a> » <a href="http://www.selleckchem.com/research_Metabolic-Disease.html" style="color:#062074">Metabolic Disease </a>» <a href="http://www.selleckchem.com/products/ribitol-(adonitol).html" style="color:#062074">Ribitol (Adonitol)</a><br />
<b>Biological Activity:</b>Ribitol (Adonitol) is a sugar alcohol formed by the reduction of ribose. <br />
</td>
</tr>
</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/ribitol-(adonitol).html</link>
            <guid isPermaLink="false">04375A26-A5D4-49BE-A216-E75D5886D4BC</guid>
            <pubDate>Mon, 10 Oct 2011 16:01:29 +0800</pubDate>
        </item>
        <item>
            <title>Chondroitin sulfate | CAS 9007-28-7</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Chondroitin%20sulfate-chemical-structure-s2416.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/chondroitin-sulfate.html" style="color:#062074">Chondroitin sulfate</a>  (Cat No. S2416)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/products/gw3965.html" style="color:#062074">By Research Area</a> » <a href="http://www.selleckchem.com/research_Immunology.html" style="color:#062074"> Immunology </a>  » <a href="http://www.selleckchem.com/products/chondroitin-sulfate.html"style="color:#062074">Chondroitin sulfate</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Chondroitin sulfate is a kind of sulfated glycosaminoglycan (GAG) which is composed of a chain of alternating sugars including N-acetylgalactosamine and glucuronic acid.
			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/chondroitin-sulfate.html</link>
            <guid isPermaLink="false">57AF47E9-DFAE-42DE-8DA2-6563C4BC26F5</guid>
            <pubDate>Mon, 10 Oct 2011 15:57:59 +0800</pubDate>
        </item>
        <item>
            <title>Astragaloside A | CAS 83207-58-3 | Cyclosiversioside F</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Astragaloside%20A-chemical-structure-s2415.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/astragaloside-a.html" style="color:#062074">Astragaloside A </a>  (Cat No. S2415)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/products/gw3965.html" style="color:#062074">By Research Area</a> » <a href="http://www.selleckchem.com/research_Metabolic-Disease.html" style="color:#062074"> Metabolic Disease </a>  » <a href="http://www.selleckchem.com/products/astragaloside-a.html"style="color:#062074">astragaloside a</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Astragaloside A is a pure small molecular compound isolated from Radix Astragali and is commonly used in the treatment of degenerative bone diseases such as osteoporosis. 
			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/astragaloside-a.html</link>
            <guid isPermaLink="false">07C497B2-1DB9-4B64-A022-81AD00B3C11A</guid>
            <pubDate>Mon, 10 Oct 2011 15:53:32 +0800</pubDate>
        </item>
        <item>
            <title>Flavopiridol hydrochloride | CAS 131740-09-5 | CDK Inhibitor</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Flavopiridol%20hydrochloride-chemical-structure-S2679.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/flavopiridol-hydrochloride.html" style="color:#062074">Flavopiridol hydrochloride</a>  (Cat No. S2679)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Cell-Cycle_Checkpoint.html" style="color:#062074"> Cell Cycle/Checkpoint </a>  » <a href="http://www.selleckchem.com/pathways_CDK.html"style="color:#062074">CDK</a>  » <a href="http://www.selleckchem.com/products/flavopiridol-hydrochloride.html"style="color:#062074">flavopiridol hydrochloride</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Flavopiridol hydrochloride is a pan-cdk inhibitor.
			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/flavopiridol-hydrochloride.html</link>
            <guid isPermaLink="false">D4260CD7-ED6B-404E-B9B5-A55C784FC2CE</guid>
            <pubDate>Mon, 10 Oct 2011 15:48:12 +0800</pubDate>
        </item>
        <item>
            <title>GW3965 | CAS 405911-17-3 | LXR Inhibitor</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/GW3965%20hydrochloride.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/gw3965.html" style="color:#062074">GW3965</a>  (Cat No. S2631)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/products/gw3965.html" style="color:#062074">By Research Area</a> » <a href="http://www.selleckchem.com/research_Cardiovascular-Disease.html" style="color:#062074"> Cardiovascular Disease </a>  » <a href="http://www.selleckchem.com/products/gw3965.html"style="color:#062074">gw3965
</a></div>
							<strong style="color:#062074">Biological Activity:</strong>GW3965 is a synthetic selective, active non-steroidal liver X receptor (LXR) agonist with EC50 of 0.19 and 0.03 μM for hLXRα and hLXRβ, respectively.
			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/gw3965.html</link>
            <guid isPermaLink="false">4210AAFA-7B3D-4CFA-8DD7-B74A74364BB7</guid>
            <pubDate>Thu, 25 Aug 2011 14:23:26 +0800</pubDate>
        </item>
        <item>
            <title>URB597 | CAS 546141-08-6  | FAAH Inhibitor | KDS-4103</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/URB597.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/urb597.html" style="color:#062074">URB597</a>  (Cat No. S2631)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Neuro-Signaling.html" style="color:#062074">Neuro Signaling</a>  » <a href="http://www.selleckchem.com/pathways_FAAH.html"style="color:#062074">FAAH
</a>  » <a href="http://www.selleckchem.com/products/urb597.html"style="color:#062074">urb597</a></div>
							<strong style="color:#062074">Biological Activity:</strong>URB597 is a relatively selective fatty acid amide hydrolase (FAAH) inhibitor with IC50 of 4.6 and 0.5 nM in brain membranes and intact neurons, respectively.
			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/urb597.html</link>
            <guid isPermaLink="false">9698323E-D458-4CFC-90F7-B0B31F571786</guid>
            <pubDate>Thu, 25 Aug 2011 14:19:09 +0800</pubDate>
        </item>
        <item>
            <title>NPS-2143 | CAS 284035-33-2 | CaSR Inhibitor</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/NPS-2143.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/nps-2143.html" style="color:#062074">NPS-2143 </a>  (Cat No. S2633)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Others.html" style="color:#062074">Others</a>  » <a href="http://www.selleckchem.com/pathways_Akt.html"style="color:#062074">AKT</a>  » <a href="http://www.selleckchem.com/pathways_CaSR.html"style="color:#062074">CaSR</a>» <a href="http://www.selleckchem.com/products/nps-2143.html"style="color:#062074">nps-2143</a></div>
							<strong style="color:#062074">Biological Activity:</strong>NPS-2143 is a selective potent calcium ion-sensing receptor antagonist with IC50 of 43 and 41 nM for cytoplasmic Ca2+ concentrations and parathyroid hormone secretion, respectively.
			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/nps-2143.html</link>
            <guid isPermaLink="false">3FE188DB-7427-4E11-8CF5-AF489A9FC127</guid>
            <pubDate>Thu, 25 Aug 2011 14:14:15 +0800</pubDate>
        </item>
        <item>
            <title>DCC-2036 | CAS 1020172-07-9 | Src-bcr-Abl Inhibitor</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/DCC-2036-chemical-structure-S2634.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/dcc-2036.html" style="color:#062074">DCC-2036</a>  (Cat No. S2634)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Angiogenesis_Tyrosine-Kinase.html" style="color:#062074">Angiogenesis/Tyrosine Kinase</a>  » <a href="http://www.selleckchem.com/pathways_Src-bcr-Abl.html"style="color:#062074">Src-bcr-Abl</a>  » <a href="http://www.selleckchem.com/products/dcc-2036.html"style="color:#062074">dcc-2036</a> </div>
							<strong style="color:#062074">Biological Activity:</strong>DCC-2036 is an ABL switch control inhibitor with IC50 of 0.8 and 2 nM for u-ABL1native and p-ABL1native, respectively. 
			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/dcc-2036.html</link>
            <guid isPermaLink="false">C3A749C7-9CBF-455F-A50F-D4A45296F649</guid>
            <pubDate>Thu, 25 Aug 2011 14:08:50 +0800</pubDate>
        </item>
        <item>
            <title>CCT128930 | CAS 885499-61-6 | Akt Inhibitor</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/CCT128930-chemical-structure-S2635.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/cct128930.html" style="color:#062074">CCT128930 </a>  (Cat No. S2635)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_PI3K_Akt_mTOR.html" style="color:#062074">PI3K/Akt/mTOR Pathway</a>  » <a href="http://www.selleckchem.com/pathways_Akt.html"style="color:#062074">AKT</a>  » <a href="http://www.selleckchem.com/products/cct128930.html"style="color:#062074">cct128930
</a></div>
							<strong style="color:#062074">Biological Activity:</strong>CCT128930 is a novel potent ATP-competitive, AKT inhibitor with an IC50 of 6 nM.
			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/cct128930.html</link>
            <guid isPermaLink="false">AA4CFD47-ADAE-4708-BE45-116F2925A0EC</guid>
            <pubDate>Thu, 25 Aug 2011 13:45:09 +0800</pubDate>
        </item>
        <item>
            <title>BMS-806 (BMS 378806) | CAS 357263-13-9  | gp120/CD4 Inhibitor</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/BMS806-BMS-378806-chemical-structure-S2632.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/bms806.html" style="color:#062074">bms806</a>  (Cat No. S2632)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Others.html" style="color:#062074">Others
</a>  » <a href="http://www.selleckchem.com/pathways_gp120_CD4.html"style="color:#062074">gp120/CD4</a>  » <a href="http://www.selleckchem.com/products/bms806.html"style="color:#062074">bms806</a></div>
							<strong style="color:#062074">Biological Activity:</strong>BMS-806 (BMS 378806) is a small molecules gp120/CD4 inhibitor with an IC50 of median 5 nM.
			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/bms806.html</link>
            <guid isPermaLink="false">504BEC9C-D5F3-453B-95B0-26CFD99E6E0A</guid>
            <pubDate>Thu, 25 Aug 2011 13:38:52 +0800</pubDate>
        </item>
        <item>
            <title>A66 | CAS 1166227-08-2  | PI3K Inhibitor</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/A66-chemical-structure-S2636.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/a66.html" style="color:#062074">A66</a>  (Cat No. S2636)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_PI3K_Akt_mTOR.html" style="color:#062074">PI3K/Akt/mTOR Pathway</a>  » <a href=http://www.selleckchem.com/products/a-922500.html"style="color:#062074">a 922500</a>  » <a href=http://www.selleckchem.com/pathways_PI3K.html"style="color:#062074">Mek/pi3k</a>  » <a href="http://www.selleckchem.com/products/a66.html"style="color:#062074">A66</a></div>
							<strong style="color:#062074">Biological Activity:</strong>A66 is a highly specific and selective p110α inhibitor with IC50 of 32,30 and 43 nM for p110α, p110α/E545K, p110α/H1047R, respectively.
			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/a66.html</link>
            <guid isPermaLink="false">451C620B-0DA3-4F3C-9CD2-594B37FE1523</guid>
            <pubDate>Thu, 25 Aug 2011 10:57:20 +0800</pubDate>
        </item>
        <item>
            <title>PNU-120596 | CAS 501925-31-1 | AChR Inhibitor</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/PNU120596-chemical-structure-S2629.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/pnu120596.html" style="color:#062074">PNU-120596</a>  (Cat No. S2629)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Neuro-Signaling.html" style="color:#062074">Neuro Signaling</a>  » <a href="http://www.selleckchem.com/pathways_AChR.html"style="color:#062074">AChR
</a>  » <a href="http://www.selleckchem.com/products/pnu120596.html"style="color:#062074">pnu120596</a></div>
							<strong style="color:#062074">Biological Activity:</strong>PNU-120596 is a potent and selective positive allosteric α7 neuronal nicotinic acetylcholine receptors modulator with an EC50 of 0.2 μM. 
			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/pnu120596.html</link>
            <guid isPermaLink="false">358CDE1F-F30F-462C-8CB2-FE25C632BFFC</guid>
            <pubDate>Thu, 25 Aug 2011 10:52:39 +0800</pubDate>
        </item>
        <item>
            <title>D-87503 | CAS 800394-83-6 | MEK Inhibitor, PI3K Inhibitor</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/D-87503.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/d-87503.html" style="color:#062074">D-87503</a>  (Cat No. S2676)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_PI3K_Akt_mTOR.html" style="color:#062074">PI3K/Akt/mTOR Pathway</a>  » <a href="http://www.selleckchem.com/products/a-922500.html"style="color:#062074">a 922500</a>  » <a href="http://www.selleckchem.com/pathways_PI3K.html"style="color:#062074">Mek/pi3k</a>  » <a href="http://www.selleckchem.com/products/d-87503.html"style="color:#062074">d-87503</a></div>
							<strong style="color:#062074">Biological Activity:</strong>D-87503 is a potent PI3K/Akt/mTOR signaling pathway inhibitor with IC50 of 62nM and 0.76μM for PI3K and Erk2, respectively.
			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/d-87503.html</link>
            <guid isPermaLink="false">B5261F84-4D06-4382-ACAC-BD2F0A915DA5</guid>
            <pubDate>Wed, 24 Aug 2011 15:04:03 +0800</pubDate>
        </item>
        <item>
            <title>D-106669 | CAS 938444-93-0 | PI3K Inhibitor</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/D-106669.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/d-106669.html" style="color:#062074">D-106669</a>  (Cat No. S2675)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_PI3K_Akt_mTOR.html" style="color:#062074">PI3K/Akt/mTOR Pathway</a>  » <a href="http://www.selleckchem.com/products/a-922500.html"style="color:#062074">a 922500</a>  » <a href="http://www.selleckchem.com/pathways_PI3K.html"style="color:#062074">pi3k</a>  » <a href="http://www.selleckchem.com/products/d-106669.html"style="color:#062074">d-106669</a></div>
							<strong style="color:#062074">Biological Activity:</strong>D-106669 is a highly selective PI3K inhibitor with a submicromolar inhibition.
			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/d-106669.html</link>
            <guid isPermaLink="false">1A2C26EA-E051-4FD7-A587-6CFFDA77DEBF</guid>
            <pubDate>Wed, 24 Aug 2011 14:54:56 +0800</pubDate>
        </item>
        <item>
            <title>A 922500 | CAS 959122-11-3</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/A-922500.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/a-922500.html" style="color:#062074">A 922500</a>  (Cat No. S2674)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/researcharea.html" style="color:#062074">By Research Area</a> » <a href="http://www.selleckchem.com/research_Metabolic-Disease.html" style="color:#062074">Metabolic Disease</a>  » <a href="http://www.selleckchem.com/products/a-922500.html"style="color:#062074">a 922500</a></div>
							<strong style="color:#062074">Biological Activity:</strong>A 922500 is a potent and selective diacylglycerol acyltransferase 1 (DGAT-1) inhibitor with IC50 of 7 and 22nM for human and mouse DGAT-1, respectively.
			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/a-922500.html</link>
            <guid isPermaLink="false">A6FC5F5A-818A-4E29-AFCA-D4A02164344D</guid>
            <pubDate>Wed, 24 Aug 2011 11:35:27 +0800</pubDate>
        </item>
        <item>
            <title>Fesoterodine fumarate (Toviaz) | CAS 286930-03-8 | mAChRs Inhibitor | Toviaz</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Fesoterodinefumarate.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/Fesoterodine-fumarate-Toviaz.html" style="color:#062074">Fesoterodine fumarate</a>  (Cat No. S2242)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/researcharea.html" style="color:#062074">By Research Area</a> » <a href="http://www.selleckchem.com/pharmacological_GPCR.html" style="color:#062074">GPCR</a>  » <a href=http://www.selleckchem.com/pathways_mAChRs.html"style="color:#062074">mAChRs</a>» <a href="http://www.selleckchem.com/products/Fesoterodine-fumarate-Toviaz.html"style="color:#062074">Fesoterodine fumarate-Toviaz</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Fesoterodine fumarate (Toviaz) is an antimuscarinic agent and is rapidly de-esterified to its active metabolite 5-hydroxymethyl tolterodine that is a muscarinic receptor antagonist.			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/Fesoterodine-fumarate-Toviaz.html</link>
            <guid isPermaLink="false">41DF4FE3-212C-427C-AEB7-CE69DB8DC347</guid>
            <pubDate>Wed, 18 May 2011 15:06:27 +0800</pubDate>
        </item>
        <item>
            <title>LY 2886721 | CAS N/A | LY2886721</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/LY2886721.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/LY-2886721.html" style="color:#062074">LY 2886721 </a>  (Cat No. S2156)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/researcharea.html" style="color:#062074">By Research Area</a> » <a href="http://www.selleckchem.com/research_Neurological-Disease.html" style="color:#062074">Neurological Disease
</a>  » <a href="http://www.selleckchem.com/products/LY-2886721.html"style="color:#062074">LY 2886721</a></div>
							<strong style="color:#062074">Biological Activity:</strong>LY 2886721 is a novel potent agent that is used to treat Alzheimer’s Disease in preclinical experiments.
						</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/LY-2886721.html</link>
            <guid isPermaLink="false">6EB67742-7A34-4E70-B70C-3F9DED9EC5E4</guid>
            <pubDate>Wed, 18 May 2011 14:44:19 +0800</pubDate>
        </item>
        <item>
            <title>Cortisone acetate (Cortone) | CAS 50-04-4 | Artriona, Biocort Acetate, Cortadren, Incortin, NSC 49420, Scheroson</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Cortisone%20acetate.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/Cortisone-acetate-Cortone.html" style="color:#062074">Cortisone acetate</a>  (Cat No. S2559)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/researcharea.html" style="color:#062074">By Research Area</a> » <a href="http://www.selleckchem.com/research_Immunology.html" style="color:#062074">Immunology</a>  » <a href="http://www.selleckchem.com/products/Cortisone-acetate-Cortone.html"style="color:#062074">Cortisone acetate-Cortone
</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Cortisone acetate (Cortone) is an acetate salt form of cortisone that is a steroid hormone and a glucocorticoid. 			</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/Cortisone-acetate-Cortone.html</link>
            <guid isPermaLink="false">E5146254-5675-4CAA-908B-04F743AB258D</guid>
            <pubDate>Wed, 18 May 2011 14:31:41 +0800</pubDate>
        </item>
        <item>
            <title>Clomifene citrate (Serophene) | CAS 50-41-9 | Estrogen receptor Inhibitor | Clomid, Serophene, Milophene</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Clomifene%20citrate.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href=http://www.selleckchem.com/products/Clomifene-citrate-Serophene.html" style="color:#062074">Clomifene citrate
</a>  (Cat No. S2561)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Hormone.html" style="color:#062074">Hormone</a>  » <a href=http://www.selleckchem.com/pathways_Estrogen-receptor.html"style="color:#062074">Estrogen receptor</a> » <a href=http://www.selleckchem.com/products/Clomifene-citrate-Serophene.html"style="color:#062074">Clomifene citrate</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Clomifene citrate (Serophene) is a selective estrogen receptor modulator.
						</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/Clomifene-citrate-Serophene.html</link>
            <guid isPermaLink="false">045AFCCA-22B8-470E-9DBF-9B944978064C</guid>
            <pubDate>Wed, 18 May 2011 14:21:16 +0800</pubDate>
        </item>
        <item>
            <title>Hydralazine hydrochloride | CAS 304-20-1 | Apresoline</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Hydralazine%20hydrochloride.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href=http://www.selleckchem.com/products/Hydralazine-hydrochloride.html" style="color:#062074">Hydralazine hydrochloride</a>  (Cat No. S2562)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/researcharea.html" style="color:#062074">By Research Area</a> » <a href="http://www.selleckchem.com/research_Cardiovascular-Disease.html" style="color:#062074">Cardiovascular Disease
</a>  » <a href=http://www.selleckchem.com/products/Hydralazine-hydrochloride.html"style="color:#062074">Hydralazine hydrochloride</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Cloxacillin sodium (Cloxacap) is a sodium salt of cloxacillin that is a penicillinase-resistant, acid resistant, semi-synthetic penicillin.
						</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/Hydralazine-hydrochloride.html</link>
            <guid isPermaLink="false">C7DE2956-772A-4901-9696-6BF612260439</guid>
            <pubDate>Wed, 18 May 2011 14:16:35 +0800</pubDate>
        </item>
        <item>
            <title>Cloxacillin sodium (Cloxacap) | CAS 7081-44-9 | Cloxapen, Cloxacap, Orbenin</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Cloxacillin%20sodium.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href=http://www.selleckchem.com/products/Cloxacillin-sodium-Cloxacap.html" style="color:#062074">Cloxacillin sodium</a>  (Cat No. S2564)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/researcharea.html" style="color:#062074">By Research Area</a> » <a href="http://www.selleckchem.com/research_Infection.html" style="color:#062074">Infection</a>  » <a href=http://www.selleckchem.com/products/Cloxacillin-sodium-Cloxacap.html"style="color:#062074">Cloxacillin sodium-Cloxacap</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Cloxacillin sodium (Cloxacap) is a sodium salt of cloxacillin that is a penicillinase-resistant, acid resistant, semi-synthetic penicillin.
						</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/Cloxacillin-sodium-Cloxacap.html</link>
            <guid isPermaLink="false">5B658E6C-5496-4C2F-AFA0-59DC957441C1</guid>
            <pubDate>Wed, 18 May 2011 14:12:21 +0800</pubDate>
        </item>
        <item>
            <title>Isoprenaline hydrochloride | CAS 51-30-9 | adrenergic receptor Inhibitor | Isuprel, Isadrine, Euspiran, Proternol, NSC 37745, NSC 89747</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Isoprenaline%20hydrochloride.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href=http://www.selleckchem.com/products/Isoprenaline-hydrochloride.html" style="color:#062074">Isoprenaline hydrochloride 
</a>  (Cat No. S2566)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_GPCR.html" style="color:#062074">GPCR</a>  » <a href=http://www.selleckchem.com/pathways_adrenergic-receptor.html"style="color:#062074">adrenergic receptor</a> » <a href=http://www.selleckchem.com/products/Isoprenaline-hydrochloride.html"style="color:#062074">Isoprenaline hydrochloride
</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Isoprenaline hydrochloride is a beta-adrenergic agonist. 
						</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/Isoprenaline-hydrochloride.html</link>
            <guid isPermaLink="false">1113164D-CDA4-4F28-905A-D3C320BDC3EE</guid>
            <pubDate>Wed, 18 May 2011 14:02:40 +0800</pubDate>
        </item>
        <item>
            <title>Oxacillin sodium monohydrate &gt;99%(HPLC) | (CAS 7240-38-2) | Order Online | Oxacillin sodium monohydrate</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Oxacillin%20sodium%20monohydrate.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href=http://www.selleckchem.com/products/Oxacillin-sodium-monohydrate.html" style="color:#062074">Oxacillin sodium monohydrate
</a>  (Cat No. S2563)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/researcharea.html" style="color:#062074">By Research Area</a> » <a href="http://www.selleckchem.com/research_Infection.html" style="color:#062074">Infection</a>  » <a href=http://www.selleckchem.com/products/Oxacillin-sodium-monohydrate.html"style="color:#062074">Oxacillin sodium monohydrate</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Oxacillin sodium monohydrate is an antibacterial agent and is a narrow spectrum beta-lactam antibiotic of the penicillin class.
						</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/Oxacillin-sodium-monohydrate.html</link>
            <guid isPermaLink="false">9A52EF13-5FA7-4BA4-9C5C-04001D6B2DD7</guid>
            <pubDate>Thu, 12 May 2011 09:42:15 +0800</pubDate>
        </item>
        <item>
            <title>Alizarin &gt;99%(HPLC) | (CAS 72-48-0) | Order Online | Rubia, alizarin crimson, crimson madder, rose madder, Alizarin</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Tolterodine%20tartrate.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href=http://www.selleckchem.com/products/Alizarin.html" style="color:#062074">Alizarin
</a>  (Cat No. S2526)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/researcharea.html" style="color:#062074">By Research Area</a> » <a href="http://www.selleckchem.com/research_Metabolic-Disease.html" style="color:#062074">Metabolic Disease</a>  » <a href=http://www.selleckchem.com/products/Alizarin.html"style="color:#062074">Alizarin</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Alizarin (Rubia, Rezza, alizarin crimson, crimson madder) is an organic compound and an important prominent dye.

