Synthesis and SAR of p38α MAP kinase inhibitors based on heterobicyclic scaffolds
作者:T.G. Murali Dhar、Stephen T. Wrobleski、Shuqun Lin、Joseph A. Furch、David S. Nirschl、Yi Fan、Gordon Todderud、Sidney Pitt、Arthur M. Doweyko、John S. Sack、Arvind Mathur、Murray McKinnon、Joel C. Barrish、John H. Dodd、Gary L. Schieven、Katerina Leftheris
DOI:10.1016/j.bmcl.2007.07.029
日期:2007.9
The synthesis and structure-activity relationships (SAR) of p38 alpha MAP kinase inhibitors based on heterobicyclic scaffolds are described. This effort led to the identification of compound (21) as a potent inhibitor of p38a MAP kinase with good cellular potency toward the inhibition of TNF-alpha production. X-ray co-crystallography of an oxalamide analog (24) bound to unphosphorylated p38 alpha is also disclosed. (c) 2007 Elsevier Ltd. All rights reserved.
US7943617B2
申请人:——
公开号:US7943617B2
公开(公告)日:2011-05-17
US8309571B2
申请人:——
公开号:US8309571B2
公开(公告)日:2012-11-13
HETEROBICYCLIC COMPOUNDS USEFUL AS KINASE INHIBITORS
申请人:Dhar T.G. Murali
公开号:US20080275052A1
公开(公告)日:2008-11-06
A compound of Formula (I)
and enantiomers, diastereomers and pharmaceutically-acceptable salts thereof. Also disclosed are pharmaceutical compositions containing compounds of Formula I, and methods of treating conditions associated with the activity of p38 kinase.