2-Isopropyl-5-methyl-1-(2,6-dihydroxy-4-nonylphenyl)cyclohex-1-ene
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2-Isopropyl-5-methyl-1-(2,6-dihydroxy-4-nonylphenyl)cyclohex-1-ene
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| Systematic (IUPAC) name | |
| 2-Isopropyl-5-methyl-1-(2,6-dihydroxy-4-nonylphenyl)cyclohex-1-ene | |
| Clinical data | |
| Pregnancy cat. | ? |
| Legal status | ? |
| Identifiers | |
| ATC code | ? |
| Chemical data | |
| Formula | C25H40O2 |
| Mol. mass | 372.582 g/mol |
| SMILES | eMolecules & PubChem |
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2-Isopropyl-5-methyl-1-(2,6-dihydroxy-4-nonylphenyl)cyclohex-1-ene is an analgesic compound which is a cannabinoid agonist. It is a ring-opened cannabinoid derivative, an analogue of cannabidiol. However, unlike cannabidiol, this compound produces potent cannabis-like effects in animals, suggesting it acts as a CB1 agonist.[1]
It can be synthesized by Birch reduction from the nonyl-analog of cannabidiol.[2]
References
- ^ Razdan, K. (1981). "The Total Synthesis of Cannabinoids". In John Apsimon. The Total Synthesis of Natural Products. Wiley Interscience. p. 245. ISBN 978-0-471-05460-3. OCLC 19487018.
- ^ Razdan RK, Pars HG, Thompson WR, Granchelli FE (1974). "Lithium-ammonia reduction of tetrahydrocannabinols". Tetrahedron Letters 15 (49–50): 4315. doi:10.1016/S0040-4039(01)92152-5.
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