Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12779/5600
Title: New Resorcinol-Anandamide "Hybrids" as Potent Cannabinoid Receptor Ligands Endowed with antinociceptive activity in vivo
Authors: Brizzi, Antonella 
Brizzi, Vittorio
Cascio, M. G.
Corelli, Federico 
Guida, F.
Ligresti, A.
Maione, S.
Martinelli, A
Pasquini, S.
Tuccinardi, T.
Di Marzo, V.
Issue Date: 2009
Project: None 
Journal: JOURNAL OF MEDICINAL CHEMISTRY
Abstract: 
Bearing in mind the pharmacophoric requirements of both (-)-trans-Delta(9)-tetrahydrocannabinol (THC) and anandamide (AEA), we designed a novel pharmacophore consisting of both a rigid aromatic backbone and a flexible chain with the aim to develop a series of stable and potent ligands of cannabinoid receptors. In this paper we report the synthesis, docking studies, and structure-activity relationships of new resorcinol-anandamide "hybrids" differing in the side chain group. Compounds bearing a 2-methyloctan-2-yl group at position 5 showed a significantly higher affinity for cannabinoid (CB) receptors, in particular when an alkyloxy chain of 7 or 10 carbon atoms was also present at position 1. Derivative 32 was a potent CB(1) and CB(2) ligand, with K(i) values similar to that of WIN 55-212 and potent antinociceptive activity in vivo. Moreover, derivative 38, although less potent, proved to be the most selective ligand for CB(2) receptor (K(i)(CB(1)) = 1 muM, K(i)(CB(2)) = 35 nM).
Description: 
38711
URI: http://hdl.handle.net/20.500.12779/5600
ISSN: 0022-2623
DOI: 10.1021/jm8016255
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