化学
组蛋白脱乙酰基酶
组蛋白脱乙酰酶抑制剂
酶抑制剂
组蛋白
药理学
立体化学
生物化学
酶
DNA
医学
作者
Paul L. Wash,Timothy Z. Hoffman,Brandon M. Wiley,Céline Bonnefous,Nicholas D. Smith,Michael S. Sertic,C. Martin Lawrence,Kent T. Symons,Phan-Manh Nguyen,Kevin D. Lustig,Xin Guo,Tami Annable,Stewart A. Noble,Jeffrey H. Hager,Christian A. Hassig,James W. Malecha
标识
DOI:10.1016/j.bmcl.2008.10.058
摘要
In an effort to discover novel non-hydroxamic acid histone deacetylase (HDAC) inhibitors, a novel alpha-mercaptoketone was identified in a high-throughput screen. Lead optimization of the screening hit, led to a number of potent HDAC inhibitors. In particular, alpha-mercaptoketone 19y (KD5150) exhibited nanomolar in vitro activity and inhibition of tumor growth in vivo.
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