						</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/Alizarin.html</link>
            <guid isPermaLink="false">8540F66D-5DBA-4FB4-898F-C4258F322652</guid>
            <pubDate>Fri, 6 May 2011 10:23:00 +0800</pubDate>
        </item>
        <item>
            <title>Tiotropium Bromide(Spiriva, BA 679BR) &gt;99%(HPLC) | (CAS 136310-93-5) | Muscarinic receptor Inhibitor | Spiriva, Tiova, BA 679BR, Tiopropium, Tiotropium Bromide(Spiriva, BA 679BR)</title>
            <description>
                <![CDATA[<table width="100%" border=0 cellpadding=1 bordercolorlight="#f0f0f0" bordercolordark="#a0a0a0" cellspacing=2>
<tr valign=top>
<td width=367 valign=middle><img alt="src="http://www.selleckchem.com/pic/digi/Tiotropium%20Bromide.gif" style="margin-right:20px" " src="http://www.selleckchem.com/pic/digi/Tiotropium%20Bromide.gif"><br />
</td>
<td valign=middle><b>Product:</b><a href="http://www.selleckchem.com/products/Tiotropium-Bromide-Spiriva.html"" style="color:#062074"> Tiotropium Bromide(Spiriva, BA 679BR) </a>(Cat No. S2546)<br />
<b>Category:</b><a href="http://www.selleckchem.com/pharmacologicalact.htmll" style="color:#062074"> By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_GPCR.html" style="color:#062074">GPCR</a> » <a href="http://www.selleckchem.com/pathways_Muscarinic-receptor.html"style="color:#062074"">Muscarinic receptor</a>» <a href="http://www.selleckchem.com/products/Tiotropium-Bromide-Spiriva.html"style="color:#062074"">Tiotropium Bromide-Spiriva</a><br />
<b>Biological Activity:</b>Tiotropium Bromide(Spiriva, BA 679BR) is a synthetic quaternary ammonium antimuscarinic agent and is a muscarinic receptor antagonist. <br />
</td>
</tr>
</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/Tiotropium-Bromide-Spiriva.html</link>
            <guid isPermaLink="false">D1A27870-39AB-486C-AF4E-43CEAA7D5AE6</guid>
            <pubDate>Fri, 6 May 2011 10:18:12 +0800</pubDate>
        </item>
        <item>
            <title>Tiotropium Bromide monohydrate &gt;99%(HPLC) | (CAS 139404-48-1) | Muscarinic receptor Inhibitor | Tiotropium Bromide monohydrate</title>
            <description>
                <![CDATA[<table width="100%" border=0 cellpadding=1 bordercolorlight="#f0f0f0" bordercolordark="#a0a0a0" cellspacing=2>
<tr valign=top>
<td width=367 valign=middle><img alt="src="http://www.selleckchem.com/pic/digi/Tiotropium%20Bromide%20hydrate.gif" style="margin-right:20px" " src="http://www.selleckchem.com/pic/digi/Tiotropium%20Bromide%20hydrate.gif"><br />
</td>
<td valign=middle><b>Product:</b><a href="http://www.selleckchem.com/products/Tiotropium-Bromide-monohydrate.html"" style="color:#062074"> Tiotropium Bromide monohydrate </a>(Cat No. S2549)<br />
<b>Category:</b><a href="http://www.selleckchem.com/pharmacologicalact.htmll" style="color:#062074"> By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_GPCR.html" style="color:#062074">GPCR</a> » <a href="http://www.selleckchem.com/pathways_Muscarinic-receptor.html"style="color:#062074"">Muscarinic receptor</a>» <a href="http://www.selleckchem.com/products/Tiotropium-Bromide-monohydrate.html"style="color:#062074"">Tiotropium Bromide monohydrate</a><br />
<b>Biological Activity:</b>Tiotropium Bromide monohydrate is a monohydrate of tiotropium bromide (Spiriva; Tiova; BA 679BR; tiopropium) that is an anticholinergic and bronchodilator and a muscarinic receptor antagonist. <br />
</td>
</tr>
</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/Tiotropium-Bromide-monohydrate.html</link>
            <guid isPermaLink="false">BD4A47B8-B409-4A16-8331-7244BAEE38CF</guid>
            <pubDate>Fri, 6 May 2011 10:15:13 +0800</pubDate>
        </item>
        <item>
            <title>Trospium chloride (Sanctura) &gt;99%(HPLC) | (CAS 10405-02-4) | Muscarinic receptor Inhibitor | Sanctura, Trospium chloride (Sanctura)</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Trospium%20chloride.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href=http://www.selleckchem.com/products/Trospium-chloride-Sanctura.html" style="color:#062074">Trospium chloride (Sanctura)
</a>  (Cat No. S2549)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.htmll" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_GPCR.html" style="color:#062074">GPCR</a>  » <a href=http://www.selleckchem.com/pathways_Muscarinic-receptor.html"style="color:#062074">Muscarinic receptor</a>» <a href=http://www.selleckchem.com/products/Trospium-chloride-Sanctura.html"style="color:#062074">Trospium chloride-Sanctura</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Trospium chloride (Sanctura) is a competitive muscarinic cholinergic receptor antagonist. 

						</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/Trospium-chloride-Sanctura.html</link>
            <guid isPermaLink="false">606A5A79-92A3-4427-9B8C-A6B0837AAAD0</guid>
            <pubDate>Fri, 6 May 2011 10:11:44 +0800</pubDate>
        </item>
        <item>
            <title>Tolterodine tartrate (Detrol LA) &gt;99%(HPLC) | (CAS 124937-52-6) | Muscarinic receptor Inhibitor | Detrol LA, Kabi-2234, PNU-200583E, Tolterodine tartrate (Detrol LA)</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Tolterodine%20tartrate.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href=http://www.selleckchem.com/products/Tolterodine-tartrate-Detrol-LA.html" style="color:#062074">Tolterodine tartrate-Detrol LA
</a>  (Cat No. S2550)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.htmll" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_GPCR.html" style="color:#062074">GPCR</a>  » <a href=http://www.selleckchem.com/pathways_Muscarinic-receptor.html"style="color:#062074">Muscarinic receptor</a>» <a href=http://www.selleckchem.com/products/Tolterodine-tartrate-Detrol-LA.html"style="color:#062074">Tolterodine tartrate-Detrol LA</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Tolterodine tartrate (Detrol LA) is a tartrate salt of tolterodine that is a competitive muscarinic receptor antagonist.

						</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/Tolterodine-tartrate-Detrol-LA.html</link>
            <guid isPermaLink="false">D15F10FC-02E9-483F-A024-E18781627C79</guid>
            <pubDate>Fri, 6 May 2011 10:06:49 +0800</pubDate>
        </item>
        <item>
            <title>Azelastine hydrochloride (Astelin) &gt;99%(HPLC) | (CAS 79307-93-0) | histamine Inhibitor | Allergodil, Rhinolast, Astelin, Optilas, Optivar, Azelastine hydrochloride (Astelin)</title>
            <description>
                <![CDATA[<table width="100%" border=0 cellpadding=1 bordercolorlight="#f0f0f0" bordercolordark="#a0a0a0" cellspacing=2>
<tr valign=top>
<td width=367 valign=middle><img alt="src="http://www.selleckchem.com/pic/digi/Azelastine%20hydrochloride.gif" style="margin-right:20px" " src="http://www.selleckchem.com/pic/digi/Azelastine%20hydrochloride.gif"><br />
</td>
<td valign=middle><b>Product:</b><a href="http://www.selleckchem.com/products/Azelastine-hydrochloride-Astelin.html"" style="color:#062074"> Azelastine hydrochloride (Astelin)</a> (Cat No. S2552)<br />
<b>Category:</b><a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074"> By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Neuro-Signaling.html" style="color:#062074">Neuro Signaling</a> » <a href="http://www.selleckchem.com/pathways_histamine.html"style="color:#062074"">histamine</a> » <a href="http://www.selleckchem.com/products/Azelastine-hydrochloride-Astelin.html"style="color:#062074"">Azelastine hydrochloride-Astelin</a><br />
<b>Biological Activity:</b>Azelastine hydrochloride (Astelin) is a potent, second-generation, selective, histamine antagonist. <br />
</td>
</tr>
</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/Azelastine-hydrochloride-Astelin.html</link>
            <guid isPermaLink="false">BC7FF3F4-AC67-415F-B781-002EA19CDFB8</guid>
            <pubDate>Fri, 6 May 2011 09:59:26 +0800</pubDate>
        </item>
        <item>
            <title>5-Aminolevulinic acid hydrochloride &gt;99%(HPLC) | (CAS 5451-09-2) | Order Online | Levulan, ALA, 5-Aminolevulinic acid hydrochloride</title>
            <description>
                <![CDATA[<table width="100%" border=0 cellpadding=1 bordercolorlight="#f0f0f0" bordercolordark="#a0a0a0" cellspacing=2>
<tr valign=top>
<td width=367 valign=middle><img alt="src="http://www.selleckchem.com/pic/digi/5-Aminolevulinic%20acid%20hydrochloride.gif" style="margin-right:20px" " src="http://www.selleckchem.com/pic/digi/5-Aminolevulinic%20acid%20hydrochloride.gif"><br />
</td>
<td valign=middle><b>Product:</b><a href="http://www.selleckchem.com/products/5-Aminolevulinic-acid-hydrochloride.html"" style="color:#062074"> 5-Aminolevulinic acid hydrochloride</a> (Cat No. S2553)<br />
<b>Category:</b><a href="http://www.selleckchem.com/researcharea.html"" style="color:#062074"> By Research Area</a> » <a href="http://www.selleckchem.com/research_chemotherapeutic-agent.html" style="color:#062074">chemotherapeutic agent</a> » <a href="http://www.selleckchem.com/products/5-Aminolevulinic-acid-hydrochloride.html"style="color:#062074"">5-Aminolevulinic acid hydrochloride</a><br />
<b>Biological Activity:</b>5-Aminolevulinic acid is an intermediate in heme biosynthesis in the body and the universal precursor of tetrapyrroles, such as chlorophyll and heme. <br />
</td>
</tr>
</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/5-Aminolevulinic-acid-hydrochloride.html</link>
            <guid isPermaLink="false">271C39F4-70BE-4980-AD16-5D31E0519FFF</guid>
            <pubDate>Fri, 6 May 2011 09:54:10 +0800</pubDate>
        </item>
        <item>
            <title>Daphnetin &gt;99%(HPLC) | (CAS 486-35-1) | Order Online | Daphnetin</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Daphnetin.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href=http://www.selleckchem.com/products/Daphnetin.html" style="color:#062074">Daphnetin</a>  (Cat No. S2554)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/researcharea.html" style="color:#062074">By Research Area</a> » <a href="http://www.selleckchem.com/research_Others.html" style="color:#062074">Others</a>  » <a href=http://www.selleckchem.com/products/Daphnetin.html"style="color:#062074">Daphnetin</a></div>
							<strong style="color:#062074">Biological Activity:</strong>It is also a chelator and an antioxidant. In vitro, daphnetin causes a 50% inhibition (IC50) of 3H-hypoxanthine incorporation by Plasmodium falciparum at concentrations between 25 and 40 µM.

						</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/Daphnetin.html</link>
            <guid isPermaLink="false">2D3659C7-261A-4268-9C0D-3FD5D5BEAD4F</guid>
            <pubDate>Fri, 6 May 2011 09:40:29 +0800</pubDate>
        </item>
        <item>
            <title>Clarithromycin (Biaxin, Klacid) &gt;99%(HPLC) | (CAS 81103-11-9) | DNA/RNA Inhibitor | Crixan, Klaricid, Klabax, Claripen, Clarem, Claridar, Fromilid, Clacid, Clacee, Vikrol, Infex, Clari, Clarithromycin (Biaxin, Klacid)</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Clarithromycin.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href=http://www.selleckchem.com/products/Clarithromycin-Biaxin,-Klacid.html" style="color:#062074">Clarithromycin (Biaxin, Klacid)</a>  (Cat No. S2555)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href=http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Cell-Cycle_Checkpoint.html" style="color:#062074">Cell Cycle/Checkpoint
</a>  » <a href=http://www.selleckchem.com/pathways_DNA_RNA.html"style="color:#062074">DNA/RNA
</a>» <a href=http://www.selleckchem.com/products/Clarithromycin-Biaxin,-Klacid.html"style="color:#062074">Clarithromycin-Biaxin, Klacid
Clarithromycin-Biaxin, Klacid</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Clarithromycin (Biaxin, Klacid) is a macrolide antibiotic and a CYP3A4 substrate and inhibitor.
						</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/Clarithromycin-Biaxin,-Klacid.html</link>
            <guid isPermaLink="false">5CF1B608-1A17-4D3A-A75B-137ABF222381</guid>
            <pubDate>Fri, 6 May 2011 09:35:30 +0800</pubDate>
        </item>
        <item>
            <title>Acetanilide (Antifebrin) &gt;99%(HPLC) | (CAS 103-84-4) | Order Online | N-phenylacetamide, Acetanil, Acetamidobenzene, Acetylaniline, NSC 7636, Acetanilide (Antifebrin)</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Acetanilide.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href=http://www.selleckchem.com/products/Acetanilide-Antifebrin.html" style="color:#062074">Acetanilide (Antifebrin)</a>  (Cat No. S2538)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/researcharea.html" style="color:#062074">By Research Area</a> » <a href="http://www.selleckchem.com/research_Neurological-Disease.html" style="color:#062074">Neurological Disease
</a>  » <a href=http://www.selleckchem.com/products/Acetanilide-Antifebrin.html"style="color:#062074">Acetanilide-Antifebrin
</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Acetanilide (Antifebrin) is an aniline derivative and has possess analgesic. 
						</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/Acetanilide-Antifebrin.html</link>
            <guid isPermaLink="false">B1986A17-89FE-4F1D-B0F1-D8A2487B0847</guid>
            <pubDate>Mon, 25 Apr 2011 15:26:30 +0800</pubDate>
        </item>
        <item>
            <title>Lomefloxacin hydrochloride (Maxaquin) &gt;99%(HPLC) | (CAS 98079-52-8) | Order Online | Maxaquin, Okacyn, Uniquin, , Lomefloxacin hydrochloride (Maxaquin)</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Lomefloxacin%20hydrochloride.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href=http://www.selleckchem.com/products/Lomefloxacin-hydrochloride-Maxaquin.html" style="color:#062074">Lomefloxacin hydrochloride-Maxaquin</a>  (Cat No. S2539)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/researcharea.html" style="color:#062074">By Research Area</a> » <a href="http://www.selleckchem.com/research_Infection.html" style="color:#062074">Infection</a>  » <a href=http://www.selleckchem.com/products/Lomefloxacin-hydrochloride-Maxaquin.html"style="color:#062074">Lomefloxacin hydrochloride-Maxaquin</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Lomefloxacin hydrochloride (Maxaquin) is a hydrochloride salt of lomefloxacin and is a fluoroquinolone antibiotic.
						</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/Lomefloxacin-hydrochloride-Maxaquin.html</link>
            <guid isPermaLink="false">DF45D9CD-521D-4C7D-9721-521BA08BDCE3</guid>
            <pubDate>Mon, 25 Apr 2011 15:09:02 +0800</pubDate>
        </item>
        <item>
            <title>Riboflavin (Vitamin B2) &gt;99%(HPLC) | (CAS 83-88-5) | Order Online | Vitamin B2, E101, Riboflavin (Vitamin B2)</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Riboflavin.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href=http://www.selleckchem.com/products/Riboflavin-Vitamin-B2.html" style="color:#062074">Riboflavin (Vitamin B2) </a>  (Cat No. S2540)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/researcharea.html" style="color:#062074">By Research Area</a> » <a href="http://www.selleckchem.com/research_Metabolic-Disease.html" style="color:#062074">Metabolic Disease</a>  » <a href=http://www.selleckchem.com/products/Riboflavin-Vitamin-B2.html"style="color:#062074">Riboflavin-Vitamin B2
</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Riboflavin (vitamin B2) is an easily absorbed micronutrient with a key role in maintaining health in humans and other animals.
						</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/Riboflavin-Vitamin-B2.html</link>
            <guid isPermaLink="false">11286600-F5F4-4444-8D9D-2CA3C4D4B9E3</guid>
            <pubDate>Mon, 25 Apr 2011 14:55:19 +0800</pubDate>
        </item>
        <item>
            <title>Clomipramine hydrochloride (Anafranil) &gt;99%(HPLC) | (CAS 17321-77-6) | Reuptake inhibitor Inhibitor | Anafranil, Clomipramine hydrochloride (Anafranil)</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Clomipramine%20hydrochloride.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href=http://www.selleckchem.com/products/Clomipramine-hydrochloride-Anafranil.html" style="color:#062074">Clomipramine hydrochloride </a>  (Cat No. S2541)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/products/Clomipramine-hydrochloride-Anafranil.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Neuro-Signaling.html" style="color:#062074">Neuro Signaling</a>  » <a href=http://www.selleckchem.com/pathways_Reuptake-inhibitor.html"style="color:#062074">Reuptake inhibitor
</a> » <a href=http://www.selleckchem.com/products/Clomipramine-hydrochloride-Anafranil.html"style="color:#062074">Clomipramine hydrochloride-Anafranil</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Maprotiline hydrochloride (Deprilept, Ludiomil, Psymion) is a selective noradrenalin re-uptake inhibitor and a tetracyclic antidepressant.
						</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/Clomipramine-hydrochloride-Anafranil.html</link>
            <guid isPermaLink="false">0FF9BE44-235F-4CF5-9AD5-719673F1C77F</guid>
            <pubDate>Mon, 25 Apr 2011 14:39:30 +0800</pubDate>
        </item>
        <item>
            <title>Phenformin hydrochloride &gt;99%(HPLC) | (CAS 834-28-6) | Order Online | Phenformin hydrochloride</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Phenformin%20hydrochloride.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href=http://www.selleckchem.com/products/Ceftiofur-hydrochloride.html" style="color:#062074">Phenformin hydrochloride </a>  (Cat No. S2542)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/researcharea.html" style="color:#062074">By Research Area</a> » <a href="http://www.selleckchem.com/research_Immunology.html" style="color:#062074">Immunology</a>  » <a href=http://www.selleckchem.com/products/Phenformin-hydrochloride.html"style="color:#062074">Phenformin hydrochloride</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Phenformin hydrochloride is a hydrochloride salt of phenformin that is an anti-diabetic drug from the biguanide class.
						</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/Phenformin-hydrochloride.html</link>
            <guid isPermaLink="false">2CEA361E-BE81-4737-BC15-77F523B86D22</guid>
            <pubDate>Mon, 25 Apr 2011 14:29:58 +0800</pubDate>
        </item>
        <item>
            <title>Ceftiofur hydrochloride &gt;99%(HPLC) | (CAS 103980-44-5) | Order Online | Ceftiofur hydrochloride</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Ceftiofur%20hydrochloride.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href=http://www.selleckchem.com/products/Ceftiofur-hydrochloride.html" style="color:#062074">Ceftiofur hydrochloride</a>  (Cat No. S2543)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/researcharea.html" style="color:#062074">By Research Area</a> » <a href="http://www.selleckchem.com/research_Infection.html" style="color:#062074">Infection</a>  » <a href=http://www.selleckchem.com/products/Ceftiofur-hydrochloride.html"style="color:#062074">Ceftiofur hydrochloride</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Ceftiofur hydrochloride is a hydrochloride of ceftiofur that is a broad spectrum cephalosporin.
						</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/Ceftiofur-hydrochloride.html</link>
            <guid isPermaLink="false">1A7560A7-6322-4AEE-912C-8225A087190A</guid>
            <pubDate>Mon, 25 Apr 2011 14:19:46 +0800</pubDate>
        </item>
        <item>
            <title>Cefprozil hydrate (Cefzil) &gt;99%(HPLC) | (CAS 121123-17-9 ) | Order Online | Cefprozil, Cefzil, Cefprozil hydrate (Cefzil)</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Cefprozil%20hydrate.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href=http://www.selleckchem.com/products/Cefprozil-hydrate-Cefzil.html" style="color:#062074">Cefprozil hydrate (Cefzil)</a>  (Cat No. S2544)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/researcharea.html" style="color:#062074">By Research Area</a> » <a href="http://www.selleckchem.com/research_Infection.html" style="color:#062074">Infection</a>  » <a href=http://www.selleckchem.com/products/Cefprozil-hydrate-Cefzil.html"style="color:#062074">Cefprozil hydrate-Cefzil
</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Cefprozil hydrate (Cefzil) is a second-generation cephalosporin type antibiotic. 
						</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/Cefprozil-hydrate-Cefzil.html</link>
            <guid isPermaLink="false">9E273E79-3CA0-4352-A620-A646FCE28732</guid>
            <pubDate>Mon, 25 Apr 2011 14:13:18 +0800</pubDate>
        </item>
        <item>
            <title>TAME &gt;99%(HPLC) | (CAS 901-47-3) | APC Inhibitor | TAME</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Betanin.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href=http://www.selleckchem.com/products/Betanin.html" style="color:#062074">Betanin</a>  (Cat No. S2414)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/researcharea.html" style="color:#062074">By Research Area</a> » <a href="http://www.selleckchem.com/research_chemotherapeutic-agent.html" style="color:#062074">chemotherapeutic agent
</a>  » <a href=http://www.selleckchem.com/products/Betanin.html"style="color:#062074">Betanin</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Betalain is a kind of water-soluble nitrogenous vacuolar pigment and a new class of dietary cationized antioxidants with an IC50 of 40 μM in the treatment of the proliferation of K562 cells.
						</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/TAME.html</link>
            <guid isPermaLink="false">28FB6722-93F0-4468-A301-3ED402103C48</guid>
            <pubDate>Wed, 20 Apr 2011 17:18:01 +0800</pubDate>
        </item>
        <item>
            <title>Betanin &gt;99%(HPLC) | (CAS 7659-95-2) | Order Online | Betanin</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/TAME.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href=http://www.selleckchem.com/products/TAME.html" style="color:#062074">TAME</a>  (Cat No. S2225)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Cell-Cycle_Checkpoint.html" style="color:#062074">Cell Cycle/Checkpoint
</a>  » <a href=http://www.selleckchem.com/pathways_APC.html"style="color:#062074">APC</a> » <a href="http://www.selleckchem.com/products/TAME.html" style="color:#062074">TAME</a></div>
							<strong style="color:#062074">Biological Activity:</strong>TAME is a small molecule anaphase-promoting complex/cyclosome (APC) inhibitor with an IC50 of 12 μM.
						</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/Betanin.html</link>
            <guid isPermaLink="false">06D8D599-574A-4C6C-A9FC-9DBBF9AA1FC5</guid>
            <pubDate>Wed, 20 Apr 2011 16:49:40 +0800</pubDate>
        </item>
        <item>
            <title>Telatinib (BAY 57-9352) &gt;99%(HPLC) | (CAS 332012-40-5) | c-Kit Inhibitor | VEGFR-PDGFR Inhibitor | BAY 57-9352, Telatinib (BAY 57-9352)</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Telatinib%20(BAY%2057-9352).gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href=http://www.selleckchem.com/products/Telatinib-BAY-57-9352.html" style="color:#062074">Telatinib-BAY 57-9352</a>  (Cat No. S2231)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pathways_c-Kit.html" style="color:#062074">c-Kit /  <a href="http://www.selleckchem.com/pathways_VEGFR-PDGFR.html" style="color:#062074">VEGFR-PDGFR</a>  » <a href=http://www.selleckchem.com/products/Telatinib-BAY-57-9352.html"style="color:#062074">Telatinib-BAY 57-9352
</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Telatinib (BAY 57-9352) is an orally available, potent multitargeted VEGFR-2, VEGFR-3, PDGFR-β and c-Kit tyrosine kinases inhibitor with an IC50 of 19 nM for the inhibition of VEGFR-2 autophosphorylation.
						</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/Ketanserin-Vulketan-Gel.html</link>
            <guid isPermaLink="false">9E11DF19-E7CB-4283-8B1F-27A857657F49</guid>
            <pubDate>Wed, 20 Apr 2011 16:31:25 +0800</pubDate>
        </item>
        <item>
            <title>TAME &gt;99%(HPLC) | (CAS 901-47-3) | APC Inhibitor | TAME</title>
            <link>http://www.selleckchem.com/products/Ketanserin-Vulketan-Gel.html</link>
            <guid isPermaLink="false">B86E7933-028A-40E6-99D8-193620201D5A</guid>
            <pubDate>Wed, 20 Apr 2011 16:15:16 +0800</pubDate>
        </item>
        <item>
            <title>Esomeprazole sodium (Nexium I.V.) &gt;99%(HPLC) | (CAS 161796-78-7) | proton pump Inhibitor | Sompraz, Zoleri, Lucen, Esopral, Axagon, Nexiam, Esomeprazole sodium (Nexium I.V.)</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Esomeprazole%20sodium.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href=http://www.selleckchem.com/products/Esomeprazole-sodium-Nexium-I.V..html" style="color:#062074">Esomeprazole sodium-Nexium I.V.
</a>  (Cat No. S2233)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Others.html" style="color:#062074">Others</a>  » <a href=http://www.selleckchem.com/pathways_proton-pump.html"style="color:#062074">proton pump</a>» <a href=http://www.selleckchem.com/products/Esomeprazole-sodium-Nexium-I.V..html"style="color:#062074">Esomeprazole sodium-Nexium I.V.</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Esomeprazole sodium (Nexium I.V.) is a sodium salt of esomeprazole that is a potent proton pump inhibitor with an IC50 of 0.076 mg/kg.

