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Mammalian target of rapamycin
| Cat.No. | Product Name | Feedback | Added |
|---|---|---|---|
| S1555 | AZD8055 | Oct 2010 | |
| AZD8055 is a potent, selective, and orally bioavailable ATP-competitive mTOR kinase inhibitor with an IC50 of 0.8 nM. | |||
| S1009 | BEZ235 (NVP-BEZ235) | Apr 2009 | |
| BEZ235 (NVP-BEZ235) is a dual ATP-competitive phosphatidylinositol 3-kinase (PI3K) and mammalian target of rapamycin (mTOR) inhibitor with an IC50 of 4, 5, 7 and 75 nM for p110α, p110γ, p110δ and p110β, respectively. | |||
| S2406 | Chrysophanic acid (Chrysophanol) | Mar 2011 | |
| Chrysophanic acid (Chrysophanol) is a EGFR/mTOR pathway inhibitor. | |||
| S1022 | Deforolimus (Ridaforolimus) | Apr 2009 | |
| Deforolimus (Ridaforolimus) is a small-molecule inhibitor of mTOR. | |||
| S1120 | Everolimus (RAD001) | Sep 2009 | |
| Everolimus (RAD001) also known as SDZ-RAD, Certican, Zortress, Afinitorm is MTOR inhibitor available at Selleck with IC50 of 0.63 nM. | |||
| S2696 | GDC-0980 (RG7422) | Nov 2011 | |
| 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. | |||
| S1360 | GSK1059615 | Jun 2010 | |
| GSK1059615 is a pan-PI3K reversible inhibitor,IC50:PI3Kα(0.4 nM), β (0.6 nM),γ (5 nM),δ (2 nM) and mTOR(12 nM). | |||
| S2658 | GSK2126458 | Aug 2011 | |
| GSK2126458 is a highly potent PI3K and mTOR inhibitor with an app Ki of 19 pM for PI3K. | |||
| S1226 | KU-0063794 | May 2010 | |
| Ku-0063794 is a mTOR inhibitor, IC50 ~10 nM for mTORC1 and mTORC2, respectively. | |||
| S2638 | NU7441 | Aug 2011 | |
| NU7441 is a potent and selective DNA-dependent protein kinase (DNA-PK) inhibitor with IC50 of 0.01, 1.7 and 5 μM for DNA-PK, mTOR and PI 3-K, respectively. | |||
| S2624 | OSI-027 | Jun 2011 | |
| OSI027 is a potent mammalian target of rapamycin (mTOR) kinase inhibitor. | |||
| S2238 | Palomid 529 (P529) | May 2011 | |
| Palomid 529 (P529) is a novel potent antitumour PI3K/Akt/mTOR inhibitor with a GI50 of <35 μM in the NCI-60 cell lines panel. | |||
| S2743 | PF-04691502 | Jan 2012 | |
| PF-04691502 is a potent and selective dual PI3K/mTOR inhibitor to phosphorylation of AKT T308 and AKT S473 with IC50 of 7.5 and 3.8 nM, respectively. | |||
| S1038 | PI-103 | Apr 2009 | |
| PI-103 is a potent, cell-permeable, ATP-competitive PI3K family members inhibitor with IC50 of 2, 8, 20, 26, 48, 83, 88, 150 nM for DNA-PK, p110α, mTORC1, PI3-KC2β, p110δ, mTORC2, p110β, and p110γ, respectively. | |||
| S2628 | PKI-587 | Jul 2011 | |
| PKI-587 is a highly potent dual PI3K/mTOR kinase inhibitor with IC50 of 0.4 nM and <0.1 μM for PI3K-α and mTOR, respectively. | |||
| S2218 | PP242 | Apr 2011 | |
| PP242 is a novel potent and selective mTOR inhibitor with an IC50 of 8 nM. | |||
| S1039 | Rapamycin (Sirolimus) | Apr 2009 | |
| Rapamycin also known as Sirolimus & Rapamune is a mTOR inhibitor. Rapamycin Sirolimus inhibits cell motility by suppression of mTOR-mediated pathways. | |||
| S1044 | Temsirolimus (Torisel) | Apr 2009 | |
| Temsirolimus (Torisel) is a mTOR inhibitor. | |||
| S2689 | WAY-600 | Aug 2011 | |
| WAY-600 is a potent ATP-competitive mTOR inhibitor with an IC50 of 9 nM. | |||
| S2661 | WYE-125132 | Aug 2011 | |
| WYE-125132 is a highly potent, ATP-competitive and specific mTOR kinase inhibitor with an IC50 of 0.19 nM. | |||
| S1266 | WYE-354 | Jun 2010 | |
| WYE-354 is a mTOR inhibitor with an IC50 of 5 nM. | |||
| S2668 | WYE-687 | Aug 2011 | |
| WYE-687 is a potent ATP-competitive mTOR inhibitor with an IC50 of 7 nM. | |||
| S1523 | XL765 | Oct 2010 | |
| XL765 is a mixed mTOR/PI3k inhibitor with IC50 of 157, 39, 113, 9 and 43 nM for mTOR, p110α, β, γ and δ, respectively. | |||
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Customer's Feedback
| Dongfeng Chen, The Rausing Lab |
| "Your product U0126(Cat.NO S1102) works well in our experiments. I hope I can get more excellent products from your company in future." |
| R.B. Cambridge |
| "I have used the chemical that I bought from you(Selleck,PTC-124) and it worked well.So we will eventually be ordering more." |
| Zhenghe John Wang Assistant Professor, Case Western Reserve University |
| "We have purchased LBH-589, Saha and MS-275 from you and they all worked well." |
| Jenny Sun |
| "We used the LBH-589 in our experiments. The compound is easy to use with excellent reproducibility." |
| Yu Wang, Harvard University |
| "The GDC0449 compound worked very well. The results in my hands are equally good as what's been published. Thanks for this great resource for our research." |
| Dung-Fang Lee |
| "Based on our preliminary data, I found MLN8237 and VX-680 have good effects in inhibiting Aurka-maintaining ESC self-renewal in mouse ES cells." |
Latest Catalog
| May 2010 Selleck Latest Catalog | ![]() |

