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Published September 30, 2015 | Version v1
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Minor oxygenated cannabinoids from high potency Cannabis sativa L.

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  • 1. National Center for Natural Products Research, School of Pharmacy, The University of Mississippi, University, MS 38677, United States & -THC, and 1 S-hydroxycannabinol, respectively. The latter compound showed moderate anti-MRSa (IC 10.0 µg/mL), moderate antileishmanial (IC 14.0 µg/mL) and mild antimalarial activity against Plasmodium falciparum (D6 clone) and P. falciparum (W2 clone) with IC values of 3.4 and 2.3 µg/mL, respectively. & Department of Pharmacognosy, Faculty of Pharmacy, Suez Canal University, Ismailia, Egypt

Description

Ahmed, Safwat A., Ross, Samir A., Slade, Desmond, Radwan, Mohamed M., Khan, Ikhlas A., ElSohly, Mahmoud A. (2015): Minor oxygenated cannabinoids from high potency Cannabis sativa L. Phytochemistry 117: 194-199, DOI: 10.1016/j.phytochem.2015.04.007, URL: http://dx.doi.org/10.1016/j.phytochem.2015.04.007

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urn:lsid:plazi.org:pub:FFFDFF8BFFADD6058A7AFF9FDD2EFFBF

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Figure: 10.5281/zenodo.10486063 (DOI)
Figure: 10.5281/zenodo.10486065 (DOI)
Figure: 10.5281/zenodo.10486068 (DOI)

References

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  • Ahmed, S.A., Ross, S.A., Slade, D., Radwan, M.M., Ikhlas, A.K., ElSohly, M.A., 2008b. Structure determination and absolute configuration of cannabichromanone derivatives from high potency Cannabis sativa. Tetrahedron Lett. 49, 6050-6053.
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