Cas No. |
Product name |
136164-66-4 |
CRT0044876 |
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CRT0044876 is a potent and selective APE1 inhibitor with IC50 of ~3 μM. |
896705-16-1 |
BMH-21 |
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BMH-21 is a small molecule DNA intercalator that binds ribosomal DNA and inhibits RNA polymerase I (Pol I) transcription; does not cause phosphorylation of H2AX. |
1533426-72-0 |
SCR7 |
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SCR7 is a molecule that inhibits joining of DSBs in cell-free repair system; inhibits NHEJ(nonhomologous end-joining) in a Ligase IV-dependent manner within cells, and activa... |
57852-57-0 |
Idarubicin HCl |
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Idarubicin HCl is a hydrochloride salt form of Idarubicin which is an anthracycline antibiotic and a DNA topoisomerase II (topo II) inhibitor for MCF-7 cells with IC50 of 3.3... |
1609960-30-6 |
TH287 |
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TH287 is a potent inhibitor of MTH1 (NUDT1) with an IC50 value of 0.8 nM, less potent for MTH2, NUDT5, NUDT12, NUDT14, and NUDT16. |
72496-41-4 |
Pirarubicin |
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Pirarubicin is an anthracycline antibiotic, and also a DNA/RNA synthesis inhibitor by intercalating into DNA and interacts with topoisomerase II, used as an antineoplastic ag... |
175414-77-4 |
Voreloxin(SNS-595; AG 7352) |
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Voreloxin is a potent Topoisomerase II inhibitor with broad-spectrum anti-tumor activity. |
259793-96-9 |
Favipiravir(T-705) |
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Favipiravir (T-705) is a potent and selective RNA-dependent RNA polymerase inhibitor, used to treat influenza virus infections. |
210829-30-4 |
Gemcitabine elaidate(CP-4126; CO-101) |
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Gemcitabine elaidate(CP-4126; CO-101) is the combination of Gemcitabine and saturated fatty acid derivatives, and highly lipophilic anticancer activity. |
1048371-03-4 |
UPF 1069 |
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UPF 1069 is a selective PARP2 inhibitor with IC50 of 0.3 μM. It is ~27-fold selective against PARP1. |