HU-243
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| Formula | C25H40O3 |
| Molar mass | 388.592 g·mol−1 |
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HU-243 (AM-4056) is a synthetic cannabinoid drug that is a single enantiomer of the hydrogenated derivative of the commonly used reference agonist HU-210. It is a methylene homologue of canbisol. It is a potent agonist at both the CB1 and CB2 receptors, with a binding affinity of 0.041 nM at the CB1 receptor, making it marginally more potent than HU-210, which had an affinity of 0.061 nM in the same assay.[1]
With an affinityvalue of 0.043nM, this cannabinoide is ranged in the most potent (synthetic) cannabinoids. But there are more potent cannabinoids with the chemical structure of the JWH-cannabinoids (JWh-250, and JWH-210) which are demonstrating affinityvalues up to 0.000952- and 0.00654nM in respective. JWH-015 ranges in the nanomolar ability of HU-210- and 250 with 0.068nM slightly above HU-210 its potency (0.061nM).[2] so the signatory countries to these international drug control treaties are not required by said treaties to control HU-243.
- ^ Stern E, Lambert DM (August 2007). "Medicinal chemistry endeavors around the phytocannabinoids". Chemistry & Biodiversity. 4 (8): 1707–28. doi:10.1002/cbdv.200790149. PMID 17712816. S2CID 24920412.
- ^ https://www.unodc.org/unodc/en/commissions/CND/conventions.html |title=UN International Drug Control Conventions |access-date=2017-02-15 |archive-date=2018-01-12 |archive-url=https://web.archive.org/web/20180112202649/https://www.unodc.org/unodc/en/commissions/CND/conventions.html |url-status=dead