Description
CB-
52 is a stable analog of Δ
9-
tetrahydrocannabinol (THC) and anandamide (AEA). It exhibits high affinity for the central cannabinoid (CB
1) and peripheral cannabinoid (CB
2) receptors with K
i values of 210 and 30 nM, respectively.
1 In vitro, CB-
52 behaves primarily as a CB
1 receptor partial agonist and a CB
2 receptor neutral antagonist.
2
References
1. Brizzi, A., Brizzi, V., Cascio, M.G., et al. Design, synthesis, and binding studies of new potent ligands of cannabinoid receptors J. Med. Chem. 48,7343-7350(2005).
2. Cascio, M.G., Bisogno, T., Palazzo, E., et al. In vitro and in vivo pharmacology of synthetic olivetol- or resorcinol-derived cannabinoid receptor ligands Br. J. Pharmacol. 149,431-440(2006).