Cannabicyclol
From Wikipedia, the free encyclopedia
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Cannabicyclol
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| Systematic (IUPAC) name | |
| (1aR-(1a alpha,3a alpha,8b alpha,8c alpha))- 1a,2,3,3a, 8b,8c-hexahydro-1,1,3a-trimethyl -6- pentyl-1H-4-oxabenzo (f)cyclobut(cd)inden-8-ol |
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| Identifiers | |
| CAS number | ? |
| ATC code | ? |
| PubChem | |
| Chemical data | |
| Formula | C21H30O2 |
| Mol. mass | 314.462 g/mol |
| Pharmacokinetic data | |
| Bioavailability | ? |
| Metabolism | ? |
| Half life | ? |
| Excretion | ? |
| Therapeutic considerations | |
| Pregnancy cat. |
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| Legal status | |
| Routes | ? |
Cannabicyclol, also known as CBL, is a non-psychedelic cannabinoid found in the Cannabis species. CBL is a degradative product like Cannabinol. Light converts Cannabichromene to CBL.
CDB in Cannabis is known to induce sleep. The Cannabis Indica strain contains overall more CBL than Cannabis Sativa strains.
[edit] See also
[edit] Notes
[edit] External links & References
- CTD's Cannabicyclol page from the Comparative Toxicogenomics Database
- Erowid Compounds found in Cannabis sativa
- http://www.wiley-vch.de/stmdata/pdf/CompoundList.pdf
- http://www.a1b2c3.com/drugs/mj028.htm
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