Cannabiripsol: A novelCannabis constituent

@article{Boeren2005CannabiripsolAN,
  title={Cannabiripsol: A novelCannabis constituent},
  author={E. G. Boeren and Mahmoud A. Elsohly and Carlton E. Turner},
  journal={Experientia},
  year={2005},
  volume={35},
  pages={1278-1279}
}
Cannabiripsol [(−)(6aR, 9S, 10S, 10aR)9,10-dihydroxy-hexahydrocannabinol] (1), a new cannabinoid was isolated from a South African Cannabis variant. The structure was determined by spectral means and by synthesis. 
8 Citations
Isolation and Pharmacological Evaluation of Minor Cannabinoids from High-Potency Cannabis sativa.
TLDR
Seven new naturally occurring hydroxylated cannabinoids (1-7), along with the known cannabiripsol (8), have been isolated from the aerial parts of high-potency Cannabis sativa and the results indicated that compound 3 exerted the most potent cannabimimetic-like actions in the tetrad assay.
Pitfalls in the analysis of phytocannabinoids in cannabis inflorescence
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The present review outlines all the possible pitfalls that can be encountered during the analysis of these compounds and aims to be a valuable help for the analytical chemist.
Phytocannabinoids: a unified critical inventory.
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The integrated inventory of these compounds and their biological macromolecular end-points highlights the opportunities that phytocannabinoids offer to access desirable drug-like space beyond the one associated to the narcotic target CB1.

References

SHOWING 1-5 OF 5 REFERENCES
(±)9, 10-dihydroxy-Δ 6a(10a)-tetrahydrocanabinol and (±)8, 9-dihydroxy-Δ 6a(10a)-tetrahydrocannabinol: 2 new cannabinoids fromCannabis sativa L.
The structures of 2 new polyhydroxylated cannabinoids, (±)9, 10-dihydroxy-Δ 6a(10a)-tetrahydorcannabinol and (±)8, 9-dihydroxy-Δ 6a(10a)-tetrahydrocannabinol, obtained from a hexane extract of an
Constituents of Cannabis sativa L. VII: use of silyl derivatives in routine analysis.
Naturally occurring cannabinoids previously impossible to separate and analyze were quantitated on a routine basis using silylation. Relative retention times of many silylated cannabinoids are
The use of labelled analogues for the determination of mass spectrometric fragmentation mechanisms of cannabinoids. A re‐investigation of the formation of the most abundant fragment ion [C15,H19,O2]+ in Δ1(6)tetrahydrocannabinol
The routes leading to the formation of the most prominent fragment ion [C15H19O2]+ (m/e 231) in the cannabinoid Δ1(6) tetrahydrocannabinol were investigated with the aid of deuterium labelled