Substituted dipiperidine alcohols as potent CCR2 antagonists
摘要:
The synthesis and biological evaluation of a series of substituted dipiperidine alcohols are described. Structure-activity relationship studies led to the discovery of potent CCR2 antagonists displaying IC(50) values in the nanomolar or subnanomolar range. The cinnamoyl compounds had higher binding affinities than the corresponding urea analogs. (C) 2008 Elsevier Ltd. All rights reserved.
DOI:
10.1016/j.bmcl.2008.05.010
作为产物:
描述:
在
lithium aluminium tetrahydride 作用下,
生成
参考文献:
名称:
Substituted dipiperidine alcohols as potent CCR2 antagonists
摘要:
The synthesis and biological evaluation of a series of substituted dipiperidine alcohols are described. Structure-activity relationship studies led to the discovery of potent CCR2 antagonists displaying IC(50) values in the nanomolar or subnanomolar range. The cinnamoyl compounds had higher binding affinities than the corresponding urea analogs. (C) 2008 Elsevier Ltd. All rights reserved.