HU-243

HU-243
Identifiers
IUPAC name
  • (6aR,8S,9S,10aR)-9-(hydroxymethyl)-6,6-dimethyl-3-(2-methyloctan-2-yl)-8,9-ditritio-7,8,10,10a-tetrahydro-6aH-benzo[c]chromen-1-ol
CAS Number
PubChem CID
IUPHAR/BPS
UNII
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC25H40O3
Molar mass388.592 g·mol−1
3D model (JSmol)
SMILES
  • CC(O1)(C)[C@H]2[C@@H](C[C@H](CO)CC2)C3=C1C=C(C(C)(C)CCCCCC)C=C3O

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.

  1. ^ 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.
  2. ^ 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