Novel Adamantyl Cannabinoids as CB1 Receptor Probes

作者：Thakur Ganesh A^*; Bajaj Shama; Paronis Carol; Peng Yan; Bowman Anna L; Barak Lawrence S; Caron Marc G; Parrish Demon; Deschamps Jeffrey R; Makriyannis Alexandros

来源：Journal of Medicinal Chemistry, 2013, 56(10): 3904-3921.

DOI：10.1021/jm4000775

In previous studies, compound 1 (AM411), a 3-(1-adamantyl) analogue of the phytocannabinoid (-)-Delta(8)-tetrahydrocannabinol (Delta(8)-THC), was shown to have improved affinity and selectivity for the CB1 receptor. In this work, we further explored the role of the 1-adamantyl group at the C-3 position in a series of tricyclic cannabinoid analogues modified at the 9-northern aliphatic hydroxyl (NAH) position. Of these, 9-hydroxymethyl hexahydrocannabinol 11 (AM4054) exhibited high CB1 affinity and full agonist profile. In the cAMP assay, the 9-hydroxymethyl cannabinol analogue 24 (AM4089) had a partial agonist profile, with high affinity and moderate selectivity for rCB1 over hCB2. In vivo results in rat models of hypothermia and analgesia were congruent with in vitro data. Our in vivo data indicate that 3-(1-adamantyl) substitution, within NAH cannabinergics, imparts improved pharmacological profiles when compared to the corresponding, traditionally used 3-dimethylheptyl analogues and identifies 11 and 24 as potentially useful in vivo CB1 cannabinergic probes.

• 出版日期2013-5-23
• 单位东北大学