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3-Acyl-2,6-diaminopyridines as cyclin-dependent kinase inhibitors: synthesis and biological evaluation
Authors:Lin Ronghui  Lu Yanhua  Wetter Steven K  Connolly Peter J  Turchi Ignatius J  Murray William V  Emanuel Stuart L  Gruninger Robert H  Fuentes-Pesquera Angel R  Adams Mary  Pandey Niranjan  Moreno-Mazza Sandra  Middleton Steven A  Jolliffe Linda K
Affiliation:Johnson & Johnson Pharmaceutical Research & Development L.L.C., Drug Discovery, 1000 Route 202, Raritan, New Jersey 08869, USA. rlin@prdus.jnj.com
Abstract:A novel series of 2,6-diamino-3-acylpyridines were designed and synthesized as cyclin-dependent kinase (CDK) inhibitors. The representative compounds 2r and 11 showed potent CDK1 and CDK2 inhibitory activities and inhibited cellular proliferation in HeLa, HCT116, and A375 tumor cells.
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