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.
The invention relates to compounds of the formula
1
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.
Optimization of triaryl bis-sulfones as cannabinoid-2 receptor ligands
作者:Brian J. Lavey、Joseph A. Kozlowski、Bandarpalle B. Shankar、James M. Spitler、Guowei Zhou、De-Yi Yang、Youheng Shu、Michael K.C. Wong、Shing-Chun Wong、Neng-Yang Shih、Jie Wu、Stuart W. McCombie、Razia Rizvi、Ronald L. Wolin、Charles A. Lunn
DOI:10.1016/j.bmcl.2007.04.028
日期:2007.7
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.