Title : Structure-based generation of a new class of potent Cdk4 inhibitors: new de novo design strategy and library design.

Pub. Date : 2001 Dec 20

PMID : 11741479






1 Functional Relationships(s)
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1 By constructing diarylurea informer libraries based on the structural requirements of Cdk inhibitors in the ATP binding pocket of the Cdk4 model, we were able to identify a potent Cdk4 inhibitor N-(9-oxo-9H-fluoren-4-yl)-N"-pyridin-2-ylurea 15 (IC(50) = 0.10 microM), together with preliminary SAR. Adenosine Triphosphate sarcosine dehydrogenase Homo sapiens