Title : The preclinical pharmacology and therapeutic activity of the novel CHK1 inhibitor SAR-020106.

Pub. Date : 2010 Jan

PMID : 20053762






1 Functional Relationships(s)
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1 SAR-020106 is an ATP-competitive, potent, and selective CHK1 inhibitor with an IC(50) of 13.3 nmol/L on the isolated human enzyme. Adenosine Triphosphate sarcosine dehydrogenase Homo sapiens