Antifungal activity of the volatiles of high potency Cannabis sativa L. against Cryptococcus neoformans.
Wanas, A. S., Radwan, M. M., Mehmedic, Z., Jacob, M., Khan, I. A., and Elsohly, M. A. (2016). Rec. Nat. Prod. 10, 214–220.
Abstract: The n-hexane extracted volatile fraction of high potency Cannabis sativa L (Cannabaceae). was assessed in vitro for antifungal, antibacterial and antileishmanial activities. The oil exhibited selective albeit modest, antifungal activity against Cryptococcus neoformans with an IC50 value of 33.1 μg/mL. Biologically- guided fractionation of the volatile fraction resulted in the isolation of three major compounds (1-3) using various chromatographic techniques. The chemical structures of the isolated compounds were identified as α- humulene (1), -caryophyllene (2) and caryophyllene oxide (3) using GC/FID, GC/MS, 1D- and 2D-NMR analyses, respectively. Compound 1 showed potent and selective antifungal activity against Cryptococcus neoformans with IC50 and MIC values of 1.18 g/mL and 5.0 g/mL respectively. Whereas compound 2 showed weak activity (IC50 19.4 μg/mL), while compound 3 was inactive against C. neoformans.
Wanas, A. S., Radwan, M. M., Mehmedic, Z., Jacob, M., Khan, I. A., and Elsohly, M. A. (2016). Rec. Nat. Prod. 10, 214–220.
Abstract: The n-hexane extracted volatile fraction of high potency Cannabis sativa L (Cannabaceae). was assessed in vitro for antifungal, antibacterial and antileishmanial activities. The oil exhibited selective albeit modest, antifungal activity against Cryptococcus neoformans with an IC50 value of 33.1 μg/mL. Biologically- guided fractionation of the volatile fraction resulted in the isolation of three major compounds (1-3) using various chromatographic techniques. The chemical structures of the isolated compounds were identified as α- humulene (1), -caryophyllene (2) and caryophyllene oxide (3) using GC/FID, GC/MS, 1D- and 2D-NMR analyses, respectively. Compound 1 showed potent and selective antifungal activity against Cryptococcus neoformans with IC50 and MIC values of 1.18 g/mL and 5.0 g/mL respectively. Whereas compound 2 showed weak activity (IC50 19.4 μg/mL), while compound 3 was inactive against C. neoformans.