Potency and safety analysis of hemp-derived delta-9 products: The hemp vs. cannabis demarcation problem
Contents
Appearance
Names | |
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IUPAC name
5-Hydroxy-2-methyl-2-(4-methylpent-3-enyl)-7-pentylchromene-6-carboxylic acid
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Other names
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Identifiers | |
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3D model (JSmol)
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ChEBI |
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ChEMBL |
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ChemSpider |
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PubChem CID
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UNII |
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CompTox Dashboard (EPA)
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Properties | |
C22H30O4 | |
Molar mass | 358.478 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Cannabichromenic acid (CBCA) is minor cannabinoid and precursor of cannabichromene.[2]
Biosynthesis
Geranyl pyrophosphate and olivetolic acid combine to produce cannabigerolic acid (CBGA; the sole intermediate for all other phytocannabinoids). The enzyme CBCA synthase can cyclize either cannabigerolic acid or cannabinerolic acid (the Z isomer of CBGA) to form CBCA.[3]
See also
References
- ^ "KNApSAcK Metabolite Information - C00053033". www.knapsackfamily.com.
- ^ Shoyama Y, Fujita T, Yamauchi T, Nishioka I (June 1968). "Cannabichromenic acid, a genuine substance of cannabichromene". Chemical & Pharmaceutical Bulletin. 16 (6): 1157–8. doi:10.1248/cpb.16.1157. PMID 5706836.
- ^ Morimoto S, Komatsu K, Taura F, Shoyama Y (November 1998). "Purification and characterization of cannabichromenic acid synthase from Cannabis sativa". Phytochemistry. 49 (6): 1525–9. doi:10.1016/s0031-9422(98)00278-7. PMID 9862135.