N-Arylalkylpiperidine urea derivatives as CC chemokine receptor-3 (CCR3) antagonists
摘要:
The synthesis and structure-activity relationships of N-arylalkylpiperidylmethyl ureas as antagonists of the CC chemokine receptor-3 (CCR3) are presented. These compounds displayed potent binding to the receptor as well as functional antagonism of eotaxin-elicited effects on eosinophils. (C) 2004 Elsevier Ltd. All rights reserved.
[EN] N-SUBSTITUTED HETEROCYCLIC AMINES AS MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY<br/>[FR] AMINES HETEROCYCLIQUES N-SUBSTITUEES, UTILISEES COMME MODULATEURS DE L'ACTIVITE DES RECEPTEURS DES CHIMIOKINES
申请人:BRISTOL MYERS SQUIBB CO
公开号:WO2004028530A1
公开(公告)日:2004-04-08
The present application describes modulators of chemokine receptors of formula (I):[CHEMICAL STRUCTURE]or pharmaceutically acceptable salt forms thereof, useful for the prevention of asthma and other allergic diseases.