Trends in Kinase Selectivity: Insights for Target Class-Focused Library Screening

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• 作者：Shana L. Posy ; Mark A. Hermsmeier ; Wayne Vaccaro ; Karl-Heinz Ott ; Gordon Todderud ; Jonathan S. Lippy ; George L. Trainor ; Deborah A. Loughney ; Stephen R. Johnson
• 刊名：Journal of Medicinal Chemistry
• 出版年：2011
• 出版时间：January 13, 2011
• 年：2011
• 卷：54
• 期：1
• 页码：54-66
• 全文大小：1344K
• 年卷期：v.54,no.1(January 13, 2011)
• ISSN：1520-4804

文摘

A kinome-wide selectivity screen of >20000 compounds with a rich representation of many structural classes has been completed. Analysis of the selectivity patterns for each class shows that a broad spectrum of structural scaffolds can achieve specificity for many kinase families. Kinase selectivity and potency are inversely correlated, a trend that is also found in a large set of kinase functional data. Although selective and nonselective compounds are mostly similar in their physicochemical characteristics, we identify specific features that are present more frequently in compounds that bind to many kinases. Our results support a scaffold-oriented approach for building compound collections to screen kinase targets.