Capped diaminopropionamide–glycine dipeptides are inhibitors of CC chemokine receptor 2 (CCR2)
摘要:
A new series of CCR2 antagonists has been discovered that incorporates intramolecular hydrogen bonding as a strategy for rigidifying the scaffold. The structure-activity relationship was established through initial systematic modification of substitution pattern and chain length, followed by independent optimization of three different substituents (benzylamine, carboxamide, and benzamide). Several of the acyclic compounds display 10-30 nM binding affinity for CCR2. Moreover, these antagonists are able to block both MCP-1-induced Ca2+ flux and monocyte chemotaxis, and are selective for binding to CCR2 over CCR1 and CCR3. (C) 2007 Elsevier Ltd. All rights reserved.
Diamines as modulators of chemokine receptor activity
申请人:——
公开号:US20030060459A1
公开(公告)日:2003-03-27
The present application describes modulators of MCP-1 of formula (I):
1
or pharmaceutically acceptable salt forms thereof, useful for the prevention of asthma, multiple sclerosis, artherosclerosis, and rheumatoid arthritis.
DIAMINES AS MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY
申请人:Bristol-Myers Squibb Pharma Company
公开号:EP1351924A2
公开(公告)日:2003-10-15
US6974836B2
申请人:——
公开号:US6974836B2
公开(公告)日:2005-12-13
US7449493B2
申请人:——
公开号:US7449493B2
公开(公告)日:2008-11-11
[EN] DIAMINES AS MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY<br/>[FR] DIAMINES SERVANT DE MODULATEURS DE L'ACTIVITÉ RÉCEPTEUR DES CHIMIOKINES
申请人:BRISTOL MYERS SQUIBB PHARMA CO
公开号:WO2002050019A2
公开(公告)日:2002-06-27
The present application describes modulators of MCP-1 of formula (I): or pharmaceutically acceptable salt forms thereof, useful for the prevention of asthma, multiple sclerosis, atherosclerosis, and rheumatoid arthritis.