Abeo-HHC acetate
Semi-synthetic derivative of THC
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| Identifiers | |
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| CAS Number |
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| Chemical and physical data | |
| Formula | C23H34O3 |
| Molar mass | 358.522 g·mol−1 |
| 3D model (JSmol) |
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InChI
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Abeo-HHC acetate is a semi-synthetic derivative of tetrahydrocannabinol, first described in the 1980s. It is synthesised from delta-11-tetrahydrocannabinol, which can be made to undergo a ring expansion reaction via a hydrazone intermediate.[1][2] It is structurally similar to HHC-acetate except that the methylated cyclohexyl ring has been replaced by a cycloheptane.
See also
- Cis-THC
- Cycloheptyl CP 55,940
- Hexahydrocannabinol
- Iso-THC
- O-1656
- THC-O-acetate
References
- ^ Srebnik M, Mechoulam R (1984). "Reactions of cannabinoid tosylhydrazones: Stereochemical aspects". Tetrahedron. 40 (19): 3839–3843. doi:10.1016/S0040-4020(01)88815-3.
- ^ Ujváry I (June 2023). "Hexahydrocannabinol and closely related semi-synthetic cannabinoids: A comprehensive review". Drug Testing and Analysis. doi:10.1002/dta.3519. PMID 37269160. S2CID 259046522.
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| Active metabolites |
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- 2-Arachidonyl glyceryl ether (2-AGE; noladin ether)
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- O-Arachidonoyl ethanolamine (O-AEA; virodhamine)
cannabinoid
receptor
agonists /
neocannabinoids
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enhancers
(inactivation inhibitors)
- 4-Nonylphenylboronic acid
- AM-404
- Arachidonoyl serotonin
- Arvanil
- BIA 10-2474
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(antagonists/inverse
agonists/antibodies)
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- Hemopressin
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- MK-9470
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- O-1918
- O-2050
- O-2654
- Otenabant (CP-945,598)
- PF-514273
- PipISB
- PSB-SB-487
- Rimonabant (SR141716)
- Rosonabant (E-6776)
- SR-144,528
- Surinabant (SR147778)
- Taranabant (MK-0364)
- TM-38837
- VCHSR
- See also: Cannabinoid receptor modulators (cannabinoids by pharmacology)
- List of: AM cannabinoids
- JWH cannabinoids
- Designer drugs § Synthetic cannabimimetics
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