						</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/Esomeprazole-sodium-Nexium-I.V..html</link>
            <guid isPermaLink="false">E4A53B26-5093-4E2F-ADFD-B3C4AFC41DA4</guid>
            <pubDate>Wed, 20 Apr 2011 16:06:09 +0800</pubDate>
        </item>
        <item>
            <title>BI6727 (Volasertib) &gt;99%(HPLC) | (CAS 755038-65-4) | PLK Inhibitor | Volasertib, BI6727 (Volasertib)</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/BI%206727.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href=http://www.selleckchem.com/products/BI6727-Volasertib.html" style="color:#062074">BI6727 (Volasertib)</a>  (Cat No. S2235)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Cell-Cycle_Checkpoint.html" style="color:#062074">Cell Cycle/Checkpoint</a>  » <a href=http://www.selleckchem.com/pathways_PLK.html"style="color:#062074">PLK</a>» <a href=http://www.selleckchem.com/products/BI6727-Volasertib.html"style="color:#062074">BI6727-Volasertib</a></div>
							<strong style="color:#062074">Biological Activity:</strong>BI 6727 is a highly potent Polo-like kinase inhibitor with an IC50 of 0 .87 nM.

						</td>
					</tr>
					</table>]]>
            </description>
            <link>http://69.65.42.27/products/BI6727-Volasertib.html</link>
            <guid isPermaLink="false">633B5606-EB8B-433C-9AC3-28A386FEC57D</guid>
            <pubDate>Wed, 20 Apr 2011 15:53:56 +0800</pubDate>
        </item>
        <item>
            <title>CAL-101 &gt;99%(HPLC) | (CAS 870281-82-6) | PI3K Inhibitor | CAL101, CAL-101</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Eltrombopag.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/Eltrombopag-SB-497115-GR.html" style="color:#062074">Eltrombopag (SB-497115-GR)</a>  (Cat No. S2226)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_PI3K_Akt_mTOR.html" style="color:#062074">PI3K/Akt/mTOR</a>  » <a href=http://www.selleckchem.com/pathways_PI3K.html"style="color:#062074">PI3K</a>» <a href="http://www.selleckchem.com/products/CAL-101.html">CAL-101</a></div>
							<strong style="color:#062074">Biological Activity:</strong>CAL-101 is a potent PI3K p110δ inhibitor with an IC50 of 65 nM.


						</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/CAL-101.html</link>
            <guid isPermaLink="false">5D65AD11-1B85-4BFE-95F6-EF3AC6E0528A</guid>
            <pubDate>Fri, 15 Apr 2011 16:40:42 +0800</pubDate>
        </item>
        <item>
            <title>Eltrombopag (SB-497115-GR) &gt;99%(HPLC) | (CAS 496775-61-2) | TpoR Inhibitor | SB-497115-GR, Revolade, Promacta, Eltrombopag (SB-497115-GR)</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Eltrombopag.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/Eltrombopag-SB-497115-GR.html" style="color:#062074">Eltrombopag (SB-497115-GR)</a>  (Cat No. S2229)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Hormone.html" style="color:#062074">Hormone</a>  » <a href="http://www.selleckchem.com/pathways_TpoR.html"style="color:#062074">TpoR</a>» <a href="http://www.selleckchem.com/products/Eltrombopag-SB-497115-GR.html">Eltrombopag-SB-497115-GR
</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Eltrombopag (SB-497115-GR, Promacta, Revolade) is a small molecule agonist of the c-mpl (TpoR) receptor with an IC50 of 0.69 μM for the inhibition of hERG K+ channel tail current. 


						</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/Eltrombopag-SB-497115-GR.html</link>
            <guid isPermaLink="false">F279E1A0-6E01-473D-AA1A-53D86EE68998</guid>
            <pubDate>Fri, 15 Apr 2011 16:32:45 +0800</pubDate>
        </item>
        <item>
            <title>VX-765 &gt;99%(HPLC) | (CAS 273404-37-8) | Caspase Inhibitor | VX765, VX-765</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/VX%20765.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/VX-765.html" style="color:#062074">SB590885</a>  (Cat No. S2228)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Apoptosis.html" style="color:#062074">Apoptosis</a>  » <a href="http://www.selleckchem.com/pathways_Caspase.html"style="color:#062074">Caspase</a>» <a href="http://www.selleckchem.com/products/VX-765.html">VX-765</a></div>
							<strong style="color:#062074">Biological Activity:</strong>VX-765 is a novel and irreversible IL-converting enzyme/caspase-1 inhibitor with an IC50 of 0.8 nM.


						</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/VX-765.html</link>
            <guid isPermaLink="false">19E48720-6C2E-44D2-B8EC-6A9F2055CDC7</guid>
            <pubDate>Fri, 15 Apr 2011 16:19:14 +0800</pubDate>
        </item>
        <item>
            <title>SB590885 &gt;99%(HPLC) | (CAS 405554-55-4 ) | B-Raf Inhibitor | SB 590885, SB590885</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/SB%20590885.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/SB590885.html" style="color:#062074">SB590885</a>  (Cat No. S2220)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_MAPK.html" style="color:#062074">MAPK</a>  » <a href="http://www.selleckchem.com/pathways_B-Raf.html"style="color:#062074">B-Raf</a>» <a href="http://www.selleckchem.com/products/SB590885.html"style="color:#062074">SB590885
</a></div>
							<strong style="color:#062074">Biological Activity:</strong>SB-590885 stabilizes the oncogenic B-Raf kinase domain in an active configuration, which is distinct from the previously reported mechanism of action of the multi-kinase inhibitor, BAY43-9006.


						</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/SB590885.html</link>
            <guid isPermaLink="false">AB019533-5A14-4E12-8F23-EDE337D868C4</guid>
            <pubDate>Fri, 15 Apr 2011 16:14:38 +0800</pubDate>
        </item>
        <item>
            <title>Cyt387 &gt;99%(HPLC) | (CAS 1056634-68-4) | JAK Inhibitor | CYT 11387, Cyt-387, Cyt387</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/CYT%20387.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/Cyt387.html" style="color:#062074">Cyt387</a>  (Cat No. S2219)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Jak_Stat.html" style="color:#062074">Jak/Stat</a>  » <a href="http://www.selleckchem.com/pathways_JAK.html"style="color:#062074">JAK</a>» <a href="http://www.selleckchem.com/products/Cyt387.html"style="color:#062074">Cyt387
</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Cyt387 is an ATP-competitive small molecule JAK1/JAK2 inhibitor with IC50 of 11 and 18 nM for JAK1 and JAK2, respectively.

						</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/Cyt387.html</link>
            <guid isPermaLink="false">27BB4556-0B21-43A3-982A-E1BD94E77568</guid>
            <pubDate>Fri, 15 Apr 2011 16:09:21 +0800</pubDate>
        </item>
        <item>
            <title>PP242 &gt;99%(HPLC) | (CAS 1092351-67-1) | mTOR Inhibitor | PP 242, PP242</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/PP%20242.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/PP242.html" style="color:#062074">PP242</a>  (Cat No. S2218)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_PI3K_Akt_mTOR.html" style="color:#062074">PI3K/Akt/mTOR</a>  » <a href="http://www.selleckchem.com/pathways_mTOR.html"style="color:#062074">mTOR</a>» <a href="http://www.selleckchem.com/products/PP242.html"style="color:#062074">PP242
</a></div>
							<strong style="color:#062074">Biological Activity:</strong>PP242 is a novel potent and selective mTOR inhibitor with an IC50 of 8 nM.
						</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/PP242.html</link>
            <guid isPermaLink="false">A48D82B2-78B4-4A1E-AB66-D51D583F57E5</guid>
            <pubDate>Fri, 15 Apr 2011 15:51:36 +0800</pubDate>
        </item>
        <item>
            <title>Nattokinase &gt;99%(HPLC) | (CAS 133876-92-3 ) | Order Online | Nattokinase</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Secnidazole.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/Secnidazole-Flagentyl.html" style="color:#062074">Secnidazole (Flagentyl)</a>  (Cat No. S2537)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/researcharea.html" style="color:#062074">By Research Area</a> » <a href="http://www.selleckchem.com/research_Infection.html" style="color:#062074">Infection</a>  » <a href="http://www.selleckchem.com/products/Secnidazole-Flagentyl.html"style="color:#062074">Secnidazole-Flagentyl</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Secnidazole (Flagentyl) is a nitroimidazole anti-infective. Secnidazole (Flagentyl) is effective in the treatment of dientamoebiasis. 

						</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/Nattokinase.html</link>
            <guid isPermaLink="false">0A66D610-C873-4927-9DF5-18D31058FAF1</guid>
            <pubDate>Fri, 15 Apr 2011 15:41:30 +0800</pubDate>
        </item>
        <item>
            <title>Secnidazole (Flagentyl) &gt;99%(HPLC) | (CAS 3366-95-8) | Order Online | PM 185184; RP 14539; Sindose; Secnil, Secnidazole (Flagentyl)</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Secnidazole.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/Secnidazole-Flagentyl.html" style="color:#062074">Secnidazole (Flagentyl)</a>  (Cat No. S2537)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/researcharea.html" style="color:#062074">By Research Area</a> » <a href="http://www.selleckchem.com/research_Infection.html" style="color:#062074">Infection</a>  » <a href="http://www.selleckchem.com/products/Secnidazole-Flagentyl.html"style="color:#062074">Secnidazole-Flagentyl</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Secnidazole (Flagentyl) is a nitroimidazole anti-infective. Secnidazole (Flagentyl) is effective in the treatment of dientamoebiasis. 

						</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/Secnidazole-Flagentyl.html</link>
            <guid isPermaLink="false">67B0C0A1-7973-456B-8D85-402B137CD4E2</guid>
            <pubDate>Fri, 15 Apr 2011 15:37:11 +0800</pubDate>
        </item>
        <item>
            <title>Miconazole (Monistat) &gt;99%(HPLC) | (CAS 22916-47-8) | Order Online | Daktarin IV; MJR 1762; Monistat IV; NSC 170986; R 18134; Zimybase, Miconazole (Monistat)</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Miconazole.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/Miconazole-Monistat.html" style="color:#062074">Miconazole</a>  (Cat No. S2536)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/researcharea.html" style="color:#062074">By Research Area</a> » <a href="http://www.selleckchem.com/research_Infection.html" style="color:#062074">Infection</a>  » <a href="http://www.selleckchem.com/products/Miconazole-Monistat.html"style="color:#062074">Miconazole-Monistat
</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Miconazole (Monistat) is an imidazole antifungal agent. Miconazole (Monistat) is common made into miconazole nitrate (riconazole; Prilagin; R 14889; Vodol; Zeasorb AF; Zimycan). 
 

						</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/Miconazole-Monistat.html</link>
            <guid isPermaLink="false">BF4DE677-F0E2-4327-8C44-A4B47547A298</guid>
            <pubDate>Fri, 15 Apr 2011 15:34:14 +0800</pubDate>
        </item>
        <item>
            <title>Econazole nitrate (Spectazole) &gt;99%(HPLC) | (CAS 24169-02-6) | Order Online | Ecostatin; Epi-Pevaryl; Gyno-Pevaryl; Gynoryl; Ifenec; Micogin; NSC 243115; Palavale; Pevaryl, Econazole nitrate (Spectazole)</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Econazole%20nitrate.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/Econazole-nitrate-Spectazole.html" style="color:#062074">Econazole nitrate</a>  (Cat No. S2535)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/researcharea.html" style="color:#062074">By Research Area</a> » <a href="http://www.selleckchem.com/research_Infection.html" style="color:#062074">Infection</a>  » <a href="http://www.selleckchem.com/products/Econazole-nitrate-Spectazole.html"style="color:#062074">Econazole nitrate-Spectazole</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Econazole nitrate (Spectazole) is an imidazole class antifungal medication. 
 

						</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/Econazole-nitrate-Spectazole.html</link>
            <guid isPermaLink="false">6CB59CE5-2A32-4B3F-85B3-3BF218A0374E</guid>
            <pubDate>Fri, 15 Apr 2011 15:29:36 +0800</pubDate>
        </item>
        <item>
            <title>Maprotiline hydrochloride &gt;99%(HPLC) | (CAS 10347-81-6) | Reuptake inhibitor Inhibitor | Deprilept, Ludiomil, Psymion, Maprotiline hydrochloride</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Maprotiline%20hydrochloride.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/Maprotiline-hydrochloride.html" style="color:#062074">Maprotiline hydrochloride</a>  (Cat No. S2517)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Neuro-Signaling.html" style="color:#062074">Neuro Signaling</a> » <a href="http://www.selleckchem.com/pathways_Reuptake-inhibitor.html"style="color:#062074">Reuptake inhibitor</a> » <a href="http://www.selleckchem.com/products/Maprotiline-hydrochloride.html"style="color:#062074">Maprotiline hydrochloride</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Maprotiline hydrochloride (Deprilept, Ludiomil, Psymion) is a selective noradrenalin re-uptake inhibitor and a tetracyclic antidepressant.
 

						</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/Maprotiline-hydrochloride.html</link>
            <guid isPermaLink="false">29E2768A-B382-4DE2-9BFC-F3D909347A6B</guid>
            <pubDate>Fri, 8 Apr 2011 14:06:55 +0800</pubDate>
        </item>
        <item>
            <title>Naphazoline hydrochloride (Naphcon) (Synonyms Naphcon, Albalon)</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Naphazoline%20hydrochloride.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/Naphazoline-hydrochloride-Naphcon.html" style="color:#062074">Naphazoline hydrochloride-Naphcon </a>  (Cat No. S2519)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/researcharea.html" style="color:#062074">By Research Area</a> » <a href="http://www.selleckchem.com/research_Cardiovascular-Disease.html" style="color:#062074">Cardiovascular Disease</a> » <a href="http://www.selleckchem.com/products/Naphazoline-hydrochloride-Naphcon.html">Naphazoline hydrochloride-Naphcon</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Naphazoline hydrochloride (Naphcon) is an ocular vasoconstrictor and imidazoline derivative sympathomimetic amine.
 

						</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/Naphazoline-hydrochloride-Naphcon.html</link>
            <guid isPermaLink="false">D51FCBB7-C21B-46ED-89A3-FC0AEAFC94A6</guid>
            <pubDate>Fri, 8 Apr 2011 14:02:08 +0800</pubDate>
        </item>
        <item>
            <title>Epinephrine bitartrate (Adrenalinium) (Synonyms D02149, Adrenalinetartrate, Adrenaline tatrate, Epinephrine Acid Tartrate)</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Epinephrine%20bitartrate.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href=http://www.selleckchem.com/products/Epinephrine-bitartrate-Adrenalinium.html" style="color:#062074">Epinephrine bitartrate-Adrenalinium
</a>  (Cat No. S2521)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_GPCR.html" style="color:#062074">GPCR</a> » <a href="http://www.selleckchem.com/pathways_adrenergic-receptor.html"style="color:#062074">adrenergic receptor
</a>» <a href="http://www.selleckchem.com/products/Epinephrine-bitartrate-Adrenalinium.html"style="color:#062074">Epinephrine bitartrate-Adrenalinium
</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Epinephrine bitartrate (D02149, Adrenalinium) is alpha- and beta-adrenergic receptor stimulator.
 

						</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/Epinephrine-bitartrate-Adrenalinium.html</link>
            <guid isPermaLink="false">10724333-6EF2-4334-B091-08D7824A6707</guid>
            <pubDate>Fri, 8 Apr 2011 13:21:12 +0800</pubDate>
        </item>
        <item>
            <title>L-Adrenaline (Epinephrine) (Synonyms Adrenaline, d-Adrenaline, Adnephrine, Adrenalin, Chelafrin, Epinefrina, Epinephran, Epirenan, Exadri)</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/L-Adrenaline.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/L-Adrenaline-Epinephrine.html" style="color:#062074">L-Adrenaline (Epinephrine)</a>  (Cat No. S2522)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/researcharea.html" style="color:#062074">By Research Area</a> » <a href="http://www.selleckchem.com/research_Metabolic-Disease.html" style="color:#062074">Metabolic Disease</a> » <a href="http://www.selleckchem.com/products/L-Adrenaline-Epinephrine.html"style="color:#062074">L-Adrenaline-Epinephrine
</a></div>
							<strong style="color:#062074">Biological Activity:</strong>L-Adrenaline (Epinephrine) belongs to a group of the compounds known as catecholamines.
 

						</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/L-Adrenaline-Epinephrine.html</link>
            <guid isPermaLink="false">4381D7D5-B4FE-4EFE-AB22-14497DBD893C</guid>
            <pubDate>Fri, 8 Apr 2011 13:16:06 +0800</pubDate>
        </item>
        <item>
            <title>Phenytoin sodium (Dilantin) (Synonyms Aleviatin; Diphenylhydantoin sodium; Eptoin; Phenytoin soluble; Prompt; Phenytek)</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Phenytoin%20sodium.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/Phenytoin-sodium-Dilantin.html" style="color:#062074">Phenytoin sodium (Dilantin)</a>  (Cat No. S2524)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/researcharea.html" style="color:#062074">By Research Area</a> » <a href="http://www.selleckchem.com/research_Neurological-Disease.html" style="color:#062074">Neurological Disease</a> » <a href="http://www.selleckchem.com/products/Phenytoin-sodium-Dilantin.html">Phenytoin sodium-Dilantin
</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Phenytoin sodium (Dilantin) is an inactive voltage-gated sodium channel stabilizer.
 

						</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/Phenytoin-sodium-Dilantin.html</link>
            <guid isPermaLink="false">48DECDE4-2581-433B-8FA4-0CB2B16712AA</guid>
            <pubDate>Fri, 8 Apr 2011 13:12:56 +0800</pubDate>
        </item>
        <item>
            <title>Phenytoin (Lepitoin) (Synonyms Di-Hydan; Dihycon; Dilabid; Diphedan; Diphenat; Diphenylan; Diphenylhydantoin; Hydantol; Lehydan; NS)</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Phenytoin.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/Phenytoin-Lepitoin.html" style="color:#062074">Phenytoin (Lepitoin)</a>  (Cat No. S2525)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/researcharea.html" style="color:#062074">By Research Area</a> » <a href="http://www.selleckchem.com/research_Neurological-Disease.html" style="color:#062074">Neurological Disease</a> » <a href="http://www.selleckchem.com/products/Phenytoin-Lepitoin.html">Phenytoin-Lepitoin
</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Phenytoin (Lepitoin; NSC 8722; Phenytek; Phenytoine; Sodanton; Zentropi) is an inactive voltage-gated sodium channel stabilizer.
 

						</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/Phenytoin-Lepitoin.html</link>
            <guid isPermaLink="false">63BDA4BC-ADE8-41C1-A787-301BA48E3B42</guid>
            <pubDate>Fri, 8 Apr 2011 13:06:17 +0800</pubDate>
        </item>
        <item>
            <title>UK 383367 &gt;99%(HPLC) | (CAS 348622-88-8 ) | Procollagen C-proteinase Inhibitor | UK-383367, UK 383367</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/UK%20383367.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/UK-383367.html" style="color:#062074">UK 383367</a>  (Cat No. S2224)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Proteases_HSP90_HSP70.html" style="color:#062074">Proteases/HSP90/HSP70</a> » <a href="http://www.selleckchem.com/pathways_Procollagen-C-proteinase.html" style="color:#062074">Procollagen C-proteinase</a>» <a href="http://www.selleckchem.com/products/UK-383367.html" style="color:#062074">UK 383367</a></div>
							<strong style="color:#062074">Biological Activity:</strong>UK 383367 is a novel, potent procollagen C-proteinase (PCP) inhibitor with an IC50 of 44 nM. 
 

