Published September 30, 2015
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Fig. 3 in Minor oxygenated cannabinoids from high potency Cannabis sativa L.
Authors/Creators
- 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
Fig. 3. Mosher ester analysis of 9.
Notes
Published as part of 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., pp. 194-199 in Phytochemistry 117 on page 198, DOI: 10.1016/j.phytochem.2015.04.007, http://zenodo.org/record/10486061
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- Is part of
- Journal article: 10.1016/j.phytochem.2015.04.007 (DOI)
- Journal article: urn:lsid:plazi.org:pub:FFFDFF8BFFADD6058A7AFF9FDD2EFFBF (LSID)
- Journal article: https://zenodo.org/record/10486061 (URL)