开始日期2014-04-01 |
申办/合作机构 |
开始日期2013-09-01 |
申办/合作机构 |
开始日期2012-09-01 |
申办/合作机构 |
Extensive structure–activity studies on three different modification sites resulted in a series of LIM kinase inhibitors, containing a novel tricyclic hinge-binding motif based on the pyrrolopyrimidine scaffold.