						</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/UK-383367.html</link>
            <guid isPermaLink="false">3BAD7651-BD3B-4E0D-B631-9E4F397C6829</guid>
            <pubDate>Wed, 6 Apr 2011 13:16:25 +0800</pubDate>
        </item>
        <item>
            <title>MCOPPB trihydrochloride &gt;99%(HPLC) | (CAS 1028969-49-4) | Opioid recepotor Inhibitor | MCOPPB trihydrochloride</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/MCOPPB%20trihydrochloride.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/MCOPPB-trihydrochloride.html" style="color:#062074">MCOPPB trihydrochloride</a>  (Cat No. S2223)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_GPCR.html" style="color:#062074">GPCR</a> » <a href="http://www.selleckchem.com/pathways_Opioid-recepotor.html" style="color:#062074">Opioid recepotor</a>» <a href="http://www.selleckchem.com/products/MCOPPB-trihydrochloride.html" style="color:#062074">MCOPPB</a></div>
							<strong style="color:#062074">Biological Activity:</strong>MCOPPB trihydrochloride is a trihydrochloride form of MCOPPB that is a new nonpeptide nociceptin/orphanin FQ peptide (NOP)-receptor agonist with a pKi of 10.07 ± 0.01 for the human NOP receptor.
						</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/MCOPPB-trihydrochloride.html</link>
            <guid isPermaLink="false">8FD1A136-20E0-474D-9C6B-2F4D8AB59B62</guid>
            <pubDate>Wed, 6 Apr 2011 11:20:53 +0800</pubDate>
        </item>
        <item>
            <title>PF 3716556 &gt;99%(HPLC) | (CAS 928774-43-0) | proton pump Inhibitor | PF-3716556, PF-03716556, PF 3716556</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/PF%203716556.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/PF-3716556.html" style="color:#062074">PF 3716556</a>  (Cat No. S2222)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Others.html" style="color:#062074">others</a> » <a href="http://www.selleckchem.com/pathways_proton-pump.html" style="color:#062074">proton pump</a>» <a href="http://www.selleckchem.com/products/PF-3716556.html" style="color:#062074">PF 3716556</a></div>
							<strong style="color:#062074">Biological Activity:</strong>PF-03716556 is a potent, and selective acid pump antagonist with pIC50 of 6.026 ± 0.112, 6.038 ± 0.039 and 6.009 ± 0.209 at pH 6.4 for the inhibition of H+, K+-ATPase activity of porcine, canine and human ion-leaky membrane vesicles, respectively.
						</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/PF-3716556.html</link>
            <guid isPermaLink="false">BD9F93A4-238F-47F0-97F7-C56C0986E9A9</guid>
            <pubDate>Wed, 6 Apr 2011 11:08:58 +0800</pubDate>
        </item>
        <item>
            <title>Curcumol &gt;99%(HPLC) | (CAS 4871-97-0) | Order Online | Curcumol</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Curcumol.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/Curcumol.html" style="color:#062074">Curcumol</a>  (Cat No. S2407)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/researcharea.html" style="color:#062074">By Research Area</a> » <a href="http://www.selleckchem.com/research_Metabolic-Disease.html" style="color:#062074">Metabolic Disease</a> » <a href="http://www.selleckchem.com/products/Curcumol.html" style="color:#062074">Curcumol</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Curcumol is a common traditional Chinese medicine with antitumor activities. Curcumol is isolated from Rhizoma Curcumae. 
						</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/Curcumol.html</link>
            <guid isPermaLink="false">7AA84EAF-2881-46C6-9167-2403E5EDE0FE</guid>
            <pubDate>Thu, 24 Mar 2011 14:56:23 +0800</pubDate>
        </item>
        <item>
            <title>Chrysophanic acid (Chrysophanol) &gt;99%(HPLC) | (CAS 481-74-3) | EGFR(HER) Inhibitor | mTOR Inhibitor | Chrysophanol, NSC 37132, NSC 646567, Chrysophanic acid (Chrysophanol)</title>
            <description>
                <![CDATA[<table width="100%" border=0 cellpadding=1 bordercolorlight="#f0f0f0" bordercolordark="#a0a0a0" cellspacing=2>
<tr valign=top>
<td width=367 valign=middle><img alt="src="http://www.selleckchem.com/pic/digi/Chrysophanic%20acid.gif" style="margin-right:20px" " src="http://www.selleckchem.com/pic/digi/Chrysophanic%20acid.gif"></td>
<td valign=middle><b>Product:</b><a href="http://www.selleckchem.com/products/Chrysophanic-acid-Chrysophanol.html?ItemId=279178&utm_campaign=RSS&utm_source=RSS&utm_medium=RSS" style="color:#062074"> Chrysophanic acid</a> (Cat No. S2406)<br />
<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Angiogenesis_Tyrosine-Kinase.html" style="color:#062074">Angiogenesis/Tyrosine Kinase</a> » <a href="http://www.selleckchem.com/pathways_EGFR(HER).html" style="color:#062074">EGFR(HER)</a> / <a href="http://www.selleckchem.com/pathways_mTOR.html" style="color:#062074">mTOR </a> » <a href="http://www.selleckchem.com/products/Chrysophanic-acid-Chrysophanol.html" style="color:#062074">Chrysophanic acid-Chrysophanol
</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Chrysophanic acid (rhein, rheic acid, rhubarbarin; Chrysophanol) is a EGFR/mTOR pathway inhibitor. 
						</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/Chrysophanic-acid-Chrysophanol.html</link>
            <guid isPermaLink="false">A7C90811-81E0-4F84-93F0-BD89087BD156</guid>
            <pubDate>Thu, 24 Mar 2011 14:52:14 +0800</pubDate>
        </item>
        <item>
            <title>Sophocarpine &gt;99%(HPLC) | (CAS 6483-15-4) | Order Online | Sophocarpine</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Sophocarpine.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/Sophocarpine.html" style="color:#062074">Sophocarpinel</a>  (Cat No. S2405)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/researcharea.html" style="color:#062074">By Research Area</a> » <a href="http://www.selleckchem.com/research_Cardiovascular-Disease.html" style="color:#062074">Cardiovascular Disease</a> » <a href="http://www.selleckchem.com/products/Sophocarpine.html" style="color:#062074">Sophocarpine</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Sophocarpine is a human ether-à-go-go-related gene (HERG) inhibitor with an IC(50) of about 0.2 mM. 
						</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/Sophocarpine.html</link>
            <guid isPermaLink="false">039D1C43-39DE-4FDD-9223-EAC6E09D01B1</guid>
            <pubDate>Thu, 24 Mar 2011 14:44:20 +0800</pubDate>
        </item>
        <item>
            <title>Isoliquiritigenin &gt;99%(HPLC) | (CAS 961-29-5) | Order Online | Isoliquiritigenin</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Isoliquiritigenin.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/Isoliquiritigenin.html" style="color:#062074">Isoliquiritigenin</a>  (Cat No. S2404)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/researcharea.html" style="color:#062074">By Research Area</a> » <a href="http://www.selleckchem.com/research_chemotherapeutic-agent.html" style="color:#062074">chemotherapeutic agent </a> » <a href="http://www.selleckchem.com/products/Isoliquiritigenin.html" style="color:#062074">Isoliquiritigenin</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Isoliquiritigenin (GU 17) is a strong nod gene- and glyceollin resistance-inducing flavonoid from soybean root exudate.
						</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/Isoliquiritigenin.html</link>
            <guid isPermaLink="false">91B85E65-5ECD-4951-937C-D7B3812EFA9D</guid>
            <pubDate>Thu, 24 Mar 2011 14:40:38 +0800</pubDate>
        </item>
        <item>
            <title>Sodium Danshensu &gt;99%(HPLC) | (CAS 67920-52-9) | Order Online | Sodium Danshensu</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Sodium%20Danshensu.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/Sodium-Danshensu.html" style="color:#062074">Sodium Danshensu</a>  (Cat No. S2401)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/researcharea.html" style="color:#062074">By Research Area</a> » <a href="http://www.selleckchem.com/research_Neurological-Disease.html" style="color:#062074">Neurological Disease </a> » <a href="http://www.selleckchem.com/products/Sodium-Danshensu.html" style="color:#062074">Sodium Danshensu</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Sodium Danshensu is a mono sodium of danshensu which is a compound isolated from Salvia miltiorrhiza Bge.
						</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/Sodium-Danshensu.html</link>
            <guid isPermaLink="false">0CA4CA14-DDC0-4809-BF88-18E1D4AD7525</guid>
            <pubDate>Thu, 24 Mar 2011 14:21:08 +0800</pubDate>
        </item>
        <item>
            <title>Cyclovirobuxin D (Bebuxine) &gt;99%(HPLC) | (CAS 860-79-7) | Order Online | Bebuxine, Cyclovirobuxine, Cyclovirobuxine D, NSC 91722, Cyclovirobuxin D (Bebuxine)</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Cyclovirobuxin%20D.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/Cyclovirobuxin-D-Bebuxine.html" style="color:#062074">Cyclovirobuxin D</a>  (Cat No. S2402)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/researcharea.html" style="color:#062074">By Research Area</a> » <a href="http://www.selleckchem.com/research_Cardiovascular-Disease.html" style="color:#062074">Cardiovascular Disease </a> » <a href="http://www.selleckchem.com/products/Cyclovirobuxin-D-Bebuxine.html" style="color:#062074">Cyclovirobuxin D </a></div>
							<strong style="color:#062074">Biological Activity:</strong>Cyclovirobuxine D (bebuxine; Cyclovirobuxine) is an active compound extracted from Buxus microphylla, which has been used for treating acute myocardial ischemia.
						</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/Cyclovirobuxin-D-Bebuxine.html</link>
            <guid isPermaLink="false">0C2FC767-D8B3-4D9A-805D-2276F38440E4</guid>
            <pubDate>Thu, 24 Mar 2011 14:19:31 +0800</pubDate>
        </item>
        <item>
            <title>Sodium Danshensu &gt;99%(HPLC) | (CAS 67920-52-9) | Order Online | Sodium Danshensu</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Sodium%20Danshensu.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/Sodium-Danshensu.html" style="color:#062074">Sodium Danshensu</a>  (Cat No. S2401)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/researcharea.html" style="color:#062074">By Research Area</a> » <a href="http://www.selleckchem.com/research_Neurological-Disease.html" style="color:#062074">Neurological Disease </a> » <a href="http://www.selleckchem.com/products/Sodium-Danshensu.html" style="color:#062074">Sodium Danshensu
</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Sodium Danshensu is a mono sodium of danshensu which is a compound isolated from Salvia miltiorrhiza Bge.
						</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/Sodium-Danshensu.html</link>
            <guid isPermaLink="false">9BF0EACB-9C47-40C7-9D06-9FE8CB8503F0</guid>
            <pubDate>Thu, 24 Mar 2011 14:15:19 +0800</pubDate>
        </item>
        <item>
            <title>&gt;Rhein (Monorhein) &gt;99%(HPLC) | (CAS 478-43-3) | Order Online | Monorhein, NSC 38629, Rheic acid, Rheinic acid, Rhubarb yellow, Rhein (Monorhein)</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Rhein.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/Rhein-Monorhein.html" style="color:#062074">Rhein</a>  (Cat No. S2400)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/researcharea.html" style="color:#062074">By Research Area</a> » <a href="http://www.selleckchem.com/research_Immunology.html" style="color:#062074">Immunology </a> » <a href="http://www.selleckchem.com/products/Rhein-Monorhein.html" style="color:#062074">Rhein-Monorhein

</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Rhein(Monorhein; NSC 38629; Rheic acid; Rheinic acid) is a constituent of rhubarb which was isolated from the fresh rhizome of Rheum coreanum Nakai.
						</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/Rhein-Monorhein.html</link>
            <guid isPermaLink="false">0F360F28-5353-4AD3-8481-836E7A220883</guid>
            <pubDate>Thu, 24 Mar 2011 14:13:00 +0800</pubDate>
        </item>
        <item>
            <title>Dihydromyricetin (Ampeloptin) &gt;99%(HPLC) | (CAS 27200-12-0) | Order Online | Ampeloptin, Ampelopsin,(+)-Ampelopsin, (+)-Dihydromyricetin, Dihydromyricetin (Ampeloptin)</title>
            <description>
                <![CDATA[<table width="100%" border=0 cellpadding=1 bordercolorlight="#f0f0f0" bordercolordark="#a0a0a0" cellspacing=2>
<tr valign=top>
<td width=367 valign=middle><img alt="src="http://www.selleckchem.com/pic/digi/Dihydromyricetin.gif" style="margin-right:20px" " src="http://www.selleckchem.com/pic/digi/Dihydromyricetin.gif"><br />
</td>
<td valign=middle><b>Product:</b><a href="http://www.selleckchem.com/products/Dihydromyricetin-Ampeloptin.html" style="color:#062074"> Dihydromyricetin</a> (Cat No. S2399)<br />
<b>Category:</b><a href="http://www.selleckchem.com/researcharea.html" style="color:#062074"> By Research Area</a> » <a href="http://www.selleckchem.com/research_Metabolic-Disease.html" style="color:#062074">Metabolic Disease </a>» <a href="http://www.selleckchem.com/products/Dihydromyricetin-Ampeloptin.html" style="color:#062074">Dihydromyricetin-Ampeloptin </a><br />
<b>Biological Activity:</b>Dihydromyricetin (Ampelopsin (flavanol); Ampeloptin) is a natural antioxidant with good prospects. <br />
</td>
</tr>
</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/Dihydromyricetin-Ampeloptin.html</link>
            <guid isPermaLink="false">A36DB960-C2A9-4FD6-B623-CB20EDA3998F</guid>
            <pubDate>Thu, 24 Mar 2011 14:09:08 +0800</pubDate>
        </item>
        <item>
            <title>Coenzyme Q10 (CoQ10) &gt;99%(HPLC) | (CAS 303-98-0) | Order Online | Ubiquinone, Ubidecarenone, coenzyme Q, CoQ10, Coenzyme Q10 (CoQ10)</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Coenzyme%20Q10.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/Coenzyme-Q10-CoQ10.html" style="color:#062074">Coenzyme Q10</a>  (Cat No. S2398)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/researcharea.html" style="color:#062074">By Research Area</a> » <a href="http://www.selleckchem.com/research_Metabolic-Disease.html" style="color:#062074">Metabolic Disease </a> » <a href="http://www.selleckchem.com/products/Coenzyme-Q10-CoQ10.html" style="color:#062074">Coenzyme Q10-CoQ10


</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Coenzyme Q10 (ubiquinone, ubidecarenone, coenzyme Q) is a component of the electron transport chain and participates in aerobic cellular respiration.
						</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/Coenzyme-Q10-CoQ10.html</link>
            <guid isPermaLink="false">BA1793E3-C9F5-45EA-933D-61CB1A1261F8</guid>
            <pubDate>Thu, 24 Mar 2011 14:03:42 +0800</pubDate>
        </item>
        <item>
            <title>Irinotecan Hcl Trihydrate (Campto) &gt;99%(HPLC) | (CAS 136572-09-3) | Topoisomerase Inhibitor | CPT 11, Camptosar, Campto, Irinotecan, Irinotecan Hcl Trihydrate (Campto)</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/Irinotecan%20hydrochloride%20trihydrate.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/Irinotecan-Hcl-Trihydrate-Campto.html" style="color:#062074">Irinotecan Hcl Trihydrate</a>  (Cat No. S2217)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Cell-Cycle_Checkpoint.html" style="color:#062074">Cell Cycle/Checkpoint</a> » <a href="http://www.selleckchem.com/pathways_Topoisomerase.html" style="color:#062074">Topoisomerase</a>» <a href="http://www.selleckchem.com/products/Irinotecan-Hcl-Trihydrate-Campto.html" style="color:#062074">Irinotecan Hcl Trihydrate-Campto

