名称:
Potent bradykinin B1 receptor antagonists: 4-Substituted phenyl cyclohexanes
摘要:
Selective bradykinin (BK) B-1 receptor antagonists have been shown to be antinociceptive in animal models and could be novel therapeutic agents for the treatment of pain and inflammation. Elucidation of the structure-activity relationships of the biphenyl moiety of the lead compound 1 provided a potent new structural class of BK B-1 receptor antagonists. (C) 2007 Elsevier Ltd. All rights reserved.
DOI:
10.1016/j.bmcl.2007.03.059