Aminopyridinecarboxamide-based inhibitors: Structure-activity relationship

被引:5
|
作者
Bonafoux, Dominique F. [1 ]
Bonar, Sheri L. [2 ]
Clare, Michael [1 ]
Donnelly, Ann M. [2 ]
Glaenzer, Jeanette L. [1 ]
Guzova, Julia A. [2 ]
Huang, He [1 ]
Kishore, Nandidni N. [2 ]
Koszyk, Francis J. [1 ]
Lennon, Patrick J. [1 ]
Libby, Adam [1 ]
Mathialagan, Sumathy [2 ]
Oburn, David S. [1 ]
Rouw, Sharon A. [2 ]
Sommers, Cynthia D. [2 ]
Tripp, Catherine S. [2 ]
Vanella, Lori J. [2 ]
Weier, Richard [1 ]
Wolfson, Serge G. [1 ]
Huang, Horng-Chih [1 ]
机构
[1] Pfizer Inc, Dept Med Chem, St Louis, MO 63017 USA
[2] Pfizer Inc, Dept Biol, St Louis, MO 63017 USA
关键词
IKK2; NFkB; Inhibitor; NF-KAPPA-B; IKK-2; INHIBITOR; DISCOVERY;
D O I
10.1016/j.bmc.2009.10.040
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Series of aminopyridinecarboxamide-based inhibitors were synthesized and tested against human recombinant IKK-2 and in IL-1 beta stimulated synovial. broblasts. The 2-amino-5-chloropyridine-4-carboxamides were identified as the most potent inhibitors with improved cellular activity. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:403 / 414
页数:12
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