</a>
</a></div>
							<strong style="color:#062074">Biological Activity:</strong>Irinotecan hydrochloride trihydrate is a hydrochloride trihydrate of irinotecan (Camptosar, Campto, CPT-11) which is a topoisomerase I inhibitor with IC50 of 15.8 and 5.17 μM for LoVo cells and HT-29 cells, respectively.
						</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/Irinotecan-Hcl-Trihydrate-Campto.html</link>
            <guid isPermaLink="false">B131B626-4C7D-4712-B650-A25513134C78</guid>
            <pubDate>Thu, 24 Mar 2011 13:58:35 +0800</pubDate>
        </item>
        <item>
            <title>DAPT (GSI-IX) &gt;99%(HPLC) | (CAS 208255-80-5) | Y-secretase Inhibitor | GSI-IX, DAPT (GSI-IX)</title>
            <description>
                <![CDATA[<table width ="100%" border="0">
<tr>
						<td width="367" style="border-right:1px solid #828CAA"><img src="http://www.selleckchem.com/pic/digi/DAPT.gif" style="margin-right:20px"></td>
						<td style="padding-left:20px; vertical-align:top">
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Product:</strong> <a href="http://www.selleckchem.com/products/DAPT-GSI-IX.html" style="color:#062074">DAPT</a>  (Cat No. S2215)</a></div>
							<div style="margin:0 0 5px 0"><strong style="color:#062074">Category:</strong> <a href="http://www.selleckchem.com/pharmacologicalact.html" style="color:#062074">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Neuro-Signaling.html" style="color:#062074">Neuro Signaling</a> » <a href="http://www.selleckchem.com/pathways_Y-secretase.html" style="color:#062074">Y-secretase</a> » <a href="http://www.selleckchem.com/products/DAPT-GSI-IX.html" style="color:#062074">DAPT-GSI-IX
 </a></div>
 </a></div>
							<strong style="color:#062074">Biological Activity:</strong>DAPT (GSI-IX) is a γ-secretase inhibitor with IC50 of 0.12 and 0.2 μM for total Aβ and Aβ42 levels, respectively.
						</td>
					</tr>
					</table>]]>
            </description>
            <link>http://www.selleckchem.com/products/DAPT-GSI-IX.html</link>
            <guid isPermaLink="false">18F3CED0-0D44-455F-BFD7-45BB37D000F2</guid>
            <pubDate>Thu, 24 Mar 2011 13:49:07 +0800</pubDate>
        </item>
        <item>
            <title>Tetrandrine (Fanchinine) &gt;99%(HPLC) | (CAS 518-34-3) | calcium channel Inhibitor | Fanchinine, Hanfangchin A, NSC 77037, S,S-(+)-Tetrandrine, Sinomenine A, TTD</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/pic/digi/Tetrandrine.gif"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/Tetrandrine.gif"></a><br />
<br />
Catalog No.: <a href="http://www.selleckchem.com/products/Tetrandrine-Fanchinine.html">S2403</a><br />
 Product:<a href="http://www.selleckchem.com/products/Tetrandrine-Fanchinine.html">Tetrandrine(Fanchinine)</a><br />
 Category:<a href="http://www.selleckchem.com/pharmacologicalact.html">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Ion-channel.html">Ion channel</a> » <a href="http://www.selleckchem.com/pathways_calcium-channel.html">calcium channel</a> » <a href="http://www.selleckchem.com/products/Tetrandrine-Fanchinine.html">Tetrandrine-Fanchinine</a><br />
 Biological Activity:Tetrandrine (Fanchinine; Hanfangchin A) is a calcium channel blocker with an IC50 of 38.23± 25.77 μM.]]>
            </description>
            <link>http://www.selleckchem.com/products/Tetrandrine-Fanchinine.html</link>
            <guid isPermaLink="false">2CE327DF-0239-43E8-AD6E-326E3270722D</guid>
            <pubDate>Wed, 23 Mar 2011 13:32:58 +0800</pubDate>
        </item>
        <item>
            <title>Cyclovirobuxin D (Bebuxine) &gt;99%(HPLC) | (CAS 860-79-7) | Order Online | Bebuxine, Cyclovirobuxine, Cyclovirobuxine D, NSC 91722, Cyclovirobuxin D (Bebuxine)</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/pic/digi/Cyclovirobuxin%20D.gif"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/Cyclovirobuxin%20D.gif"></a><br />
<br />
Catalog No.: <a href="http://www.selleckchem.com/products/Cyclovirobuxin-D-Bebuxine.html">S2402</a> <br />
Product:<a href="http://www.selleckchem.com/products/Cyclovirobuxin-D-Bebuxine.html">Cyclovirobuxin D(Bebuxine</a>) <br />
Category:<a href="http://www.selleckchem.com/researcharea.html">By Research Area</a> » <a href="http://www.selleckchem.com/research_Cardiovascular-Disease.html">Cardiovascular Disease</a> » <a href="http://www.selleckchem.com/products/Cyclovirobuxin-D-Bebuxine.html">Cyclovirobuxin D-Bebuxine</a> <br />
Biological Activity:Cyclovirobuxine D (bebuxine; Cyclovirobuxine) is an active compound extracted from Buxus microphylla, which has been used for treating acute myocardial ischemia.]]>
            </description>
            <link>http://www.selleckchem.com/products/Cyclovirobuxin-D-Bebuxine.html</link>
            <guid isPermaLink="false">3A6BA2B9-99CC-49F2-910F-F3B8D0BB29EF</guid>
            <pubDate>Wed, 23 Mar 2011 13:28:33 +0800</pubDate>
        </item>
        <item>
            <title>Sodium Danshensu &gt;99%(HPLC) | (CAS 67920-52-9) | Order Online | Sodium Danshensu</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/pic/digi/Sodium%20Danshensu.gif"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/Sodium%20Danshensu.gif"></a><br />
<br />
Catalog No.: <a href="http://www.selleckchem.com/products/Sodium-Danshensu.html">S2401</a><br />
Product:<a href="http://www.selleckchem.com/products/Sodium-Danshensu.html">Sodium Danshensu</a><br />
Category:<a href="http://www.selleckchem.com/researcharea.html">By Research Area</a> » <a href="http://www.selleckchem.com/research_Neurological-Disease.html">Neurological Disease</a> » <a href="http://www.selleckchem.com/products/Sodium-Danshensu.html">Sodium Danshensu</a><br />
Biological Activity:Sodium Danshensu is a mono sodium of danshensu which is a compound isolated from Salvia miltiorrhiza Bge.]]>
            </description>
            <link>http://www.selleckchem.com/products/Sodium-Danshensu.html</link>
            <guid isPermaLink="false">30C9D159-C640-4C3D-8C7E-B49FBC1DC23A</guid>
            <pubDate>Wed, 23 Mar 2011 13:16:59 +0800</pubDate>
        </item>
        <item>
            <title>Rhein (Monorhein) &gt;99%(HPLC) | (CAS 478-43-3) | Order Online | Monorhein, NSC 38629, Rheic acid, Rheinic acid, Rhubarb yellow, Rhein (Monorhein)</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/pic/digi/Rhein.gif"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/Rhein.gif"></a><br />
<br />
Catalog No.: <a href="http://www.selleckchem.com/products/Rhein-Monorhein.html">S2400</a><br />
Product:<a href="http://www.selleckchem.com/products/Rhein-Monorhein.html">Rhein(Monorhein)</a><br />
Category:<a href="http://www.selleckchem.com/researcharea.html">By Research Area</a> » <a href="http://www.selleckchem.com/research_Immunology.html">Immunology</a> » <a href="http://www.selleckchem.com/products/Rhein-Monorhein.html">Rhein-Monorhein</a><br />
Biological Activity:Rhein(Monorhein; NSC 38629; Rheic acid; Rheinic acid) is a constituent of rhubarb which was isolated from the fresh rhizome of Rheum coreanum Nakai.]]>
            </description>
            <link>http://www.selleckchem.com/products/Rhein-Monorhein.html</link>
            <guid isPermaLink="false">CEE25D10-7763-491B-A065-D34DFEEEC158</guid>
            <pubDate>Wed, 23 Mar 2011 11:15:37 +0800</pubDate>
        </item>
        <item>
            <title>Dihydromyricetin (Ampeloptin) &gt;99%(HPLC) | (CAS 27200-12-0) | Order Online | Ampeloptin, Ampelopsin,(+)-Ampelopsin, (+)-Dihydromyricetin, Dihydromyricetin (Ampeloptin)</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/pic/digi/Dihydromyricetin.gif"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/Dihydromyricetin.gif"></a><br />
<br />
Catalog No.: <a href="http://www.selleckchem.com/products/Dihydromyricetin-Ampeloptin.html">S2398</a> <br />
Product:<a href="http://www.selleckchem.com/products/Dihydromyricetin-Ampeloptin.html">Coenzyme Q10(CoQ10)</a><br />
Category:<a href="http://www.selleckchem.com/researcharea.html">By Research Area</a> » <a href="http://www.selleckchem.com/research_Metabolic-Disease.html">Metabolic Disease</a> » <a href="http://www.selleckchem.com/products/Dihydromyricetin-Ampeloptin.html">Coenzyme Q10-CoQ10</a> <br />
Biological Activity:Coenzyme Q10 (ubiquinone, ubidecarenone, coenzyme Q) is a component of the electron transport chain and participates in aerobic cellular respiration, generating energy in the form of ATP.]]>
            </description>
            <link>http://www.selleckchem.com/products/Dihydromyricetin-Ampeloptin.html</link>
            <guid isPermaLink="false">939B1CCC-D4F2-4DE7-801B-89A7F7EBE1F4</guid>
            <pubDate>Wed, 23 Mar 2011 11:08:08 +0800</pubDate>
        </item>
        <item>
            <title>Coenzyme Q10 (CoQ10) &gt;99%(HPLC) | (CAS 303-98-0) | Order Online | Ubiquinone, Ubidecarenone, coenzyme Q, CoQ10, Coenzyme Q10 (CoQ10)</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/pic/digi/Coenzyme%20Q10.gif"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/Coenzyme%20Q10.gif"></a><br />
<br />
Catalog No.: <a href="http://www.selleckchem.com/products/Coenzyme-Q10-CoQ10.html">S2398</a><br />
Product:<a href="http://www.selleckchem.com/products/Coenzyme-Q10-CoQ10.html">Coenzyme Q10(CoQ10)</a><br />
Category: <a href="http://www.selleckchem.com/researcharea.html">By Research Area</a> » <a href="http://www.selleckchem.com/research_Metabolic-Disease.html">Metabolic Disease</a> » <a href="http://www.selleckchem.com/products/Coenzyme-Q10-CoQ10.html">Coenzyme Q10-CoQ10</a><br />
 Biological Activity:Coenzyme Q10 (ubiquinone, ubidecarenone, coenzyme Q) is a component of the electron transport chain and participates in aerobic cellular respiration, generating energy in the form of ATP.]]>
            </description>
            <link>http://www.selleckchem.com/products/Coenzyme-Q10-CoQ10.html</link>
            <guid isPermaLink="false">88914A82-BA6A-4315-8B08-78BABDC08950</guid>
            <pubDate>Wed, 23 Mar 2011 10:58:15 +0800</pubDate>
        </item>
        <item>
            <title>Candesartan cilexetil (Atacand) &gt;99%(HPLC) | (CAS 145040-37-5) | Angiotensin receptor Inhibitor | Atacand, Amias, Blopress, Ratacand, TCV 116, TCY 116, Candesartan cilexetil (Atacand)</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/pic/digi/ATACAND%20(candesartan%20cilexetil).gif"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/ATACAND%20(candesartan%20cilexetil).gif"></a><br />
Catalog No.: <a href="http://www.selleckchem.com/products/Candesartan-cilexetil-Atacand.html">S2037</a> <br />
Product:<a href="http://www.selleckchem.com/products/Candesartan-cilexetil-Atacand.html">Candesartan cilexetil(Atacand)</a> <br />
Category: <a href="http://www.selleckchem.com/pharmacologicalact.html" target="_blank">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_GPCR.html">GPCR</a> » <a href="http://www.selleckchem.com/pathways_Angiotensin-receptor.html">Angiotensin receptor</a> » <a href="http://www.selleckchem.com/products/Candesartan-cilexetil-Atacand.html">Candesartan cilexetil-Atacand</a><br />
Biological Activity:Candesartan cilexetil (TCV 116, TCY 116) is a specific nonpeptide Ang II receptor (ATR) antagonist and the prodrug of candesartan which is an ATR antagonist with an IC50 of 15 µg/kg. .]]>
            </description>
            <link>http://www.selleckchem.com/products/Candesartan-cilexetil-Atacand.html</link>
            <category domain="">inhibitor</category>
            <guid isPermaLink="false">81D4065C-3E08-4BDE-AD2A-A68C345CB03A</guid>
            <pubDate>Wed, 23 Mar 2011 10:40:05 +0800</pubDate>
        </item>
        <item>
            <title>U 95666E (Sumanirole maleate) &gt;99%(HPLC) | (CAS 179386-44-8 ) | Order Online | Sumanirole maleate, PNU 95666, U95666E, U 95666E (Sumanirole maleate)</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/pic/digi/Sumanirole%20maleate.gif"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/Sumanirole%20maleate.gif"></a><br />
Catalog No.: <a href="http://www.selleckchem.com/products/U-95666E%28Sumanirole-maleate%29.html">S2191</a><br />
Product:<a href="http://www.selleckchem.com/products/U-95666E%28Sumanirole-maleate%29.html">U 95666E(Sumanirole maleate)</a><br />
Category:<a href="http://www.selleckchem.com/researcharea.html">By Research Area</a> » <a href="http://www.selleckchem.com/research_Neurological-Disease.html">Neurological Disease</a> » <a href="http://www.selleckchem.com/products/U-95666E%28Sumanirole-maleate%29.html">U 95666E(Sumanirole maleate)</a><br />
 Biological Activity:U 95666E is a highly selective D2 receptor full agonist with an ED50 of about 46 nM.]]>
            </description>
            <link>http://www.selleckchem.com/products/U-95666E%28Sumanirole-maleate%29.html</link>
            <guid isPermaLink="false">EAAFCE1E-F7F9-4039-82C9-8EB8C66BD9F1</guid>
            <pubDate>Mon, 21 Mar 2011 16:45:41 +0800</pubDate>
        </item>
        <item>
            <title>Pyroxamide (NSC 696085) &gt;99%(HPLC) | (CAS 382180-17-8 ) | HDAC Inhibitor | NSC 696085, NSC-696085, Pyroxamide (NSC 696085)</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/pic/digi/Pyroxamide.gif"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/Pyroxamide.gif"></a><br />
Catalog No.: <a href="http://www.selleckchem.com/products/Pyroxamide%28NSC-696085%29.html">S2190</a><br />
Product: <a href="http://www.selleckchem.com/products/Pyroxamide%28NSC-696085%29.html">Pyroxamide(NSC 696085)</a><br />
 Category:<a href="http://www.selleckchem.com/pharmacologicalact.html">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_HDAC.html">HDAC</a> » <a href="http://www.selleckchem.com/pathways_HDAC.html">HDAC</a> » <a href="http://www.selleckchem.com/products/Pyroxamide%28NSC-696085%29.html">Pyroxamide(NSC 696085)</a>. <br />
Biological Activity:Pyroxamide(NSC 696085) is a potent histone deacetylase inhibitor with an IC50 of 100 nM for HDAC-1.]]>
            </description>
            <link>http://www.selleckchem.com/products/Pyroxamide%28NSC-696085%29.html</link>
            <guid isPermaLink="false">EF54C188-C06C-4204-BBD5-9659016850AB</guid>
            <pubDate>Mon, 21 Mar 2011 16:43:23 +0800</pubDate>
        </item>
        <item>
            <title>Phenprocoumon (Marcumar) &gt;99%(HPLC) | (CAS 435-97-2 ) | Order Online | Marcoumar, Marcumar and Falithrom, Phenprocoumon (Marcumar)</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/pic/digi/Phenprocoumon.gif"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/Phenprocoumon.gif"></a><br />
Catalog No.: <a href="http://www.selleckchem.com/products/Phenprocoumon%28Marcumar%29.html">S2188</a><br />
Product:<a href="http://www.selleckchem.com/products/Phenprocoumon%28Marcumar%29.html">Phenprocoumon(Marcumar)</a><br />
 Category:<a href="http://www.selleckchem.com/researcharea.html">By Research Area</a> » <a href="http://www.selleckchem.com/research_Cardiovascular-Disease.html">Cardiovascular Disease</a> » <a href="http://www.selleckchem.com/products/Phenprocoumon%28Marcumar%29.html">Phenprocoumon(Marcumar)</a><br />
Biological Activity: Phenprocoumon(Marcumar) is a vitamin K reductase with an IC50 of 1 µM.]]>
            </description>
            <link>http://www.selleckchem.com/products/Phenprocoumon%28Marcumar%29.html</link>
            <guid isPermaLink="false">829018D1-0ACE-465E-A696-16E82904E307</guid>
            <pubDate>Mon, 21 Mar 2011 16:36:48 +0800</pubDate>
        </item>
        <item>
            <title>GSK461364 &gt;99%(HPLC) | (CAS 929095-18-1) | PLK Inhibitor | GSK 461364, GSK461364</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/pic/digi/GSK%20461364.gif"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/GSK%20461364.gif"></a><br />
Catalog No.: <a href="http://www.selleckchem.com/products/GSK461364.html">S2193</a><br />
 Product:<a href="http://www.selleckchem.com/products/GSK461364.html">GSK461364</a><br />
Category:<a href="http://www.selleckchem.com/pharmacologicalact.html">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Cell-Cycle_Checkpoint.html">Cell Cycle/Checkpoint</a> » <a href="http://www.selleckchem.com/pathways_PLK.html">PLK</a> » <a href="http://www.selleckchem.com/products/GSK461364.html">GSK461364</a><br />
Biological Activity:GSK 461364 is a potent small molecule Polo-like kinase 1 (PLK1) inhibitor with a Ki of 2.2 nM.]]>
            </description>
            <link>http://www.selleckchem.com/products/GSK461364.html</link>
            <guid isPermaLink="false">EFEC85B2-7D9D-478F-870D-68F9A709F0AA</guid>
            <pubDate>Mon, 21 Mar 2011 16:34:15 +0800</pubDate>
        </item>
        <item>
            <title>Phenprocoumon (Marcumar) &gt;99%(HPLC) | (CAS 435-97-2 ) | Order Online | Marcoumar, Marcumar and Falithrom, Phenprocoumon (Marcumar)</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/pic/digi/Phenprocoumon.gif"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/Phenprocoumon.gif"></a><br />
Catalog No.: <a href="http://www.selleckchem.com/products/Phenprocoumon%28Marcumar%29.html">S2188</a><br />
Product:<a href="http://www.selleckchem.com/products/Phenprocoumon%28Marcumar%29.html">Phenprocoumon(Marcumar)</a><br />
 Category:<a href="http://www.selleckchem.com/researcharea.html">By Research Area</a> » <a href="http://www.selleckchem.com/research_Cardiovascular-Disease.html">Cardiovascular Disease</a> » <a href="http://www.selleckchem.com/products/Phenprocoumon%28Marcumar%29.html">Phenprocoumon(Marcumar)</a><br />
Biological Activity:Phenprocoumon(Marcumar) is a vitamin K reductase with an IC50 of 1 µM.]]>
            </description>
            <link>http://www.selleckchem.com/products/Phenprocoumon%28Marcumar%29.html</link>
            <guid isPermaLink="false">8B824E84-87AE-4A76-8743-CC0E14704D04</guid>
            <pubDate>Mon, 21 Mar 2011 16:27:57 +0800</pubDate>
        </item>
        <item>
            <title>GSK461364 &gt;99%(HPLC) | (CAS 929095-18-1) | PLK Inhibitor | GSK 461364, GSK461364</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/pic/digi/GSK%20461364.gif"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/GSK%20461364.gif"></a><br />
Catalog No.:<a href="http://www.selleckchem.com/products/GSK461364.html">S2193</a><br />
Product: <a href="http://www.selleckchem.com/products/GSK461364.html">GSK461364</a><br />
 Category:<a href="http://www.selleckchem.com/pharmacologicalact.html">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Cell-Cycle_Checkpoint.html">Cell Cycle/Checkpoint</a> » <a href="http://www.selleckchem.com/pathways_PLK.html">PLK</a> » <a href="http://www.selleckchem.com/products/GSK461364.html">GSK461364</a><br />
Biological Activity:GSK 461364 is a potent small molecule Polo-like kinase 1 (PLK1) inhibitor with a Ki of 2.2 nM.]]>
            </description>
            <link>http://www.selleckchem.com/products/GSK461364.html</link>
            <guid isPermaLink="false">B6BCB31C-B63E-4726-9FEC-B799E4F58DCB</guid>
            <pubDate>Mon, 21 Mar 2011 16:24:30 +0800</pubDate>
        </item>
        <item>
            <title>Avasimibe (CI-1011) &gt;99%(HPLC) | (CAS 166518-60-1 ) | Order Online | Avasimibe (CI-1011)</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/pic/digi/Avasimibe.gif"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/Avasimibe.gif"></a><br />
Catalog No.: <a href="http://www.selleckchem.com/products/Avasimibe%28CI-1011%29.html">S2187</a><br />
Product: <a href="http://www.selleckchem.com/products/Avasimibe%28CI-1011%29.html">Avasimibe(CI-1011)</a><br />
 Category:<a href="http://www.selleckchem.com/researcharea.html">By Research Area</a> » <a href="http://www.selleckchem.com/research_Metabolic-Disease.html">Metabolic Disease</a> » <a href="http://www.selleckchem.com/products/Avasimibe%28CI-1011%29.html">Avasimibe(CI-1011)</a><br />
Biological Activity: Avasimibe(CI-1011) is a novel orally bioavailable acyl coenzyme A:cholesterol acyltransferase inhibitor with IC50 of 2.9, 13.9, 26.5 µM for CYP2C9, CYP1A2, and CYP2C19.]]>
            </description>
            <link>http://www.selleckchem.com/products/Avasimibe%28CI-1011%29.html</link>
            <guid isPermaLink="false">D74EB8FF-1C54-42CF-A220-97AFA5568697</guid>
            <pubDate>Mon, 21 Mar 2011 16:14:16 +0800</pubDate>
        </item>
        <item>
            <title>Acitazanolast &gt;99%(HPLC) | (CAS 114607-46-4 ) | Order Online | WP-871, Acitazanolast</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/pic/digi/Acitazanolast.gif"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/Acitazanolast.gif"></a><br />
Catalog No.: <a href="http://www.selleckchem.com/products/Acitazanolast.html">S2189</a> <br />
Product: <a href="http://www.selleckchem.com/products/Acitazanolast.html">Acitazanolast</a> <br />
Category: <a href="http://www.selleckchem.com/researcharea.html">By Research Area</a> » <a href="http://www.selleckchem.com/research_Immunology.html">Immunology</a>» <a href="http://www.selleckchem.com/products/Acitazanolast.html">Acitazanolast</a><br />
 Biological Activity:Acitazanolast is an active metabolite of tazanolast and anti-allergic drug. In a study, pretreatment with topical instillation of acitazanolast hydrate inhibited the dye leakage significantly.]]>
            </description>
            <link>http://www.selleckchem.com/products/Acitazanolast.html</link>
            <guid isPermaLink="false">36F607FE-5774-4E3D-82EB-2B9E194425BA</guid>
            <pubDate>Mon, 21 Mar 2011 16:07:45 +0800</pubDate>
        </item>
        <item>
            <title>Vinflunine Tartrate &gt;99%(HPLC) | (CAS 1201898-17-0 ) | Microtubule Inhibitor | Vinflunine Tartrate</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/pic/digi/Vinflunine%20Tartrate.gif"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/Vinflunine%20Tartrate.gif"></a><br />
Catalog No.: <a href="http://www.selleckchem.com/products/Vinflunine-Tartrate.html">S2209</a><br />
 Product:<a href="http://www.selleckchem.com/products/Vinflunine-Tartrate.html">Vinflunine Tartrate</a><br />
Category<a href="http://www.selleckchem.com/pharmacologicalact.html">:By Product Pathways</a> »<a href="http://www.selleckchem.com/pharmacological_Cell-Cycle_Checkpoint.html">Cell Cycle/Checkpoint</a> » <a href="http://www.selleckchem.com/pathways_Microtubule.html">Microtubule</a>» <a href="http://www.selleckchem.com/products/Vinflunine-Tartrate.html">Vinflunine Tartrate</a> <br />
Biological Activity: Vinflunine Tartrate is a tartrate salt of vinflunine that is a new microtubule inhibitor with IC50 of 18.8 nM.]]>
            </description>
            <link>http://www.selleckchem.com/products/Vinflunine-Tartrate.html</link>
            <guid isPermaLink="false">9F9B8671-FBE3-463D-AEA4-856761BEC532</guid>
