| Literature DB >> 17532631 |
Ronghui Lin1, Peter J Connolly, Yanhua Lu, George Chiu, Shengjian Li, Yang Yu, Shenlin Huang, Xun Li, Stuart L Emanuel, Steven A Middleton, Robert H Gruninger, Mary Adams, Angel R Fuentes-Pesquera, Lee M Greenberger.
Abstract
A series of 3,5-disubstituted pyrazolo[3,4-b]pyridine cyclin-dependent kinase (CDK) inhibitors was synthesized. These compounds showed potent and selective CDK inhibitory activities and inhibited in vitro cellular proliferation in cultured human tumor cells. Selected compounds were evaluated in an in vivo tumor xenograft model. The synthesis and biological evaluation of these pyrazolo[3,4-b]pyridines and related compounds are reported.Entities:
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Year: 2007 PMID: 17532631 DOI: 10.1016/j.bmcl.2007.05.029
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823