Publication | Closed Access
Biosynthesis of cannabinoids
169
Citations
20
References
2001
Year
Food ChemistryCannabis UseBiosynthesisBiochemistryMedicineC 10Cannabis SativaNatural Product BiosynthesisQuantitative Nmr SpectroscopyPhytochemistryPharmacologyCannabinoid PharmacologyCannabinoidsNatural Product Synthesis
The biosynthesis of cannabinoids was studied in cut sprouts of Cannabis sativa by incorporation experiments using mixtures of unlabeled glucose and [1‐ 13 C]glucose or [U‐ 13 C 6 ]glucose. 13 C‐labeling patterns of cannabichromenic acid and tetrahydrocannabinolic acid were analyzed by quantitative NMR spectroscopy. 13 C enrichments and coupling patterns show that the C 10 ‐terpenoid moiety is biosynthesized entirely or predominantly (> 98%) via the recently discovered deoxyxylulose phosphate pathway. The phenolic moiety is generated by a polyketide‐type reaction sequence. The data support geranyl diphosphate and the polyketide, olivetolic acid, as specific intermediates in the biosynthesis of cannabinoids.
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