Synthesis and structure–Activity relationships of aroylpyrrole alkylamide bradykinin (B2) antagonists
摘要:
The synthesis and structure-activity relationships of a novel series of aroylpyrrole alkylamindes as potent selective bradykinin 132 receptor antagonists are described. Several members of this series display nanomolar affinity at the B-2 receptor and show activity in an animal model of antinociception. (C) 2003 Elsevier Science Ltd. All rights reserved.
[EN] NOVEL HETEROARYL ALKYLAMIDE DERIVATIVES USEFUL AS BRADYKININ RECEPTOR MODULATORS<br/>[FR] NOUVEAUX DERIVES HETEROARYLALKYLAMIDE UTILES EN TANT QUE MODULATEURS DU RECEPTEUR DE LA BRADYKININE
申请人:——
公开号:WO2003087090A3
公开(公告)日:2003-12-11
NOVEL HETEROARYL ALKYLAMIDE DERIVATIVES USEFUL AS BRADYKININ RECEPTOR MODULATORS
申请人:Ortho-McNeil Pharmaceutical, Inc.
公开号:EP1495017A2
公开(公告)日:2005-01-12
US6958349B2
申请人:——
公开号:US6958349B2
公开(公告)日:2005-10-25
US7358261B2
申请人:——
公开号:US7358261B2
公开(公告)日:2008-04-15
Novel heteroaryl alkylamide derivatives useful as bradykinin receptor modulators
申请人:——
公开号:US20040192720A1
公开(公告)日:2004-09-30
This invention is directed towards novel alkylamide derivatives as bradykinin receptor antagonists useful for the treatment of bradykinin modulated disorders such as pain, inflammation, asthma and allergy. Furthermore, the present invention is directed to novel alkylamide derivatives as bradykinin receptor agonists useful for the treatment of bradykinin modulated disorders such as hypertension and the like.