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Hexahydrocannabiphorol

Semi-sythetic cannabinoid drug From Wikipedia, the free encyclopedia

Commonly misspelled as 'hexahydroxycannabiphorol'

CAS Number
FormulaC23H36O2
Molar mass344.539 g·mol−1
Quick facts Identifiers, CAS Number ...
Hexahydrocannabiphorol
Identifiers
  • (6aR,10aR)-6,6,9-trimethyl-3-heptyl-6a,7,8,9,10,10a-hexahydrobenzo[c]chromen-1-ol
CAS Number
Chemical and physical data
FormulaC23H36O2
Molar mass344.539 g·mol−1
3D model (JSmol)
  • CCCCCCCc1cc2OC(C)(C)[C@@H]3CCC(C)C[C@H]3c2c(O)c1
  • InChI=InChI=1S/C23H36O2/c1-5-6-7-8-9-10-17-14-20(24)22-18-13-16(2)11-12-19(18)23(3,4)25-21(22)15-17/h14-16,18-19,24H,5-13H2,1-4H3/t16?,18-,19-/m1/s1
  • Key:USZILQYXSONCHH-VOBHOPKGSA-N
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Hexahydrocannabiphorol (HHCP) is a semi-synthetic cannabinoid derivative which has been marketed since around 2021.[1][2] It is believed to be made from the hydrogenation of tetrahydrocannabiphorol (THCP). THCP is only reported as a trace component of cannabis in 2019.[3] HHCP was studied by Roger Adams as early as 1942.[4]

Pharmacology

HHC-P is a partial agonist of the CB1 receptors with an EC50 of 44.4nM for 9R-HHCP and 134nM for 9S-HHCP. Compared to Hexahydrocannabinol (HHC) with an EC50 of 101nM for 9R-HHC and 1,190nM for 9S-HHC.[5] In 2021, HHC-P was positively identified in multiple gray market cannabis products in the United States.[1]

Legality

The legal status of hexahydrocannabinol and derivatives varies between countries, leading to widespread sale in some parts of Europe and the US.

In France, HHCP was banned in 2023.[6]

In Japan, Japanese Health Ministry announced that six synthetic cannabinoids with structures similar to HHCH, including HHCP, were to be banned from 6 January 2024.[7]

HHCP was banned in Slovakia as of 13 January 2024.[citation needed]

See also

References

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