Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10588312 | Bioorganic & Medicinal Chemistry Letters | 2012 | 6 Pages |
Abstract
Cannabinoid CB1 receptor agonists exhibit potent analgesic effects in rodents and humans, but their clinical utility as analgesic drugs is often limited by centrally mediated side effects. We report herein the preparation of N-methyl-3-(tetrahydro-2H-pyran-4-yl)-2,3,4,9-tetrahydro-1H-carbazole-6-carboxamides as a novel class of hCB1/hCB2 dual agonists with attractive physicochemical properties. More specifically, (R)-N,9-dimethyl-N-(4-(methylamino)-4-oxobutyl)-3-(tetrahydro-2H-pyran-4-yl)-2,3,4,9-tetrahydro-1H-carbazole-6-carboxamide, displayed an extremely low level of CNS penetration (Rat Cbr/Cplasma = 0.005 or 0.5%) and was devoid of CNS side effects during pharmaco-dynamic testing.
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Zhongyong Wei, Hua Yang, Ziping Liu, Maxime Tremblay, Shawn Johnstone, Sara Béha, Shi Yi Yue, Sanjay Srivastava, Miroslaw J. Tomaszewski, William Brown, Christopher Walpole, Stéphane St-Onge, Etienne Lessard, Anne-Julie Archambault, Thierry Groblewski,