            <pubDate>Mon, 21 Mar 2011 15:59:02 +0800</pubDate>
        </item>
        <item>
            <title>R788 (Fostamatinib disodium) &gt;99%(HPLC) | (CAS 1025687-58-4) | Syk Inhibitor | FosD, tamatinib fosdium, R788 (Fostamatinib disodium)</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/pic/digi/R%20788.gif"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/R%20788.gif"></a><br />
Catalog No.: <a href="http://www.selleckchem.com/products/R788%28Fostamatinib-disodium%29.html">S2206</a> <br />
Product:<a href="http://www.selleckchem.com/products/R788%28Fostamatinib-disodium%29.html">R788(Fostamatinib disodium)</a><br />
Category:<a href="http://www.selleckchem.com/pharmacologicalact.html">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Angiogenesis_Tyrosine-Kinase.html">Angiogenesis/Tyrosine Kinase</a> » <a href="http://www.selleckchem.com/pathways_Syk.html">Syk</a>» <a href="http://www.selleckchem.com/products/R788%28Fostamatinib-disodium%29.html">R788(Fostamatinib disodium)</a><br />
Biological Activity:R788(FosD) is a selective Syk inhibitor with an IC50 of 41 nM.]]>
            </description>
            <link>http://www.selleckchem.com/products/R788%28Fostamatinib-disodium%29.html</link>
            <guid isPermaLink="false">BF3EE128-1550-4079-AF12-C59527B8C716</guid>
            <pubDate>Mon, 21 Mar 2011 15:55:18 +0800</pubDate>
        </item>
        <item>
            <title>Formestane &gt;99%(HPLC) | (CAS 566-48-3) | Aromatase Inhibitor | Lentaron(R), 17-dione, CGP-32349, NSC 282175, Formestane</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/pic/digi/Formestane.gif"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/Formestane.gif"></a><br />
Catalog No.: <a href="http://www.selleckchem.com/products/Formestane.html">S2208</a><br />
Product: <a href="http://www.selleckchem.com/products/Formestane.html">Formestane</a><br />
Category: <a href="http://www.selleckchem.com/pharmacologicalact.html">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Hormone.html">Hormone</a> » <a href="http://www.selleckchem.com/pathways_Aromatase.html">Aromatase</a> » <a href="http://www.selleckchem.com/products/Formestane.html">Formestane</a><br />
Biological Activity: Formestane(Lentaron(R)) is a second generation selective aromatase inhibitor with an IC50 of 80 nM..]]>
            </description>
            <link>http://www.selleckchem.com/products/Formestane.html</link>
            <guid isPermaLink="false">7A2481F9-8F41-49CE-A159-B51C52E6828E</guid>
            <pubDate>Mon, 21 Mar 2011 13:41:17 +0800</pubDate>
        </item>
        <item>
            <title>Atazanavir sulfate &gt;99%(HPLC) | (CAS 229975-97-7) | HSP-90 Inhibitor | BMS-232632-05, CGP-73547, Reyataz, Zrivada, Atazanavir sulfate</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/pic/digi/Atazanavir%20Sulfate.gif"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/Atazanavir%20Sulfate.gif"></a><br />
Catalog No.: <a href="http://www.selleckchem.com/products/Atazanavir-sulfate%28Reyataz%29.html">S2204</a><br />
Product: <a href="http://www.selleckchem.com/products/Atazanavir-sulfate%28Reyataz%29.html">Atazanavir sulfate</a> <br />
Category:<a href="http://www.selleckchem.com/pharmacologicalact.html">By Product Pathways</a> »<a href="http://www.selleckchem.com/pharmacological_Proteases_HSP90_HSP70.html">Proteases/HSP90/HSP70</a> » <a href="http://www.selleckchem.com/pathways_HSP-90.html">HSP-90</a> » <a href="http://www.selleckchem.com/products/Atazanavir-sulfate%28Reyataz%29.html">Atazanavir sulfate(Reyataz)</a><br />
 Biological Activity:Atazanavir sulfate(BMS-232632-05) is a sulfate salt form of atazanavir (BMS-232632) that is an highly potent HIV protease inhibitor with an EC50 and EC90 of 2.6~5.3 nM and 9~15 nM in cell culture.]]>
            </description>
            <link>http://www.selleckchem.com/products/Atazanavir-sulfate%28Reyataz%29.html</link>
            <guid isPermaLink="false">F4F80CB2-9F7A-40B8-B02B-F13B31F8E9ED</guid>
            <pubDate>Mon, 21 Mar 2011 13:37:41 +0800</pubDate>
        </item>
        <item>
            <title>OSI-420 (Desmethyl Erlotinib,CP-473420) &gt;99%(HPLC) | (CAS 183320-51-6) | EGFR(HER) Inhibitor | Desmethyl Erlotinib,CP-473420, OSI-420 (Desmethyl Erlotinib,CP-473420)</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/pic/digi/OSI%20420.gif"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/OSI%20420.gif"></a><br />
Catalog No.: <a href="http://www.selleckchem.com/products/OSI-420-Desmethyl-Erlotinib,CP-473420.html">S2205</a><br />
 Product:<a href="http://www.selleckchem.com/products/OSI-420-Desmethyl-Erlotinib,CP-473420.html">OSI-420(Desmethyl Erlotinib,CP-473420)</a><br />
 Category:<a href="http://www.selleckchem.com/pharmacologicalact.html">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Angiogenesis_Tyrosine-Kinase.html">Angiogenesis/Tyrosine Kinase</a>» <a href="http://www.selleckchem.com/pathways_EGFR%28HER%29.html">EGFR(HER)</a> » <a href="http://www.selleckchem.com/products/OSI-420-Desmethyl-Erlotinib,CP-473420.html">OSI-420-Desmethyl-Erlotinib,CP-473420</a><br />
Biological Activity: OSI 420 is an active metabolite of erlotinib which is an orally active EGFR tyrosin kinase inhibitor with IC50 of 2 and 20 nM for the inhibition of human EGFR and EGFR autophosphorylation in tumor cells.]]>
            </description>
            <link>http://www.selleckchem.com/products/OSI-420-Desmethyl-Erlotinib,CP-473420.html</link>
            <guid isPermaLink="false">3564B26C-75BB-4660-AB05-814C0292451E</guid>
            <pubDate>Mon, 21 Mar 2011 13:35:24 +0800</pubDate>
        </item>
        <item>
            <title>NVP-BHG712 &gt;99%(HPLC) | (CAS 940310-85-0) | Src-bcr-Abl Inhibitor | VEGFR-PDGFR Inhibitor | NVP-BHG712</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/pic/digi/NVP-BHG712.gif"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/NVP-BHG712.gif"></a><br />
Catalog No.: <a href="http://www.selleckchem.com/products/NVP-BHG712.html">S2202</a><br />
Product: <a href="http://www.selleckchem.com/products/NVP-BHG712.html">NVP-BHG712</a><br />
Category:<a href="http://www.selleckchem.com/pharmacologicalact.html">By Product Pathways</a> » » <a href="http://www.selleckchem.com/pathways_Src-bcr-Abl.html">Src-bcr-Abl</a> <a href="http://www.selleckchem.com/pathways_VEGFR-PDGFR.html">/ VEGFR-PDGFR</a> » <a href="http://www.selleckchem.com/products/NVP-BHG712.html">NVP-BHG712</a><br />
Biological Activity: NVP-BHG712 is a small molecule specific EphB4, VEGFR2, c-raf, c-src and c-Abl kinase inhibitor with ED50 of 25 nM, 4.2, 0.4, 1.3 and 1.7μM, respectively.]]>
            </description>
            <link>http://www.selleckchem.com/products/NVP-BHG712.html</link>
            <guid isPermaLink="false">DBD56FA0-3681-4EAD-9E4B-D1108A8318E6</guid>
            <pubDate>Mon, 21 Mar 2011 13:33:14 +0800</pubDate>
        </item>
        <item>
            <title>Mubritinib (TAK 165) &gt;99%(HPLC) | (CAS 366017-09-6) | EGFR(HER) Inhibitor | TAK 165, TAK165, Mubritinib (TAK 165)</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/pic/digi/Mubritinib.gif"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/Mubritinib.gif"></a><br />
Catalog No.: <a href="http://www.selleckchem.com/products/Mubritinib-TAK-165.html">S2216</a><br />
Product: <a href="http://www.selleckchem.com/products/Mubritinib-TAK-165.html">Mubritinib(TAK 165)</a> <br />
Category:<a href="http://www.selleckchem.com/pharmacologicalact.html">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Angiogenesis_Tyrosine-Kinase.html">Angiogenesis/Tyrosine Kinase</a> » <a href="http://www.selleckchem.com/pathways_EGFR%28HER%29.html">EGFR(HER)</a> » <a href="http://www.selleckchem.com/products/Mubritinib-TAK-165.html">Mubritinib-TAK-165</a><br />
Biological Activity: Roscovitine (TAK 165) is a potent EGFR and p34cdc2 inhibitor with IC50 of 6 nM and 0.2 µM, respectively.]]>
            </description>
            <link>http://www.selleckchem.com/products/Mubritinib-TAK-165.html</link>
            <guid isPermaLink="false">F2EC9A82-7015-4C17-8A72-F7C155018F1C</guid>
            <pubDate>Mon, 21 Mar 2011 13:30:05 +0800</pubDate>
        </item>
        <item>
            <title>AZ 960 &gt;99%(HPLC) | (CAS 905586-69-8) | JAK Inhibitor | AZ960, AZ 960</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/pic/digi/AZ%20960.gif"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/AZ%20960.gif"></a><br />
Catalog No.: <a href="http://www.selleckchem.com/products/AZ-960.html">S2214</a><br />
Product:<a href="http://www.selleckchem.com/products/AZ-960.html">AZ 960</a><br />
Category:<a href="http://www.selleckchem.com/pharmacologicalact.html">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Jak_Stat.html">Jak/Stat</a> » <a href="http://www.selleckchem.com/pathways_JAK.html">JAK</a> » <a href="http://www.selleckchem.com/products/AZ-960.html">AZ 960</a><br />
 Biological Activity: AZ 960 is a novel small molecule JAK2 kinase inhibitor with an IC50 and Ki of 3 mM and 0.45 nM in vitro, respectively.]]>
            </description>
            <link>http://www.selleckchem.com/products/AZ-960.html</link>
            <guid isPermaLink="false">F7C630F6-BDAB-4D4C-90A3-C68737E7CDFB</guid>
            <pubDate>Mon, 21 Mar 2011 13:15:34 +0800</pubDate>
        </item>
        <item>
            <title>Aliskiren hemifumarate &gt;99%(HPLC) | (CAS 173334-58-2) | Ras Inhibitor | Aliskiren hemifumarate</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/pic/digi/Aliskiren%20hemifumarate.gif"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/Aliskiren%20hemifumarate.gif"></a><br />
Catalog No.: <a href="http://www.selleckchem.com/products/Aliskiren-hemifumarate.html">S2199</a><br />
Product:<a href="http://www.selleckchem.com/products/Aliskiren-hemifumarate.html">Aliskiren hemifumarate</a><br />
Category:<a href="http://www.selleckchem.com/researcharea.html">By Research Area</a> » <a href="http://www.selleckchem.com/researcharea.html">Cardiovascular Disease</a> » <a href="http://www.selleckchem.com/products/Aliskiren-hemifumarate.html">Aliskiren hemifumarate</a><br />
Biological Activity:Aliskiren hemifumarate is a hemifumarate salt form of Aliskiren.Aliskiren is a direct renin inhibitor with an IC50 of 0.72 nM against renin.]]>
            </description>
            <link>http://www.selleckchem.com/products/Aliskiren-hemifumarate.html</link>
            <guid isPermaLink="false">59F01D11-73D4-48BA-8517-FAFB8FAF9D7C</guid>
            <pubDate>Sun, 13 Feb 2011 17:48:56 +0800</pubDate>
        </item>
        <item>
            <title>GSK461364 &gt;99%(HPLC) | (CAS 929095-18-1) | PLK Inhibitor | GSK 461364, GSK461364</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/pic/digi/GSK%20461364.gif"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/GSK%20461364.gif"></a><br />
Catalog No.: <a href="http://www.selleckchem.com/products/GSK461364.html">S2193</a><br />
Product:<a href="http://www.selleckchem.com/products/GSK461364.html">GSK461364</a><br />
Category:<a href="http://www.selleckchem.com/pharmacologicalact.html">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Cell-Cycle_Checkpoint.html">Cell Cycle/Checkpoint</a> »<a href="http://www.selleckchem.com/pathways_PLK.html">PLK</a> » <a href="http://www.selleckchem.com/products/GSK461364.html">GSK461364</a><br />
 Biological Activity:GSK 461364 is a potent small molecule Polo-like kinase 1 (PLK1) inhibitor with a Ki of 2.2 nM.]]>
            </description>
            <link>http://www.selleckchem.com/products/GSK461364.html</link>
            <guid isPermaLink="false">3922100A-217D-4E71-B710-167308B332AF</guid>
            <pubDate>Sun, 13 Feb 2011 17:45:07 +0800</pubDate>
        </item>
        <item>
            <title>A-966492 &gt;99%(HPLC) | (CAS 934162-61-5) | PARP Inhibitor | A966492, A-966492</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/pic/digi/A-966492.gif"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/A-966492.gif"></a><br />
Catalog No.: <a href="http://www.selleckchem.com/products/A-966492.html">S2197</a><br />
Product: <a href="http://www.selleckchem.com/products/A-966492.html">A-966492</a><br />
Category:<a href="http://www.selleckchem.com/pharmacologicalact.html">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_PARP.html">PARP</a> » <a href="http://www.selleckchem.com/pathways_PARP.html">PARP</a> » <a href="http://www.selleckchem.com/products/A-966492.html">A-966492</a><br />
Biological Activity:A-966492 is a highly potent and efficacious poly(ADP-ribose) polymerase (PARP) inhibitor with a Ki and EC50 of 1 nM.]]>
            </description>
            <link>http://www.selleckchem.com/products/A-966492.html</link>
            <guid isPermaLink="false">7089B913-9082-45AF-852D-DAFBE92BF944</guid>
            <pubDate>Sun, 13 Feb 2011 17:41:14 +0800</pubDate>
        </item>
        <item>
            <title>BIBR 953 (Dabigatran, Pradaxa) &gt;99%(HPLC) | (CAS 211914-51-1) | Order Online | Dabigatran, Pradaxa, BIBR953, BIBR 953 (Dabigatran, Pradaxa)</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/pic/digi/BIBR%20953.gif"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/BIBR%20953.gif"></a><br />
Catalog No.: <a href="http://www.selleckchem.com/products/BIBR-953%28Dabigatran%29.html">S2196</a><br />
Product:<a href="http://www.selleckchem.com/products/BIBR-953%28Dabigatran%29.html">BIBR 953</a><br />
Category:<a href="http://www.selleckchem.com/researcharea.html">By Research Area</a> » <a href="http://www.selleckchem.com/research_Cardiovascular-Disease.html">Cardiovascular Disease</a> » <a href="http://www.selleckchem.com/products/BIBR-953%28Dabigatran%29.html">BIBR 953(Dabigatran)</a><br />
Biological Activity:BIBR 953(Dabigatran) is a reversible, competitive, direct thrombin inhibitor.]]>
            </description>
            <link>http://www.selleckchem.com/products/BIBR-953%28Dabigatran%29.html</link>
            <guid isPermaLink="false">7FE62888-E500-4E2F-9EC7-9ECCED454F42</guid>
            <pubDate>Sun, 13 Feb 2011 17:37:23 +0800</pubDate>
        </item>
        <item>
            <title>R406 &gt;99%(HPLC) | (CAS 841290-81-1) | Syk Inhibitor | R406</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/pic/digi/R406.gif"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/R406.gif"></a><br />
Catalog No.: <a href="http://www.selleckchem.com/products/R406.html">S2194</a><br />
Product:<a href="http://www.selleckchem.com/products/R406.html">R406</a><br />
Category: <a href="http://www.selleckchem.com/pharmacologicalact.html">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Angiogenesis_Tyrosine-Kinase.html">Angiogenesis/Tyrosine Kinase</a> » <a href="http://www.selleckchem.com/pathways_Syk.html">Syk</a> » <a href="http://www.selleckchem.com/products/R406.html">R406</a><br />
 Biological Activity:R406 is an orally available spleen tyrosine kinase inhibitor with an IC50 of 41 nM.]]>
            </description>
            <link>http://www.selleckchem.com/products/R406.html</link>
            <guid isPermaLink="false">C18DF6C6-C5A8-4198-BCD2-7C28A8231DA7</guid>
            <pubDate>Sun, 13 Feb 2011 17:34:08 +0800</pubDate>
        </item>
        <item>
            <title>AZD8931 &gt;99%(HPLC) | (CAS 848942-61-0) | EGFR(HER) Inhibitor | AZD 8931, AZD8931</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/pic/digi/AZD8931.gif"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/AZD8931.gif"></a><br />
Catalog No.: <a href="http://www.selleckchem.com/products/AZD8931.html">S2192</a><br />
Product:<a href="http://www.selleckchem.com/products/AZD8931.html">AZD8931</a><br />
Category: <a href="http://www.selleckchem.com/pic/digi/AZD8931.gif">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Angiogenesis_Tyrosine-Kinase.html">Angiogenesis/Tyrosine Kinase</a>» <a href="http://www.selleckchem.com/pathways_EGFR%28HER%29.html">EGFR(HER)</a> » <a href="http://www.selleckchem.com/products/AZD8931.html">AZD8931</a><br />
 Biological Activity:AZD8931 is a novel potent reversible small molecule epidermal growth factor receptor, ERBB2 (HER2) and ERBB3 inhibitor with an IC50 of 4, 3, 4 nM, respectively.]]>
            </description>
            <link>http://www.selleckchem.com/products/AZD8931.html</link>
            <guid isPermaLink="false">92D2E0A7-AA58-4AD9-9D04-31255BBE5B66</guid>
            <pubDate>Sun, 13 Feb 2011 17:28:56 +0800</pubDate>
        </item>
        <item>
            <title>Acitazanolast &gt;99%(HPLC) | (CAS 114607-46-4 ) | Order Online | WP-871, Acitazanolast</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/pic/digi/Acitazanolast.gif"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/Acitazanolast.gif"></a><br />
Catalog No.: <a href="http://www.selleckchem.com/products/Acitazanolast.html">S2189</a><br />
Product:<a href="http://www.selleckchem.com/products/Acitazanolast.html">Acitazanolast</a><br />
Category: <a href="http://www.selleckchem.com/researcharea.html">By Research Area</a>» <a href="http://www.selleckchem.com/research_Immunology.html">Immunology</a> » <a href="http://www.selleckchem.com/products/Acitazanolast.html">Acitazanolast</a><br />
 Biological Activity: Acitazanolast is an active metabolite of tazanolast and anti-allergic drug.]]>
            </description>
            <link>http://www.selleckchem.com/products/Acitazanolast.html</link>
            <guid isPermaLink="false">8BECB649-E8AB-4C91-9934-D109160346E0</guid>
            <pubDate>Sun, 13 Feb 2011 17:23:50 +0800</pubDate>
        </item>
        <item>
            <title>Phenprocoumon (Marcumar) &gt;99%(HPLC) | (CAS 435-97-2 ) | Order Online | Marcoumar, Marcumar and Falithrom, Phenprocoumon (Marcumar)</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/pic/digi/Phenprocoumon.gif"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/Phenprocoumon.gif"></a><br />
Catalog No.: <a href="http://www.selleckchem.com/products/Phenprocoumon%28Marcumar%29.html">S2188</a><br />
Product: <a href="http://www.selleckchem.com/products/Phenprocoumon%28Marcumar%29.html">Phenprocoumon</a><br />
 Category: <a href="http://www.selleckchem.com/researcharea.html">By Research Area</a> » <a href="http://www.selleckchem.com/research_Cardiovascular-Disease.html">Cardiovascular Disease</a> » <a href="http://www.selleckchem.com/products/Phenprocoumon%28Marcumar%29.html">Phenprocoumon(Marcumar)</a><br />
Biological Activity: Phenprocoumon(Marcumar) is a vitamin K reductase with an IC50 of 1 µM.]]>
            </description>
            <link>http://www.selleckchem.com/products/Phenprocoumon%28Marcumar%29.html</link>
            <guid isPermaLink="false">3CB41684-A2D5-41C3-8D97-68B5ACFB2AB9</guid>
            <pubDate>Sun, 13 Feb 2011 14:15:56 +0800</pubDate>
        </item>
        <item>
            <title>Pyroxamide (NSC 696085) &gt;99%(HPLC) | (CAS 382180-17-8 ) | HDAC Inhibitor | NSC 696085, NSC-696085, Pyroxamide (NSC 696085)</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/pic/digi/Pyroxamide.gif"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/Pyroxamide.gif"></a><br />
Catalog No.: <a href="http://www.selleckchem.com/products/Pyroxamide%28NSC-696085%29.html">S2190</a><br />
Product: <a href="http://www.selleckchem.com/products/Pyroxamide%28NSC-696085%29.html">Pyroxamide</a><br />
 Category: <a href="http://www.selleckchem.com/pharmacologicalact.html">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_HDAC.html">HDAC</a> »<a href="http://www.selleckchem.com/pathways_HDAC.html">HDAC</a> » <a href="http://www.selleckchem.com/products/Pyroxamide%28NSC-696085%29.html">Pyroxamide(NSC 696085)</a><br />
Biological Activity: Pyroxamide(NSC 696085) is a potent histone deacetylase inhibitor with an IC50 of 100 nM for HDAC-1.]]>
            </description>
            <link>http://www.selleckchem.com/products/Pyroxamide%28NSC-696085%29.html</link>
            <guid isPermaLink="false">A6BB28A5-1D3C-4F1F-B470-DF2C934E0E19</guid>
            <pubDate>Sun, 13 Feb 2011 14:11:14 +0800</pubDate>
        </item>
        <item>
            <title>U 95666E (Sumanirole maleate) &gt;99%(HPLC) | (CAS 179386-44-8 ) | Order Online | Sumanirole maleate, PNU 95666, U95666E, U 95666E (Sumanirole maleate)</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/pic/digi/Sumanirole%20maleate.gif"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/Sumanirole%20maleate.gif"></a><br />
Catalog No.: <a href="http://www.selleckchem.com/products/U-95666E%28Sumanirole-maleate%29.html">S2191</a><br />
Product: <a href="http://www.selleckchem.com/products/U-95666E%28Sumanirole-maleate%29.html">U 95666E</a><br />
 Category:<a href="http://www.selleckchem.com/researcharea.html">By Research Area</a> » <a href="http://www.selleckchem.com/research_Neurological-Disease.html">Neurological Disease</a> » <a href="http://www.selleckchem.com/products/U-95666E%28Sumanirole-maleate%29.html">U 95666E(Sumanirole maleate</a>) <br />
Biological Activity:U 95666E(Sumanirole maleate) is a highly selective D2 receptor full agonist with an ED50 of about 46 nM.]]>
            </description>
            <link>http://www.selleckchem.com/products/U-95666E%28Sumanirole-maleate%29.html</link>
            <guid isPermaLink="false">100745BF-01C1-4B23-A632-4433A4CE536E</guid>
            <pubDate>Sun, 13 Feb 2011 14:06:13 +0800</pubDate>
        </item>
        <item>
            <title>Avasimibe (CI-1011) &gt;99%(HPLC) | (CAS 166518-60-1 ) | Order Online | Avasimibe (CI-1011)</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/pic/digi/Avasimibe.gif"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/Avasimibe.gif"></a><br />
Catalog No.: <a href="http://www.selleckchem.com/products/Avasimibe%28CI-1011%29.html">S2187</a> <br />
Product: <a href="http://www.selleckchem.com/products/Avasimibe%28CI-1011%29.html">Avasimibe</a><br />
Category: <a href="http://www.selleckchem.com/researcharea.html">By Research Area</a> » <a href="http://www.selleckchem.com/research_Cardiovascular-Disease.html">Cardiovascular Disease</a>» <a href="http://www.selleckchem.com/products/Avasimibe%28CI-1011%29.html">Avasimibe(CI-1011)</a><br />
 Biological Activity: Avasimibe(CI-1011) is a novel orally bioavailable acyl coenzyme A:cholesterol acyltransferase inhibitor with IC50 of 2.9, 13.9, 26.5 µM for CYP2C9, CYP1A2, and CYP2C19.]]>
            </description>
            <link>http://www.selleckchem.com/products/Avasimibe%28CI-1011%29.html</link>
            <guid isPermaLink="false">FE4A5A6F-3223-4AC7-BFF2-724572AE4BD9</guid>
            <pubDate>Sun, 13 Feb 2011 13:57:21 +0800</pubDate>
        </item>
        <item>
