In the endeavor to obtain new antitrypanosomal agents, particularly sesquiterpene lactones, from Kenyan plants of the family Asteraceae, Sch. Bip. was investigated. Bioactivity-guided fractionation and isolation in conjunction with LC/MS-based dereplication has led to the identification of vernodalol () and isolation of vernodalin (), 11β,13-dihydrovernodalin (), 11β,13-dihydrovernolide (), vernolide (), 11β,13-dihydrohydroxyvernolide (), hydroxyvernolide (), and a new germacrolide type sesquiterpene lactone vernocinerascolide () from the dichloromethane extract of leaves. Compounds - were characterized by extensive analysis of their 1D and 2D NMR spectroscopic and HR/MS spectrometric data. All the compounds were evaluated for their in vitro biological activity against bloodstream forms of and for cytotoxicity against the mammalian cell line L6. Vernodalin () was the most active compound with an IC value of 0.16 µM and a selectivity index of 35. Its closely related congener 11β,13-dihydrovernodalin () registered an IC value of 1.1 µM and a selectivity index of 4.2.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6017816 | PMC |
http://dx.doi.org/10.3390/molecules23020248 | DOI Listing |
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