Name | indoloazepine |
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Description | Chk2-IN-1 (compound 1) is a potent and selective inhibitor of checkpoint kinase 2 (Chk2), with IC50s of 13.5 nM and 220.4 nM for Chk2 and Chk1, respectively. Chk2-IN-1 can elicit a strong ataxia telangiectasia mutated (ATM)-dependent Chk2-mediated radioprotection effect[1]. |
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Related Catalog | |
Target |
Chk2:13.5 nM (IC50) Chk1:220.4 nM (IC50) |
References |
Molecular Formula | C15H13N5O2 |
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Molecular Weight | 295.29600 |
Exact Mass | 295.10700 |
PSA | 112.37000 |
LogP | 1.25050 |