            <title>AG14361 &gt;99%(HPLC) | (CAS 328543-09-5) | PARP Inhibitor | AG 14361, AG14361</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/pic/digi/AG14361.gif"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/AG14361.gif"></a><br />
Catalog No.:<a href="http://www.selleckchem.com/products/AG14361.html">S2178</a><br />
Product<a href="http://www.selleckchem.com/products/AG14361.html">:AG14361</a><br />
Category:<a href="http://www.selleckchem.com/pharmacologicalact.html">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_PARP.html">PARP</a>» <a href="http://www.selleckchem.com/pathways_PARP.html">PARP</a> » <a href="http://www.selleckchem.com/products/AG14361.html">AG14361</a><br />
Biological Activity:AG14361 is a potent poly(ADP-ribose) polymerase (PARP-1) inhibitor with a GI50 of 10.9 µM.]]>
            </description>
            <link>http://www.selleckchem.com/products/AG14361.html</link>
            <guid isPermaLink="false">52CFE479-384A-441B-B91E-DC0204C5434D</guid>
            <pubDate>Sun, 16 Jan 2011 13:25:06 +0800</pubDate>
        </item>
        <item>
            <title>MLN9708 &gt;99%(HPLC) | (CAS 1201902-80-8) | Proteasome Inhibitor | MLN 9708, MLN9708</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/pic/digi/MLN9708.gif"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/MLN9708.gif"></a><br />
Catalog No.:<a href="http://www.selleckchem.com/products/MLN9708.html">S2181</a><br />
Product:<a href="http://www.selleckchem.com/products/MLN9708.html">MLN9708</a><br />
Category:<a href="http://www.selleckchem.com/pharmacologicalact.html">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Proteases_HSP90_HSP70.html">Proteases/HSP90/HSP70</a> » <a href="http://www.selleckchem.com/pathways_Proteasome.html">Proteasome</a>» <a href="http://www.selleckchem.com/products/MLN9708.html">MLN9708</a><br />
Biological Activity:MLN9708 is an orally bioavailable second generation proteasome inhibitor with potential antineoplastic activity.]]>
            </description>
            <link>http://www.selleckchem.com/products/MLN9708.html</link>
            <guid isPermaLink="false">F0C3A774-D963-4926-AD75-64CC54F3765D</guid>
            <pubDate>Sun, 16 Jan 2011 13:18:56 +0800</pubDate>
        </item>
        <item>
            <title>LY2784544 &gt;99%(HPLC) | (CAS 1229236-86-5) | JAK Inhibitor | LY 2784544, LY2784544</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/pic/digi/LY2784544.gif"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/LY2784544.gif"></a><br />
Catalog No.:<a href="http://www.selleckchem.com/products/LY2784544.html">S2179</a><br />
Product:<a href="http://www.selleckchem.com/products/LY2784544.html">LY2784544</a><br />
Category:<a href="http://www.selleckchem.com/pharmacologicalact.html">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Jak_Stat-Pathway.html">Jak/Stat Pathway</a> » <a href="http://www.selleckchem.com/pathways_JAK.html">JAK</a>» <a href="http://www.selleckchem.com/products/LY2784544.html">LY2784544</a><br />
Biological Activity:LY2784544 is a small molecule selective mutant JAK2 kinase inhibitor with an IC50 of 68 nM.]]>
            </description>
            <link>http://www.selleckchem.com/products/SB-743921.html</link>
            <guid isPermaLink="false">83E7D05D-4447-4D62-8022-892027779FED</guid>
            <pubDate>Sun, 16 Jan 2011 13:18:57 +0800</pubDate>
        </item>
        <item>
            <title>SB 743921 &gt;99%(HPLC) | (CAS 940929-33-9) | Ksp Inhibitor | SB743921, SB 743921</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/pic/digi/SB743921.gif"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/SB743921.gif"></a><br />
Catalog No.:<a href="http://www.selleckchem.com/products/SB-743921.html">S2182</a><br />
Product:<a href="http://www.selleckchem.com/products/SB-743921.html">SB 743921</a><br />
Category:<a href="http://www.selleckchem.com/pharmacologicalact.html">By Product Pathways</a>» <a href="http://www.selleckchem.com/pharmacological_Aurora_Ksp.html">Aurora/Ksp</a> »<a href="http://www.selleckchem.com/pathways_Ksp.html">Ksp</a> » <a href="http://www.selleckchem.com/products/SB-743921.html">SB 743921</a><br />
Biological Activity:SB743921 is a second generation, highly potent and active KSP inhibitor with a Ki of 0.1 nM for KSP (Eg5).]]>
            </description>
            <link>http://www.selleckchem.com/products/SB-743921.html</link>
            <guid isPermaLink="false">88FA225B-0751-4A30-9C62-BE88596B7599</guid>
            <pubDate>Sun, 16 Jan 2011 13:12:12 +0800</pubDate>
        </item>
        <item>
            <title>Domperidone (Motilium) &gt;99%(HPLC) | (CAS 57808-66-9) | Order Online | Motilium, Motillium, Motinorm, Costi, Domperidone (Motilium)</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/pic/digi/Domperidone.gif"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/Domperidone.gif"></a><br />
Catalog No.:<a href="http://www.selleckchem.com/products/Domperidone%28Motilium%29.html">S2461</a><br />
Product:<a href="http://www.selleckchem.com/products/Domperidone%28Motilium%29.html">Domperidone(Motilium)</a><br />
Category:<a href="http://www.selleckchem.com/researcharea.html">By Research Area</a>» <a href="http://www.selleckchem.com/research_Neurological-Disease.html">Neurological Disease</a> » <a href="http://www.selleckchem.com/products/Domperidone%28Motilium%29.html">Domperidone(Motilium)</a><br />
Biological Activity:Domperidone(Motilium) is a dopamine blocker and an antidopaminergic reagent. It blocks the action of.]]>
            </description>
            <link>http://www.selleckchem.com/products/Domperidone%28Motilium%29.html</link>
            <guid isPermaLink="false">EF0DEDCF-9E96-454B-822F-64E06160E659</guid>
            <pubDate>Sun, 16 Jan 2011 13:08:03 +0800</pubDate>
        </item>
        <item>
            <title>Dehydroepiandrosterone (DHEA) &gt;99%(HPLC) | (CAS 53-43-0) | Androgen Receptor Inhibitor | DHEA, Dehydroepiandrosterone (DHEA)</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/pic/digi/Dehydroepiandrosterone.gif"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/Dehydroepiandrosterone.gif"></a><br />
Catalog No.:<a href="http://www.selleckchem.com/products/Dehydroepiandrosterone%28DHEA%29.html">S2460</a><br />
Product:<a href="http://www.selleckchem.com/products/Dehydroepiandrosterone%28DHEA%29.html">Dehydroepiandrosterone</a><br />
Category:<a href="http://www.selleckchem.com/pharmacologicalact.html">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Others.html">Others</a> » <a href="http://www.selleckchem.com/pathways_Androgen-Receptor.html">Androgen Receptor</a> » <a href="http://www.selleckchem.com/products/Dehydroepiandrosterone%28DHEA%29.html">Dehydroepiandrosterone(DHEA)</a><br />
Biological Activity:Dehydroepiandrosterone(DHEA) is a 19-carbon endogenous natural steroid hormone.]]>
            </description>
            <link>http://www.selleckchem.com/products/Dehydroepiandrosterone%28DHEA%29.html</link>
            <guid isPermaLink="false">C9D27FB2-2AD5-4FC8-8E02-2EAF317C723B</guid>
            <pubDate>Sun, 16 Jan 2011 13:03:24 +0800</pubDate>
        </item>
        <item>
            <title>Clozapine (Clozaril) &gt;99%(HPLC) | (CAS 5786-21-0) | Order Online | Clozaril, Azaleptin, Leponex, Fazaclo, Froidir, Denzapine, Zaponex, Clozapine (Clozaril)</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/pic/digi/Chlorpromazine%20hydrochloride.gif"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/Chlorpromazine%20hydrochloride.gif"></a><br />
Catalog No.:<a href="http://www.selleckchem.com/products/Clozapine%28Clozaril%29.html">S2459</a><br />
Product:<a href="http://www.selleckchem.com/products/Clozapine%28Clozaril%29.html">Clozapine(Clozaril</a>)<br />
Category<a href="http://www.selleckchem.com/researcharea.html">:By Research Area</a>»<a href="http://www.selleckchem.com/researcharea.html">Neurological Disease</a> » <a href="http://www.selleckchem.com/products/Clozapine%28Clozaril%29.html">Clozapine(Clozaril)</a><br />
Biological Activity:Clozapine(Clozaril) is a potent 5-HT1C receptor antagonist with an IC50 of 110 nM for 5-HT-stimulated phosphoinositide hydrolysis.]]>
            </description>
            <link>http://www.selleckchem.com/products/Clozapine%28Clozaril%29.html</link>
            <guid isPermaLink="false">73233B8D-124D-466A-9EA4-03990AB3C998</guid>
            <pubDate>Sun, 16 Jan 2011 12:57:13 +0800</pubDate>
        </item>
        <item>
            <title>Chlorpromazine hydrochloride (Sonazine) &gt;99%(HPLC) | (CAS 69-09-0) | Order Online | Sonazine, Chloractil, Klorpromex, Promacid, Hebanil, Chlorpromazine hydrochloride (Sonazine)</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/pic/digi/Chlorpromazine%20hydrochloride.gif"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/Chlorpromazine%20hydrochloride.gif"></a><br />
Catalog No.:<a href="http://www.selleckchem.com/products/Chlorpromazine-hydrochloride%28Sonazine%29.html">S2456</a><br />
Product:<a href="http://www.selleckchem.com/products/Chlorpromazine-hydrochloride%28Sonazine%29.html">Chlorpromazine hydrochloride</a><br />
Category:<a href="http://www.selleckchem.com/researcharea.html">By Research Area</a> » <a href="http://www.selleckchem.com/research_Neurological-Disease.html">Neurological Disease</a> » <a href="http://www.selleckchem.com/products/Chlorpromazine-hydrochloride%28Sonazine%29.html">Chlorpromazine hydrochloride(Sonazine)</a><br />
Biological Activity:Chlorpromazine hydrochloride(Sonazine) is a dopamine and potassium channel inhibitor with IC50 of 6.1 and 16 µM for nward-rectifying K+ currents and time-independent outward currents.]]>
            </description>
            <link>http://www.selleckchem.com/products/Chlorpromazine-hydrochloride%28Sonazine%29.html</link>
            <guid isPermaLink="false">C63B0A73-AEAC-4F6F-84C0-A3AFB19AFE91</guid>
            <pubDate>Sun, 16 Jan 2011 12:53:49 +0800</pubDate>
        </item>
        <item>
            <title>Sotalol hydrochloride (Betapace) &gt;99%(HPLC) | (CAS 959-24-0) | Beta-1 receptor Inhibitor | Betapace, Betapace AF, Berlex Laboratories, Sotalex, Sotalol hydrochloride (Betapace)</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/pic/digi/Sotalol%20hydrochloride.gif"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/Sotalol%20hydrochloride.gif"></a><br />
Catalog No.:<a href="http://www.selleckchem.com/products/Sotalol-hydrochloride%28Betapace%29.html">S2509</a><br />
Product:<a href="http://www.selleckchem.com/products/Sotalol-hydrochloride%28Betapace%29.html">Sotalol hydrochloride</a><br />
Category:<a href="http://www.selleckchem.com/products/Sotalol-hydrochloride%28Betapace%29.html">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Ion-channel.html">Ion channel</a> »<a href="http://www.selleckchem.com/pathways_Beta-1-receptor.html">Beta-1 receptor</a> » <a href="http://www.selleckchem.com/products/Sotalol-hydrochloride%28Betapace%29.html">Sotalol hydrochloride(Betapace)</a><br />
Biological Activity:Sotalol(Betapace) is a non-selective beta blocker and a potassium channel blocker with an IC50 of 43 µM.]]>
            </description>
            <link>http://www.selleckchem.com/products/Sotalol-hydrochloride%28Betapace%29.html</link>
            <guid isPermaLink="false">F8DEB2A8-3506-4502-B459-B6D3D6DCCE44</guid>
            <pubDate>Sun, 16 Jan 2011 12:48:43 +0800</pubDate>
        </item>
        <item>
            <title>Scopolamine hydrobromide &gt;99%(HPLC) | (CAS 114-49-8) | Order Online | Scopolamine hydrobromide</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/pic/digi/Scopolamine%20hydrobromide.gif"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/Scopolamine%20hydrobromide.gif"></a><br />
Catalog No.:<a href="http://www.selleckchem.com/products/Scopolamine-hydrobromide.html">S2508</a><br />
Product:<a href="http://www.selleckchem.com/products/Scopolamine-hydrobromide.html">Scopolamine hydrobromide</a><br />
Category:<a href="http://www.selleckchem.com/researcharea.html">By Research Area</a> » <a href="http://www.selleckchem.com/research_Neurological-Disease.html">Neurological Disease</a> » <a href="http://www.selleckchem.com/products/Scopolamine-hydrobromide.html">Scopolamine hydrobromide</a><br />
Biological Activity:Scopolamine is a competitive muscarinic acetylcholine receptor with an IC50 of 55.3 ± 4.3 nM.]]>
            </description>
            <link>http://www.selleckchem.com/products/Scopolamine-hydrobromide.html</link>
            <guid isPermaLink="false">3C135EF1-71D4-42DC-9A7F-F04C3AE99543</guid>
            <pubDate>Sun, 16 Jan 2011 12:40:22 +0800</pubDate>
        </item>
        <item>
            <title>Salbutamol sulfate (Albuterol) &gt;99%(HPLC) | (CAS 51022-70-9) | Order Online | Albuterol, Ventolin, Aerolin, Ventorlin, Asthalin, Asthavent, Salbutamol sulfate (Albuterol)</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/pic/digi/Salbutamol%20sulfate.gif"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/Salbutamol%20sulfate.gif"></a><br />
Catalog No.:<a href="http://www.selleckchem.com/products/Salbutamol-sulfate%28Albuterol%29.html">S2507</a><br />
Product:<a href="http://www.selleckchem.com/products/Salbutamol-sulfate%28Albuterol%29.html">Salbutamol sulfate</a><br />
Category:<a href="http://www.selleckchem.com/researcharea.html">By Research Area</a> » <a href="http://www.selleckchem.com/research_Neurological-Disease.html">Neurological Disease</a> » <a href="http://www.selleckchem.com/products/Salbutamol-sulfate%28Albuterol%29.html">Salbutamol sulfate(Albuterol)</a><br />
Biological Activity:Salbutamol(Albuterol) is a short-acting β2-adrenergic receptor agonist with an IC50 of 8.93 µM.]]>
            </description>
            <link>http://www.selleckchem.com/products/Salbutamol-sulfate%28Albuterol%29.html</link>
            <guid isPermaLink="false">F243C64A-38AA-4265-B3E1-1A1BC5EB4520</guid>
            <pubDate>Sun, 16 Jan 2011 12:34:04 +0800</pubDate>
        </item>
        <item>
            <title>Rosiglitazone maleate &gt;99%(HPLC) | (CAS 155141-29-0) | Order Online | Rosiglitazone maleate</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/pic/digi/Rosiglitazone%20maleate.gif"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/Rosiglitazone%20maleate.gif"></a><br />
Catalog No.:<a href="http://www.selleckchem.com/products/Rosiglitazone-maleate.html">S2505</a><br />
Product:<a href="http://www.selleckchem.com/products/Rosiglitazone-maleate.html">Rosiglitazone maleate</a><br />
Category:<a href="http://www.selleckchem.com/researcharea.html">By Research Area</a>» <a href="http://www.selleckchem.com/research_Immunology.html">Immunology</a> » <a href="http://www.selleckchem.com/products/Rosiglitazone-maleate.html">Rosiglitazone maleate</a><br />
Biological Activity:Rosiglitazone maleate is an anti-diabetic drug in the thiazolidinedione class of drugs.]]>
            </description>
            <link>http://www.selleckchem.com/products/Rosiglitazone-maleate.html</link>
            <guid isPermaLink="false">22AD023E-A08A-48EF-89D1-68576E571CF4</guid>
            <pubDate>Sun, 16 Jan 2011 12:25:32 +0800</pubDate>
        </item>
        <item>
            <title>Racecadotril (Acetorphan) &gt;99%(HPLC) | (CAS 81110-73-8) | Order Online | Acetorphan, Racecadotril (Acetorphan)</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/pic/digi/Racecadotril.gif"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/Racecadotril.gif"></a><br />
Catalog No.:<a href="http://www.selleckchem.com/products/Racecadotril%28Acetorphan%29.html">S2503</a><br />
Product:<a href="http://www.selleckchem.com/products/Racecadotril%28Acetorphan%29.html">Racecadotril(Acetorphan</a>)<br />
Category:<a href="http://www.selleckchem.com/researcharea.html">By Research Area</a> » <a href="http://www.selleckchem.com/research_Metabolic-Disease.html">Metabolic Disease</a>» <a href="http://www.selleckchem.com/products/Racecadotril%28Acetorphan%29.html">Racecadotril(Acetorphan)</a><br />
Biological Activity:Racecadotril is a peripherally acting enkephalinase inhibitor with an IC50 of 4.5 µM.]]>
            </description>
            <link>http://www.selleckchem.com/products/Racecadotril%28Acetorphan%29.html</link>
            <guid isPermaLink="false">2FB277B9-2E40-49F6-993A-A33DD41731E5</guid>
            <pubDate>Sun, 16 Jan 2011 12:22:05 +0800</pubDate>
        </item>
        <item>
            <title>Hexestrol (Bibenzyl) &gt;99%(HPLC) | (CAS 84-16-2) | Estrogen receptor Inhibitor | Bibenzyl, Cycloestrol, Dihydro-stilbestro, Dihydrostilbestrol, Estra-Plex, Hexestrol (Bibenzyl)</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/pic/digi/Hexestrol.gif"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/Hexestrol.gif"></a><br />
Catalog No.:<a href="http://www.selleckchem.com/products/Hexestrol%28Bibenzyl%29.html">S2473</a><br />
Product:<a href="http://www.selleckchem.com/products/Hexestrol%28Bibenzyl%29.html">Hexestrol(Bibenzyl)</a><br />
Category:<a href="http://www.selleckchem.com/pharmacologicalact.html">By Product Pathways</a> »<a href="http://www.selleckchem.com/pharmacological_Hormone.html">Hormone</a>» <a href="http://www.selleckchem.com/pathways_Estrogen-receptor.html">Estrogen</a> receptor »<a href="http://www.selleckchem.com/products/Hexestrol%28Bibenzyl%29.html">Hexestrol(Bibenzyl)</a><br />
Biological Activity:Hexestrol(Bibenzyl) is a novel type of 17β-hydroxysteroid dehydrogenase, AKR1C1and AKR1C2 potent inhibitor with IC50 of 0.8, 9.5, 2.8 µM, respectively and exhibits strong affinity for estrogen receptors.]]>
            </description>
            <link>http://www.selleckchem.com/products/Hexestrol%28Bibenzyl%29.html</link>
            <guid isPermaLink="false">37FD42FC-97C2-412C-9A76-1A72A7C530F6</guid>
            <pubDate>Sun, 16 Jan 2011 12:18:32 +0800</pubDate>
        </item>
        <item>
            <title>Xylazine (Rompun) &gt;99%(HPLC) | (CAS 7361-61-7) | Order Online | Rompun, Xylazine (Rompun)</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/pic/digi/Xylazine.gif"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/Xylazine.gif"></a><br />
Catalog No.:<a href="http://www.selleckchem.com/products/Xylazine%28Rompun%29.html">S2516</a><br />
Product:<a href="http://www.selleckchem.com/products/Xylazine%28Rompun%29.html">Xylazine(Rompun)</a><br />
Category:<a href="http://www.selleckchem.com/researcharea.html">By Research Area</a>» <a href="http://www.selleckchem.com/research_Neurological-Disease.html">Neurological Disease » Xylazine(Rompun)</a><br />
Biological Activity:Xylazine(Rompun) is α2 class of adrenergic receptor agonist. As with other α2 agonists, adverse effects include bradycardia, conduction disturbances, and myocardial depression.]]>
            </description>
            <link>http://www.selleckchem.com/products/Xylazine%28Rompun%29.html</link>
            <guid isPermaLink="false">27E04CAE-F47D-4A47-B510-61C3600B4FE3</guid>
            <pubDate>Sun, 16 Jan 2011 12:12:52 +0800</pubDate>
        </item>
        <item>
            <title>Spectinomycin  hydrochloride &gt;99%(HPLC) | (CAS 21736-83-4) | Order Online | Spectinomycin  hydrochloride</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/pic/digi/Spectinomycin%20%20hydrochloride.gif"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/Spectinomycin%20%20hydrochloride.gif"></a><br />
Catalog No.:<a href="http://www.selleckchem.com/products/Spectinomycin--hydrochloride.html">S2510</a><br />
Product:<a href="http://www.selleckchem.com/products/Spectinomycin--hydrochloride.html">Spectinomycin hydrochloride</a><br />
Categoey:<a href="http://www.selleckchem.com/researcharea.html">By Research Area</a> » <a href="http://www.selleckchem.com/research_Infection.html">Infection</a> »<a href="http://www.selleckchem.com/products/Spectinomycin--hydrochloride.html">Spectinomycin hydrochloride</a><br />
Biological Activity:Spectinomycin hydrochloride is a new parenteral antibiotic prepared from Streptomyces spectabilis.]]>
            </description>
            <link>http://www.selleckchem.com/products/Spectinomycin--hydrochloride.html</link>
            <guid isPermaLink="false">9B38B12D-404F-466E-9363-D0EBA77C263C</guid>
            <pubDate>Sun, 16 Jan 2011 12:02:06 +0800</pubDate>
        </item>
        <item>
            <title>Emtricitabine (Emtriva) &gt;99%(HPLC) | (CAS 143491-57-0 ) | reverse transcriptase Inhibitor | Emtriva, Coviracil, Truvada, Atripla, Emtricitabine (Emtriva)</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/pic/digi/EMTRICITABINE%20%28emtricitabine%29.gif"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/EMTRICITABINE%20%28emtricitabine%29.gif"></a><br />
Catalog No.:<a href="http://www.selleckchem.com/products/Emtricitabine%28Emtriva%29.html">S2465</a><br />
Product:<a href="http://www.selleckchem.com/products/Emtricitabine%28Emtriva%29.html">Emtricitabine(Emtriva)</a><br />
Category:<a href="http://www.selleckchem.com/pharmacologicalact.html">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacologicalact.html">Others</a> »<a href="http://www.selleckchem.com/pharmacologicalact.html">NART</a> » <a href="http://www.selleckchem.com/products/Emtricitabine%28Emtriva%29.html">Emtricitabine(Emtriva</a>) <br />
Biological Activity:Emtricitabine(Emtriva) is a nucleoside reverse transcriptase inhibitor with an IC50 of 27.7 μM for HIV-1.]]>
            </description>
            <link>http://www.selleckchem.com/products/Emtricitabine%28Emtriva%29.html</link>
            <guid isPermaLink="false">C54B3851-23AF-4BF6-B0A2-E319B2B6B48E</guid>
            <pubDate>Sun, 16 Jan 2011 11:56:20 +0800</pubDate>
        </item>
        <item>
            <title>Manidipine dihydrochloride (CV-4093) &gt;99%(HPLC) | (CAS 89226-75-5) | Order Online | CV-4093, Manidipine dihydrochloride (CV-4093)</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/pic/digi/Manidipine%20dihydrochloride.gif"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/Manidipine%20dihydrochloride.gif"></a><br />
Catalog No.:<a href="http://www.selleckchem.com/products/Manidipine-dihydrochloride%28CV-4093%29.html">S2482</a><br />
Product: <a href="http://www.selleckchem.com/products/Manidipine-dihydrochloride%28CV-4093%29.html">Manidipine dihydrochloride</a><br />
Categoey:<a href="http://www.selleckchem.com/researcharea.html">By Research Area</a> »<a href="http://www.selleckchem.com/research_Cardiovascular-Disease.html">Cardiovascular Disease</a> » <a href="http://www.selleckchem.com/products/Manidipine-dihydrochloride%28CV-4093%29.html">Manidipine dihydrochloride(CV-4093)</a><br />
Biological Activity:Manidipine(CV-4093) is a lipophilic, third-generation, highly vasoselective dihydropyridine calcium antagonist with an IC50 of 2.6 nM.]]>
            </description>
