Chk2-IN-1 (compound 1) is a potent and selective inhibitor of checkpoint kinase 2 (Chk2) , with IC 50 s 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.
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