申请人:Devadas Balekudru
公开号:US20090270350A1
公开(公告)日:2009-10-29
This invention is directed generally to substituted pyridinone and pyrimidinone compounds that generally inhibit p38 kinase, TNF, and/or cyclooxygeπase activity. Such substituted pyridinone and pyrimidinone compounds include compounds generally corresponding in structure to the following formula: wherein Z, n, R
1
, R
2a
, R
2b
, R
2c
, R
2d
, R
2e
, R
3a
, R
3b
, R
3c
, R
3d
, R
4
, R
5
, R
6
, R
7a
, R
7b
, R
7c
, R
7d
and R
7e
are as defined in this specification. This invention also is directed to compositions of such substituted pyridinones and pyrimidinones (particularly pharmaceutical compositions), and methods for treating disorders (typically pathological disorders) associated with p38 kinase activity, TNF activity, and/or cyclooxygenase-2 activity.
本发明通常涉及取代的吡啶酮和嘧啶酮化合物,它们通常抑制p38激酶、TNF和/或环氧合酶活性。这些取代的吡啶酮和嘧啶酮化合物包括通常对应于以下结构公式的化合物:其中Z、n、R1、R2a、R2b、R2c、R2d、R2e、R3a、R3b、R3c、R3d、R4、R5、R6、R7a、R7b、R7c、R7d和R7e如本说明书所定义。本发明还涉及这些取代的吡啶酮和嘧啶酮(特别是药物组成物)的组成物,以及用于治疗与p38激酶活性、TNF活性和/或环氧合酶-2活性相关的疾病(通常是病理性疾病)的方法。