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S1166
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Cisplatin |
Cisplatin is an inorganic and water-soluble platinum complex, which is able to inhibit DNA synthesis by conforming DNA adducts. |
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S1215
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Carboplatin |
Carboplatin is a DNA synthesis inhibitor by binding to DNA and interfering with the cell's repair mechanism. |
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S1149
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Gemcitabine HCl (Gemzar) |
Gemcitabine Hydrochloride (Gemzar) is a DNA synthesis inhibitor with IC50 of 50 nM, 40 nM, 18 nM and 12 nM in PANC1, MIAPaCa2, BxPC3 and Capan2 cells, respectively. |
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S1224
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Oxaliplatin (Eloxatin) |
Oxaliplatin inhibits DNA synthesis by conforming DNA adducts. |
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S1229
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Fludarabine Phosphate (Fludara) |
Fludarabine Phosphate is an analogue of adenosine and deoxyadenosine, which is able to compete with dATP for incorporation into DNA and inhibit DNA synthesis. |
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S1491
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Fludarabine (Fludara) |
Fludarabine (Fludara, F-ara-A, NSC 118218) is a STAT1 activation inhibitor and a DNA synthesis inhibitor. |
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S1135
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Pemetrexed (Alimta) |
Pemetrexed disodium (Alimta) is a novel antifolate and antimetabolite for TS, DHFR and GARFT with Ki of 1.3 nM, 7.2 nM and 65 nM, respectively. |
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S1270
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CCT239065 |
CCT239065 is a novel and selective BRAFV600E and LCK inhibitor with IC50 of 13 nM and 6 nM, respectively. |
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S2029
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Uridine |
Uridine is a nucleoside, contains a uracil attached to a ribose ring via a β-N1-glycosidic bond.
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S1981
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Adenine |
Adenine is a purine derivative and a nucleobase with a variety of roles in biochemistry. |
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S1983
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Adenine HCl |
Adenine hydrochloride is a hydrochloride salt form of adenine which is a purine derivative and a nucleobase with a variety of roles in biochemistry. |
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S1982
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Adenine sulfate |
Adenine sulfate is a sulfate salt form of adenine which is a purine derivative and a nucleobase with a variety of roles in biochemistry. |
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S1995
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Procarbazine HCl (Matulane) |
Procarbazine hydrochloride (Matulane) is a hydrochloride salt form of procarbazine which is a polyfunctional alkylating compound used as an antineoplastic agent. |
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S2678
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NSC-207895 (XI-006) |
NSC-207895 suppresses MDMX with IC50 of 2.5 µM, leading to enhanced p53 stabilization/activation and DNA damage. |
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S2684
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CX-5461 |
CX-5461 selectively inhibits Pol I-driven transcription of rRNA with IC50 of 142 nM in HCT-116 cells. |
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S2554
|
Daphnetin |
Daphnetin is an inhibitor of EGFR, PKA and PKC with IC50 of 7.67 μM, 9.33 μM and 25.01 μM, respectively. |
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S1648
|
Cytarabine |
Cytarabine (Cytosine arabinoside, AraC) is an antimetabolic agent and DNA synthesis inhibitor with IC50 of 16 nM in wild-type CCRF-CEM cells. |
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S1782
|
Azacitidine(Vidaza) |
Azacitidine is a nucleoside analogue of cytidine that specifically inhibits DNA methylation by trapping DNA methyltransferases. |
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S1221
|
Dacarbazine (DTIC-Dome) |
Dacarbazine(DTIC-Dome) is an antineoplastic chemotherapy drug used in the treatment of various cancers. |
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S1714
|
Gemcitabine(Gemzar) |
Gemcitabine(Gemzar) belongs to the group of medicines called antimetabolites. |
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S1384
|
Mizoribine (Bredinin) |
Mizoribine (Bredinin) is an imidazole nucleoside and an immunosuppressive agent with an IC50 of approximately 100 μM. |
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S1334
|
Flupirtine maleate |
Flupirtine maleate is the salt form of Flupirtine, which is a non-opioid, centrally acting analgesia, muscle relaxation and neuroprotection. |
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S1299
|
Floxuridine (Fludara) |
Floxuridine (Fludara) is a prodrugs of floxuridine and an oncology agent with an GI50 of 5.1 μM for the inhibition of MDCK/PEPT1. |
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S1300
|
Ftorafur |
Ftorafur is a substance being used in the treatment of some types of cancer. |
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S1302
|
Ifosfamide |
Ifosfamide is a nitrogen mustard alkylating agent used in the treatment of cancer. |
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S1305
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Mercaptopurine |
Mercaptopurine is a widely used antileukemic agent and immunosuppressive drug that inhibits de novo purine synthesis through incorporation of thiopurine methyltransferase metabolites into DNA and RNA. |
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S1289
|
Carmofur |
Carmofur (INN) is a pyrimidine analogue used as an antineoplastic agent. |
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S1213
|
Nelarabine (Arranon) |
Nelarabine (Arranon, 506U78) is a purine nucleoside analog and DNA synthesis inhibitor with IC50 from 0.067-2.15 μM in tumor cells. |
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S1214
|
Bleomycin sulfate |
Bleomycin sulfate (Blenoxane) is a glycopeptide antibiotic and an anticancer agent for squamous cell carcinomas (SCC) with IC50 of 4 nM in UT-SCC-19A cells. |
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S1217
|
Clafen (Cyclophosphamide) |
This agent inhibited cell proliferation of NCI-H727 with IC50 at 9.3 nM. |
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S1218
|
Clofarabine |
Clofarabine inhibits the enzymatic activities of ribonucleotide reductase (IC50 = 65 nM) and DNA polymerase |
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S1209
|
Adrucil(Fluorouracil) |
Adrucil (Fluorouracil) is an DNA/RNA synthesis inhibitor, which interrupts nucleotide synthetic by inhibiting thymidylate synthase (TS). |
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S1199
|
Cladribine |
Cladribine (Leustatin, Litak, 2CDA) is an adenosine deaminase inhibitor for U266, RPMI8226, and MM1.S cells with IC50 of approximately 2.43 μM, 0.75 μM, and 0.18 μM, respectively. |
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S1192
|
Raltitrexed (Tomudex) |
Raltitrexed (Tomudex) is a thymidylate synthase inhibitor with an IC50 of 9 nM for the inhibition of L1210 cell growth. |
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S1156
|
Capecitabine (Xeloda) |
Capecitabine is a tumor-selective fluoropyrimidine carbamate which achieves higher intratumoral 5-FU level with lower toxicity than 5-FU. |
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