Piperazinyl CCR1 antagonists - optimization of human liver microsome stability

被引:14
作者
Brown, Matthew F. [1 ]
Bahnck, Kevin B. [1 ]
Blumberg, Laura C. [1 ]
Brissette, William H. [1 ]
Burrell, Sara A. [1 ]
Driscoll, James P. [1 ]
Fedeles, Flavia [1 ]
Fisher, Michael B. [1 ]
Foti, Robert S. [1 ]
Gladue, Ronald P. [1 ]
Guzman-Martinez, Aikomari [1 ]
Hayward, Matthew M. [1 ]
Lira, Paul D. [1 ]
Lillie, Brett M. [1 ]
Lu, Y. [1 ]
Lundquist, Greg D. [1 ]
McElroy, Eric B. [1 ]
McGlynn, Molly A. [1 ]
Paradis, Timothy J. [1 ]
Poss, Christopher S. [1 ]
Roache, James H. [1 ]
Shavnya, Andrei [1 ]
Shepard, Richard M. [1 ]
Trevena, Kristen A. [1 ]
Tylaska, Laurie A. [1 ]
机构
[1] Pfizer Global Res & Dev, Groton, CT 06340 USA
关键词
BX471; CP-481715; CCR1; antagonist;
D O I
10.1016/j.bmcl.2007.03.037
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The synthesis, biological activity, and pharmacokinetic profile of CCR1 antagonists are described. (C) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3109 / 3112
页数:4
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