            <link>http://www.selleckchem.com/products/Manidipine-dihydrochloride%28CV-4093%29.html</link>
            <guid isPermaLink="false">B237831A-BC31-4681-8462-7BDD302FD685</guid>
            <pubDate>Sun, 16 Jan 2011 11:51:56 +0800</pubDate>
        </item>
        <item>
            <title>Quinine hydrochloride dihydrate &gt;99%(HPLC) | (CAS 6119-47-7 ) | Order Online | Quinine hydrochloride dihydrate</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/pic/digi/Quinine%20hydrochloride%20dihydrate.gif"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/Quinine%20hydrochloride%20dihydrate.gif"></a><br />
Catalog No.:<a href="http://www.selleckchem.com/products/Quinine-hydrochloride-dihydrate.html">S2502</a><br />
Product:<a href="http://www.selleckchem.com/products/Quinine-hydrochloride-dihydrate.html">Quinine hydrochloride dihydrace</a><br />
Categoey:<a href="http://www.selleckchem.com/researcharea.html">By Research Area</a> » <a href="http://www.selleckchem.com/research_Neurological-Disease.html">Neurological Disease</a> » <a href="http://www.selleckchem.com/products/Quinine-hydrochloride-dihydrate.html">Quinine hydrochloride dihydrate</a><br />
Biological Activity: Quinine hydrochloride dihydrate is a natural white crystalline alkaloid having antipyretic (fever-reducing), antimalarial, analgesic (painkilling), anti-inflammatory properties and a bitter taste.]]>
            </description>
            <link>http://www.selleckchem.com/products/Quinine-hydrochloride-dihydrate.html</link>
            <guid isPermaLink="false">F92F18DC-C558-4228-911E-2033B7A21196</guid>
            <pubDate>Sun, 16 Jan 2011 11:17:07 +0800</pubDate>
        </item>
        <item>
            <title>Manidipine dihydrochloride (CV-4093) &gt;99%(HPLC) | (CAS 89226-75-5) | Order Online | CV-4093, Manidipine dihydrochloride (CV-4093)</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/products/AT7867.html"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/AT7867.gif"></a><br />
Catalog No.: <a href="http://www.selleckchem.com/products/AT7867.html">S1558</a><br />
Product: <a href="http://www.selleckchem.com/products/AT7867.html">AT7867</a><br />
Category: <a href="http://www.selleckchem.com/pharmacologicalact.html">By Product Pathways</a> »<a href="http://www.selleckchem.com/pharmacological_PI3K_Akt_mTOR.html">PI3K/Akt/mTOR</a> » <a href="http://www.selleckchem.com/pathways_Akt.html">Akt</a> » <a href="http://www.selleckchem.com/products/AT7867.html">AT7867</a><br />
Biological Activity: AT7867 is a potent and oral AKT and p70 S6 kinase inhibitor with an IC50 of 17 nM.]]>
            </description>
            <link>http://www.selleckchem.com/products/AT7867.html</link>
            <guid isPermaLink="false">4949AFD9-774E-4010-9A50-683603F54929</guid>
            <pubDate>Thu, 16 Dec 2010 09:19:43 +0800</pubDate>
        </item>
        <item>
            <title>BMS-740808 &gt;99%(HPLC) | (CAS 280118-23-2) | Factor Xa Inhibitor | BMS-740808</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/products/BMS-740808.html"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/BMS-740808.gif"></a><br />
Catalog NO.: <a href="http://www.selleckchem.com/products/BMS-740808.html">S1571</a><br />
Product: <a href="http://www.selleckchem.com/products/BMS-740808.html">BMS-740808</a><br />
Category:<a href="http://www.selleckchem.com/pharmacologicalact.html">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Others.html">Others</a> » <a href="http://www.selleckchem.com/pathways_Factor-Xa.html">Factor Xa</a> » <a href="http://www.selleckchem.com/products/BMS-740808.html">BMS-740808</a><br />
Biological Activity: BMS-740808 is a highly potent, selective, efficacious, and orally bioavailable blood coagulation factor Xa inhibitor with a Ki of 30 pM.]]>
            </description>
            <link>http://www.selleckchem.com/products/BMS-740808.html</link>
            <guid isPermaLink="false">AFBB2B18-C7D2-452A-A845-657F99F66F57</guid>
            <pubDate>Thu, 16 Dec 2010 09:56:42 +0800</pubDate>
        </item>
        <item>
            <title>BS-181 hydrochloride &gt;99%(HPLC) | (CAS N/A) | CDK Inhibitor | BS-181 hydrochloride</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/products/BS-181.html"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/BS-181%20hydrochloride.gif"></a><br />
Catalog No.: <a href="http://www.selleckchem.com/products/BS-181.html">S1572</a><br />
Product: <a href="http://www.selleckchem.com/products/BS-181.html">BS-181 hydrochloride</a><br />
Category: <a href="http://www.selleckchem.com/pharmacologicalact.html">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Cell-Cycle_Checkpoint.html">Cell Cycle/Checkpoint</a> » <a href="http://www.selleckchem.com/pathways_CDK.html">CDK</a>» <a href="http://www.selleckchem.com/products/BS-181.html">BS-181</a><br />
Biological Activity: BS-181 is a potent and selective CAK activity inhibitor with an IC50 of 21 nM.]]>
            </description>
            <link>http://www.selleckchem.com/products/BS-181.html</link>
            <guid isPermaLink="false">8B381823-2D55-41FF-8927-92DD3AC3C980</guid>
            <pubDate>Thu, 16 Dec 2010 10:15:37 +0800</pubDate>
        </item>
        <item>
            <title>Candesartan(Atacand) &gt;99%(HPLC) | (CAS 139481-59-7) | Angiotensin receptor Inhibitor | Atacand, Blopress, Amias, Ratacand, Candesartan(Atacand)</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/products/Candesartan%28Atacand%29.html"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/Candesartan.gif"></a><br />
Catalog No.:<a href="http://www.selleckchem.com/products/Candesartan%28Atacand%29.html">S1578</a><br />
Product: <a href="http://www.selleckchem.com/products/Candesartan%28Atacand%29.html">Candesartan(Atacand)</a><br />
Category: <a href="http://www.selleckchem.com/pharmacologicalact.html">By Product Pathways</a>» <a href="http://www.selleckchem.com/pharmacological_Others.html">Others</a> » <a href="http://www.selleckchem.com/pathways_ATR.html">ATR</a>» <a href="http://www.selleckchem.com/products/Candesartan%28Atacand%29.html">Candesartan(Atacand)</a><br />
Biological Activity: Candesartan is an angiotensin II receptor antagonist with an IC50 of 15 µg/kg.]]>
            </description>
            <link>http://www.selleckchem.com/products/Candesartan%28Atacand%29.html</link>
            <guid isPermaLink="false">43E7754C-7A6A-4927-B353-636163D27F7C</guid>
            <pubDate>Thu, 16 Dec 2010 10:41:19 +0800</pubDate>
        </item>
        <item>
            <title>Detomidine hydrochloride (Dormosedan) &gt;99%(HPLC) | (CAS 90038-01-0) | Order Online | Dormosedan, Detomidine hydrochloride (Dormosedan)</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/products/Detomidine-hydrochloride%28Dormosedan%29.html"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/Detomidine%20hydrochloride.gif"></a><br />
Catalog No.: <a href="http://www.selleckchem.com/products/Detomidine-hydrochloride%28Dormosedan%29.html">S1579</a><br />
Product: <a href="http://www.selleckchem.com/products/Detomidine-hydrochloride%28Dormosedan%29.html">Detomidine hydrochloride(Dormosedan)</a><br />
Category: <a href="http://www.selleckchem.com/researcharea.html">By Research Area</a> » <a href="http://www.selleckchem.com/research_Neurological-Disease.html">Neurological Disease</a> » <a href="http://www.selleckchem.com/products/Detomidine-hydrochloride%28Dormosedan%29.html">Detomidine hydrochloride(Dormosedan)</a><br />
Biological Activity: Detomidine hydrochloride is a nonnarcotic, synthetic alpha-2 adrenoreceptor agonist.]]>
            </description>
            <link>http://www.selleckchem.com/products/Detomidine-hydrochloride%28Dormosedan%29.html</link>
            <guid isPermaLink="false">A5C8EB0D-6552-4AC9-AB5C-8DAB27A61F2E</guid>
            <pubDate>Thu, 16 Dec 2010 10:36:34 +0800</pubDate>
        </item>
        <item>
            <title>Diclofensine (Ro 8-4650) &gt;99%(HPLC) | (CAS 67165-56-4) | Order Online | Diclofensine (Ro 8-4650)</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/products/Diclofensine%28Ro-8-4650%29.html"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/Diclofensine.gif"></a><br />
Catalog No.: <a href="http://www.selleckchem.com/products/Diclofensine%28Ro-8-4650%29.html">S1580</a><br />
Product: <a href="http://www.selleckchem.com/products/Diclofensine%28Ro-8-4650%29.html">Diclofensine(Ro 8-4650)</a><br />
Category: <a href="http://www.selleckchem.com/researcharea.html">By Research Area</a> » <a href="http://www.selleckchem.com/research_Neurological-Disease.html">Neurological Disease</a> » <a href="http://www.selleckchem.com/products/Diclofensine%28Ro-8-4650%29.html">Diclofensine(Ro 8-4650)</a><br />
Biological Activity: Diclofensine is a stimulant drug which acts as a triple reuptake inhibitor and a novel antidepressant]]>
            </description>
            <link>http://www.selleckchem.com/products/Diclofensine%28Ro-8-4650%29.html</link>
            <guid isPermaLink="false">89E54C0A-A01F-4B5F-9F8E-B3B953DFDE33</guid>
            <pubDate>Thu, 16 Dec 2010 10:33:03 +0800</pubDate>
        </item>
        <item>
            <title>Disulfiram (Antabuse) &gt;99%(HPLC) | (CAS 97-77-8) | Order Online | Antabuse, Antabus, Disulfiram (Antabuse)</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/products/Disulfiram%28Antabuse%29.html"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/ANTABUSE%20%28disulfiram%29.gif"></a><br />
Catalog No.: <a href="http://www.selleckchem.com/products/Disulfiram%28Antabuse%29.html">S1680</a><br />
Product: <a href="http://www.selleckchem.com/products/Disulfiram%28Antabuse%29.html">Disulfiram(Antabuse)</a><br />
Category: <a href="http://www.selleckchem.com/researcharea.html">By Research Area</a> » <a href="http://www.selleckchem.com/research_Neurological-Disease.html">Neurological Disease</a> » <a href="http://www.selleckchem.com/products/Disulfiram%28Antabuse%29.html">Disulfiram(Antabuse)</a><br />
Biological Activity: Disulfiram(Antabuse) is a drug used to support the treatment of chronic alcoholism by producing an acute sensitivity to alcohol.]]>
            </description>
            <link>http://www.selleckchem.com/products/Disulfiram%28Antabuse%29.html</link>
            <guid isPermaLink="false">E9D81FAB-5DB3-4CA1-9E5F-667F93942580</guid>
            <pubDate>Thu, 16 Dec 2010 09:44:40 +0800</pubDate>
        </item>
        <item>
            <title>KU-60019 &gt;99%(HPLC) | (CAS 925701-49-1) | ATM Inhibitor | KU-60019</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/products/KU-60019.html"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/KU-60019.gif"></a><br />
Catalog No.: <a href="http://www.selleckchem.com/products/KU-60019.html">S1570</a><br />
Product: <a href="http://www.selleckchem.com/products/KU-60019.html">KU-60019</a><br />
Category: <a href="http://www.selleckchem.com/pharmacologicalact.html">By Product Pathways</a> »<a href="http://www.selleckchem.com/pharmacological_Others.html">Othe</a>rs » <a href="http://www.selleckchem.com/pathways_ATM.html">ATM</a> » <a href="http://www.selleckchem.com/products/KU-60019.html">KU-60019</a><br />
Biological Activity: KU-60019 is 10-fold more effective than KU-55933 at blocking radiation-induced phosphorylation of key ATM targets in human glioma cells.]]>
            </description>
            <link>http://www.selleckchem.com/products/KU-60019.html</link>
            <guid isPermaLink="false">8EE72A93-8BCC-41ED-B97A-74A089063F4C</guid>
            <pubDate>Thu, 16 Dec 2010 10:46:39 +0800</pubDate>
        </item>
        <item>
            <title>Monobenzone (Benoquin) &gt;99%(HPLC) | (CAS 103-16-2) | Order Online | Benoquin, Monobenzone (Benoquin)</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/products/Monobenzone%28Benoquin%29.html"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/BENOQUIN%20%28monobenzone%29.gif"></a><br />
Catalog No.:<a href="http://www.selleckchem.com/products/Monobenzone%28Benoquin%29.html">S1652</a><br />
Product: <a href="http://www.selleckchem.com/products/Monobenzone%28Benoquin%29.html">Monobenzone(Benoquin)</a><br />
Category: <a href="http://www.selleckchem.com/researcharea.html">By Research Area</a> » <a href="http://www.selleckchem.com/research_Metabolic-Disease.html">Metabolic Disease</a> » <a href="http://www.selleckchem.com/products/Monobenzone%28Benoquin%29.html">Monobenzone(Benoquin)</a><br />
Biological Activity: Monobenzone(Benoquin) is a compound used as a topical drug for medical depigmentation.]]>
            </description>
            <link>http://www.selleckchem.com/products/Monobenzone%28Benoquin%29.html</link>
            <guid isPermaLink="false">E6DA73CF-EF9D-42B9-B68C-549075A5F70B</guid>
            <pubDate>Thu, 16 Dec 2010 09:39:16 +0800</pubDate>
        </item>
        <item>
            <title>Nepicastat (SYN117) &gt;99%(HPLC) | (CAS 173997-05-2) | Order Online | SYN117, RS-25560-197, Nepicastat (SYN117)</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/products/Nepicastat%28SYN117%29.html"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/Nepicastat.gif"></a><br />
Catalog No.:<a href="http://www.selleckchem.com/products/Nepicastat%28SYN117%29.html">S1583</a><br />
Product:<a href="http://www.selleckchem.com/products/Nepicastat%28SYN117%29.html">Nepicastat(SYN117)</a><br />
Category: <a href="http://www.selleckchem.com/researcharea.html">By Research Area »</a> <a href="http://www.selleckchem.com/research_Cardiovascular-Disease.html">Cardiovascular Disease</a> » <a href="http://www.selleckchem.com/products/Nepicastat%28SYN117%29.html">Nepicastat(SYN117)</a><br />
Biological Activity: Nepicastat is a dopamine beta-hydroxylase inhibitor with IC50 of 8.5 ± 0.8 and 9.0 ± 0.8 nM for bovine and human, respectively.]]>
            </description>
            <link>http://www.selleckchem.com/products/Nepicastat%28SYN117%29.html</link>
            <guid isPermaLink="false">EBB87566-BE65-4D2E-97F1-6FFD93654C2F</guid>
            <pubDate>Thu, 16 Dec 2010 10:19:02 +0800</pubDate>
        </item>
        <item>
            <title>PD318088 &gt;99%(HPLC) | (CAS 391210-00-7 ) | MEK Inhibitor | PD318088</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/products/PD318088.html"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/PD318088.gif"></a><br />
Catalog No.: <a href="http://www.selleckchem.com/products/PD318088.html">S1568</a><br />
Product: <a href="http://www.selleckchem.com/products/PD318088.html">PD318088</a><br />
Category: <a href="http://www.selleckchem.com/pharmacologicalact.html">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_MAPK.html">MAPK</a> »<a href="http://www.selleckchem.com/pathways_MEK.html">MEK</a> » <a href="http://www.selleckchem.com/products/PD318088.html">PD318088</a><br />
Biological Activity: PD318088 is a non-ATP competitive allosteric MEK1/2 inhibitor.]]>
            </description>
            <link>http://www.selleckchem.com/products/PD318088.html</link>
            <guid isPermaLink="false">60EA5350-8D31-401F-B26E-D33734483EEC</guid>
            <pubDate>Thu, 16 Dec 2010 10:12:18 +0800</pubDate>
        </item>
        <item>
            <title>PHT-427 &gt;99%(HPLC) | (CAS 1191951-57-1) | Akt Inhibitor | PDK-1 Inhibitor | PHT427, PHT 427, PHT-427</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/products/PHT-427.html"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/PHT-427.gif"></a><br />
Catalog No.: <a href="http://www.selleckchem.com/products/PHT-427.html">S1556</a><br />
Product: <a href="http://www.selleckchem.com/products/PHT-427.html">PHT-427</a><br />
Category: <a href="http://www.selleckchem.com/pharmacologicalact.html">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_PI3K_Akt_mTOR.html">PI3K/Akt/mTOR</a> » <a href="http://www.selleckchem.com/pathways_Akt.html">Akt</a> » <a href="http://www.selleckchem.com/products/PHT-427.html">PHT-427</a><br />
Biological Activity: HT-427 is a Novel Akt/phosphatidylinositide-dependent protein kinase 1 pleckstrin homology domain inhibitor.]]>
            </description>
            <link>http://www.selleckchem.com/products/PHT-427.html</link>
            <guid isPermaLink="false">F3D491C1-D404-4153-8E6C-CBF11EF6CD99</guid>
            <pubDate>Thu, 16 Dec 2010 09:29:21 +0800</pubDate>
        </item>
        <item>
            <title>Ramipril (Altace) &gt;99%(HPLC) | (CAS 87333-19-5) | Ras Inhibitor | Ramipro, Tritace, Altace, Prilace, Ramipril (Altace)</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/products/Ramipril%28Altace%29.html"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/ALTACE%20%28ramipril%29.gif"></a><br />
Catalog No.: <a href="http://www.selleckchem.com/products/Ramipril%28Altace%29.html">S1793</a><br />
 Product: <a href="http://www.selleckchem.com/products/Ramipril%28Altace%29.html">Ramipril(Altace)</a><br />
Category: <a href="http://www.selleckchem.com/pharmacologicalact.html">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_MAPK.html">MAPK</a> »<a href="http://www.selleckchem.com/pathways_Ras.html">Ras</a> » <a href="http://www.selleckchem.com/products/Ramipril%28Altace%29.html">Ramipril(Altace)</a><br />
Biological Activity: Ramipril(Altace) is an angiotensin-converting enzyme (ACE) inhibitor with an IC50 of 5 nM.]]>
            </description>
            <link>http://www.selleckchem.com/products/Ramipril%28Altace%29.html</link>
            <guid isPermaLink="false">64C5C21E-57A4-4E0B-A760-E15B44FDDB31</guid>
            <pubDate>Thu, 16 Dec 2010 09:52:22 +0800</pubDate>
        </item>
        <item>
            <title>Ranolazine (Ranexa) &gt;99%(HPLC) | (CAS 95635-55-5) | Order Online | Ranexa, Ranolazine (Ranexa)</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/products/Ranolazine%28Ranexa%29.html"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/RANEXA%20%28ranolazine%29.gif"></a><br />
Catalog No.: <a href="http://www.selleckchem.com/products/Ranolazine%28Ranexa%29.html">S1799</a><br />
Product: <a href="http://www.selleckchem.com/products/Ranolazine%28Ranexa%29.html">Ranolazine(Ranexa</a>)<br />
Category: <a href="http://www.selleckchem.com/researcharea.html">By Research Area</a> » <a href="http://www.selleckchem.com/research_Cardiovascular-Disease.html">Cardiovascular Disease</a> » <a href="http://www.selleckchem.com/products/Ranolazine%28Ranexa%29.html">Ranolazine(Ranexa)</a><br />
Biological Activity: Ranolazine(Ranexa) is an antianginal medication.]]>
            </description>
            <link>http://www.selleckchem.com/products/Ranolazine%28Ranexa%29.html</link>
            <guid isPermaLink="false">845063C7-C208-40B3-879F-8BBE2B3FFDA4</guid>
            <pubDate>Thu, 16 Dec 2010 09:48:09 +0800</pubDate>
        </item>
        <item>
            <title>Ubenimex (Bestatin) &gt;99%(HPLC) | (CAS 58970-76-6) | Aminopeptidase Inhibitor | Bestatin, Ubenimex (Bestatin)</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/products/Ubenimex%28Bestatin%29.html"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/Ubenimex.gif"></a><br />
Catalog No.: <a href="http://www.selleckchem.com/products/Ubenimex%28Bestatin%29.html">S1591</a><br />
Product: <a href="http://www.selleckchem.com/products/Ubenimex%28Bestatin%29.html">Ubenimex(Bestatin)</a><br />
Category:<a href="http://www.selleckchem.com/pharmacologicalact.html">By Product Pathways</a> » <a href="http://www.selleckchem.com/pharmacological_Proteases_HSP90_HSP70.html">Proteases/HSP90/HSP70</a> » <a href="http://www.selleckchem.com/pathways_Aminopeptidase.html">Aminopeptidase</a> » <a href="http://www.selleckchem.com/products/Ubenimex%28Bestatin%29.html">Ubenimex(Bestatin)</a><br />
Biological Activity: Ubenimex is a competitive aminopeptidase B inhibitor with an IC50 of 100 mg/ml for K562 cells.]]>
            </description>
            <link>%3Ca%20href=%22http://www.selleckchem.com/products/Ubenimex%28Bestatin%29.html%22%3E%3Cimg%20alt=%22%22%20border=%220%22%20src=%22http://www.selleckchem.com/pic/digi/Ubenimex.gif%22%3E%3C/a%3E%3Cbr%20/%3E%20Catalog%20No.:%20%3Ca%20href=%22http://www.selleckchem.com/products/Ubenimex%28Bestatin%29.html%22%3ES1591%3C/a%3E%3Cbr%20/%3E%20Product:%20%3Ca%20href=%22http:/http://www.selleckchem.com/products/Ubenimex%28Bestatin%29.html</link>
            <guid isPermaLink="false">AB8D807F-FB2B-4DF6-A840-4C32AEBEF077</guid>
            <pubDate>Thu, 16 Dec 2010 10:53:10 +0800</pubDate>
        </item>
        <item>
            <title>Vidarabine (Vira-A) &gt;99%(HPLC) | (CAS 5536-17-4) | Order Online | Vira-A, Vidarabine (Vira-A)</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/products/Vidarabine%28Vira-A%29.html"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/VIRA-A%20%28vidarabine%29.gif"></a><br />
Catalog No.: <a href="http://www.selleckchem.com/products/Vidarabine%28Vira-A%29.html">S1784</a><br />
Product: <a href="http://www.selleckchem.com/products/Vidarabine%28Vira-A%29.html">Vidarabine(Vira-A)</a><br />
Category: <a href="http://www.selleckchem.com/researcharea.html">By Research Area</a> »<a href="http://www.selleckchem.com/research_Infection.html">Infection</a> » <a href="http://www.selleckchem.com/products/Vidarabine%28Vira-A%29.html">Vidarabine(Vira-A)</a><br />
Biological Activity: Vidarabine(Vira-A) is an antiviral drug which is active against herpes simplex and varicella zoster viruses.]]>
            </description>
            <link>http://www.selleckchem.com/products/Vidarabine%28Vira-A%29.html</link>
            <guid isPermaLink="false">A96F6AE3-66CF-48BE-904C-D0897BEF3B44</guid>
            <pubDate>Thu, 16 Dec 2010 11:02:37 +0800</pubDate>
        </item>
        <item>
            <title>VX-809 &gt;99%(HPLC) | (CAS 936727-05-8) | Order Online | VX809, VX 809, VX-809</title>
            <description>
                <![CDATA[<a href="http://www.selleckchem.com/products/VX-809.html"><img alt="" border="0" src="http://www.selleckchem.com/pic/digi/VX-809.gif"></a><br />
Catalog No.:<a href="http://www.selleckchem.com/products/VX-809.html">S1565</a><br />
Product: <a href="http://www.selleckchem.com/products/VX-809.html">VX-809</a><br />
Category: <a href="http://www.selleckchem.com/researcharea.html">By Research Area</a> » <a href="http://www.selleckchem.com/research_Immunology.html">Immunology</a> »<a href="http://www.selleckchem.com/products/VX-809.html">VX-809</a><br />
Biological Activity: VX-809 is the second investigational oral drug candidate for the treatment of cystic fibrosis (CF).]]>
            </description>
            <link>http://www.selleckchem.com/products/VX-809.html</link>
            <guid isPermaLink="false">0AF2CBE4-C196-42F7-BD7C-7E5931E3C612</guid>
            <pubDate>Thu, 16 Dec 2010 09:36:06 +0800</pubDate>
        </item>
    </channel>
</rss>

