Novel Mps1 kinase inhibitors: From purine to pyrrolopyrimidine and quinazoline leads

被引:15
|
作者
Bursavich, Matthew G. [1 ]
Dastrup, David [1 ]
Shenderovich, Mark [1 ]
Yager, Kraig M. [1 ]
Cimbora, Daniel M. [2 ]
Williams, Brandi [2 ]
Kumar, D. Vijay [1 ]
机构
[1] Myrexis Inc, Med Chem, Salt Lake City, UT 84108 USA
[2] Myrexis Inc, Vitro Pharmacol, Salt Lake City, UT 84108 USA
关键词
Mps1; TTK; Protein kinase inhibitors; Scaffold hopping; Conformational restriction; Structure-based design; Cancer; Purines; Pyrrolopyrimidines; Quinazoline; POTENT;
D O I
10.1016/j.bmcl.2013.10.008
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Mps1, also known as TTK, is a mitotic checkpoint protein kinase that has become a promising new target of cancer research. In an effort to improve the lead-likeness of our recent Mps1 purine lead compounds, a scaffold hopping exercise has been undertaken. Structure-based design, principles of conformational restriction, and subsequent scaffold hopping has led to novel pyrrolopyrimidine and quinazoline Mps1 inhibitors. These new single-digit nanomolar leads provide the basis for developing potent, novel Mps1 inhibitors with improved drug-like properties. (C) 2013 Elsevier Ltd. All rights reserved.
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页码:6829 / 6833
页数:5
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