2014 Dec 4;6(2):198-203. doi: 10.1021/ml500439x. eCollection 2015.
El Bakali J1, Muccioli GG2, Body-Malapel M3, Djouina M3, Klupsch F1, Ghinet A1, Barczyk A1, Renault N1, Chavatte P1, Desreumaux P3, Lambert DM2, Millet R1.
Abstract
The CB2 cannabinoid receptor has been implicated in the regulation of intestinal inflammation. Following on from the promising activity of a series of 4-oxo-1,4-dihydroquinoline-3-carboxamide, we developed constrained analogues based on a 2H-pyrazolo[4,3-c]quinolin-3(5H)-one scaffold, with improved affinity for the hCB2 receptor and had very high selectivity over the hCB1 receptor. Importantly, the lead of this series (26, hCB2: K i = 0.39 nM, hCB1: K i > 3000 nM) was found to protect mice against experimental colitis after oral administration.
KEYWORDS:
Cannabinoid receptor; colitis; conformational restriction; endocannabinoid; inflammatory bowel disease; quinolone
- PMID:
- 25699149
- [PubMed]