Catalog |
name |
Description |
price |
R-C-2681 |
Amonafide CAS: 69408-81-7 |
Amonafide is a topoisomerase II inhibitor and DNA intercalator that induces apoptotic signaling by blocking the binding of Topo II to DNA. |
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R-C-2682 |
CRT0044876 CAS:6960-45-8 |
CRT0044876 is a potent BER inhibitor or DNA Base Excision Repair Pathway Inhibitor (APE1 IC50-3 microM).CRT0044876 potentiates the cytotoxicity of several DNA base-targeting compounds,with accumulation of apurinic sites. |
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R-C-2694 |
BYK 204165 CAS:1104546-89-5 |
BYK204165 is a potent and selective PARP1 inhibitor. BYK204165 inhibits cell-free recombinant human PARP-1(hPARP-1)with a pIC50 of 7.35(pKi=7.05),and murine PARP-2(mPARP-2)with a pIC50 of 5.38,respectively.BYK204165 displays 100-fold selectivity for PARP-1. |
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R-R-4425 |
AZD1390 CAS No.2089288-03-7 |
AZD1390/CAS No.2089288-03-7 is a potent, highly selective, orally bioavailable, brain-penetrant ATM inhibitor with an IC50 of 0.78 nM in cell. |
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R-R-4426 |
Camonsertib CAS No.2417489-10-0 |
Camonsertib (RP-3500)/CAS No.2417489-10-0 is an orally active, selective ATR kinase inhibitor (ATRi) with an IC50 of 1.00 nM in biochemical assays. Camonsertib shows 30-fold selectivity for ATR over mTOR (IC50=120 nM) and >2,000-fold selectivity over ATM, DNA-PK, and PI3Kα kinases. Camonsertib has potent antitumor activity. |
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R-C-2727 |
GSK 0660 CAS:1014691-61-2 |
GSK 0660 is a selective PPARβ antagonist(IC50 values are 0.155,>10 and≥10µM at PPARβ,PPARα and PPARγ respectively). |
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R-R-4427 |
Elimusertib hydrochloride |
Elimusertib (BAY 1895344) hydrochloride is a potent, orally active and selective ATR inhibitor with an IC50 of 7 nM. Elimusertib hydrochloride has anti-tumor activity. Elimusertib hydrochloride can be used for the research of solid tumors and lymphomas. |
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R-R-4428 |
Gartisertib CAS No.1613191-99-3 |
Gartisertib (VX-803)/CAS No.1613191-99-3 is an ATP-competitive, orally active, and selective ATR inhibitor, with a Ki of <150 pM. Gartisertib potently inhibits ATR-driven phosphorylated checkpoint kinase-1 (Chk1) phosphorylation with an IC50 of 8 nM. Antitumor activity. |
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R-R-4429 |
Tuvusertib CAS No.1613200-51-3 |
Tuvusertib (M1774; ATR inhibitor 1)/CAS No.1613200-51-3 is a selective and orally active ATR inhibitor extracted from patent WO2015187451A1, compound I-l, with a Ki value below 1 μΜ. |
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R-R-4430 |
Lartesertib CAS No.2495096-26-7 |
Lartesertib (M4076)/CAS No.2495096-26-7 is a potent inhibitor of serine/threonine protein kinase ATM (extracted from patent WO2022058351A1). |
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