Kinesin spindle protein (KSP) inhibitors. Part 1: The discovery of 3,5-diaryl-4,5-dihydropyrazoles as potent and selective inhibitors of the mitotic kinesin KSP

被引:132
作者
Cox, CD
Breslin, MJ
Brenda, JM
Coleman, PJ
Buser, CA
Walsh, ES
Hamilton, K
Huber, HE
Kohl, NE
Torrent, M
Yan, YW
Kuo, LC
Hartman, GD
机构
[1] Merck Res Labs, Dept Med Chem, W Point, PA 19486 USA
[2] Merck Res Labs, Dept Canc Res, W Point, PA 19486 USA
[3] Merck Res Labs, Dept Mol Syst, W Point, PA 19486 USA
[4] Merck Res Labs, Dept Biol Struct, W Point, PA 19486 USA
关键词
KSP; mitotic kinesins; anti-mitotics; dihydropyrazoles;
D O I
10.1016/j.bmcl.2005.02.055
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Optimization of high-throughput screening (HTS) hits resulted in the discovery of 3,5-diaryl-4,5-dihydropyrazoles as potent and selective inhibitors of KSP. Dihydropyrazole 15 is a potent, cell-active KSP inhibitor that induces apoptosis and generates aberrant mitotic spindles in human ovarian carcinoma cells at low nanomolar concentrations. X-ray crystallographic evidence is presented which demonstrates that these inhibitors bind in an allosteric pocket of KSP distant from the nucleotide and microtubule binding sites. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2041 / 2045
页数:5
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