Design, synthesis and activity of a potent, selective series of N-aryl pyridinone inhibitors of p38 kinase

被引:13
|
作者
Selness, Shaun R. [1 ]
Boehm, Terri L. [1 ]
Walker, John K. [1 ]
Devadas, Balekudru [1 ]
Durley, Richard C. [1 ]
Kurumbail, Ravi [2 ]
Shieh, Huey [2 ]
Xing, Li [2 ]
Hepperle, Michael [1 ]
Rucker, Paul V. [1 ]
Jerome, Kevin D. [1 ]
Benson, Alan G. [1 ]
Marrufo, Laura D. [1 ]
Madsen, Heather M. [1 ]
Hitchcock, Jeff [1 ]
Owen, Tom J. [1 ]
Christie, Lance [1 ]
Promo, Michele A. [1 ]
Hickory, Brian S. [1 ]
Alvira, Edgardo [1 ]
Naing, Win [1 ]
Blevis-Bal, Radhika [1 ]
Devraj, Rajesh V. [1 ]
Messing, Dean [3 ]
Schindler, John F. [4 ]
Hirsch, Jeffrey [4 ]
Saabye, Matthew [4 ]
Bonar, Sheri [4 ]
Webb, Elizabeth [4 ]
Anderson, Gary [4 ]
Monahan, Joseph B. [2 ,4 ]
机构
[1] Pfizer Corp, Dept Med Chem, Chesterfield, MO 63017 USA
[2] Pfizer Corp, Struct & Computat Chem, Chesterfield, MO 63017 USA
[3] Pfizer Corp, Dept Pharmcokinet & Drug Metab, Chesterfield, MO 63017 USA
[4] Pfizer Corp, Inflammat Biol, Chesterfield, MO 63017 USA
关键词
p38; kinase; Inflammation; Rheumatoid arthritis; TNF alpha; Pyridinones; RHEUMATOID-ARTHRITIS;
D O I
10.1016/j.bmcl.2011.04.120
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A series of N-aryl pyridinone inhibitors of p38 mitogen activated protein (MAP) kinase were designed and prepared based on the screening hit SC-25028 (1) and structural comparisons to VX-745 (5). The focus of the investigation targeted the dependence of potency and metabolic stability on the benzyloxy connectivity, the role of the C-6 position and the substitution pattern on the N-phenyl ring. Further optimization produced the highly selective and potent pyridinones 2 and 3. These inhibitors exhibited activity in both acute and chronic models of inflammation. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4059 / 4065
页数:7
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