Optimization of triaryl bis-sulfones as cannabinoid-2 receptor ligands
摘要:
Structure-activity relationship on our recently reported triaryl bis-sulfone class of cannabinoid-2 (C132) receptor selective inverse agonists was explored. Modifications to the methane sulfonamide, substitutions to B and C phenyl rings, and replacements of the C-ring were investigated. A compound with excellent C132 activity, selectivity for C132 over CB I, and in vivo plasma levels was identified. (c) 2007 Elsevier Ltd. All rights reserved.
[EN] CANNABINOID RECEPTOR LIGANDS<br/>[FR] LIGANDS DU RECEPTEUR CANNABINOIDE
申请人:SCHERING CORP
公开号:WO2004014825A1
公开(公告)日:2004-02-19
The invention relates to compounds of the formula, a prodrug thereof, or a pharmaceutically acceptable salt, solvate or stereoisomer of the compound or of said prodrug; which exhibit anti-inflammatory and immunodulatory activity. Also disclosed are pharmaceutical compositions containing said compounds and methods of using the compounds for the treatment of various diseases and conditions.
[EN] CANNABINOID RECEPTOR LIGANDS<br/>[FR] LIGANDS DES RECEPTEURS CANNABINOIDES
申请人:SCHERING CORP
公开号:WO2002062750A1
公开(公告)日:2002-08-15
There are disclosed compounds of the formula (I) a prodrug thereof, or a pharmaceutically acceptable salt, solvate or stereoisomer of the compound or of said prodrug; which exhibit anti-inflammatory and immunodulatory activity. Also disclosed are pharmaceutical compositions containing said compounds and methods of using the compounds for the treatment of various diseases and conditions.