Isoxazolone based inhibitors of p38 MAP kinases

被引:36
|
作者
Laufer, Stefan A. [1 ]
Margutti, Simona [1 ]
机构
[1] Univ Tubingen, Dept Pharmaceut & Med Chem, Inst Pharm, D-72076 Tubingen, Germany
关键词
D O I
10.1021/jm701343f
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
SAR of N-alkylated isoxazolones as p38 MAP kinase inhibitors was realized. The data herein show the possibility of transferring the SAR study and evaluation from N-1-substituted imidazole to isoxazolones. Optimization of substituent was realized.
引用
收藏
页码:2580 / 2584
页数:5
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