A novel nor-megastigmane, normegastigmane-5,9-epoxy-3,8-diol (), together with 10 known compounds of diverse classes including megastigmanes, sesquiterpenoids, and triterpenoids were isolated from the leaves of . The structure of was established by 1D and 2D NMR and HRESIMS data analysis. The known compounds were identified as 5,11-epoxy-3,9-megastigmanediol (), 7-megastigmene-3,6,9-triol (), 1,3-dihydroxypropan-2-yl stearate (), (1,5)-1,5-dimethyl-8-(propan-2-ylidene)cyclodeca-1,5-diene germacrene () 3,5-dihyroxy-6,7-megastigmadien-9-one (), squalene (), -amyrin (), -amyrone (), -amyrin eicosanoate (), and -sitosterol ().
View Article and Find Full Text PDFPhytochemical investigation of the leaves and bark of has led to the isolation of six new iridoids, subcordatanols I-V (- and ) and 1--methylcrescentin I (), along with two known analogues ( and ). Among them, subcordatanol I () is the first example of a 3,8-monoepoxy-iridoid featuring a caged 2-oxa-bicyclo[3.2.
View Article and Find Full Text PDFContext: Plants harbor endophytes with potential bioactivity. Markhamia tomentosa (Benth) K. Schum ex.
View Article and Find Full Text PDFEthnopharmacological Relevance: Markhamia tomentosa (Benth.) K. Schum Ex Engl.
View Article and Find Full Text PDFNatural product compounds obtained from medicinal plants have been great contributions in the discovery of numerous clinically useful drugs. Markhamia species have been reportedly used by many cultures in human and veterinary traditional medicines. The five identified species of Markhamia, that is, Markhamia lutea, Markhamia obtusifolia, Markhamia stipulata, Markhamia tomentosa, and Markhamia zanzibarica have been the subject of chemical investigations that have led to the characterization of their secondary metabolites.
View Article and Find Full Text PDFEthnopharmacological Relevance: Markhamia tomentosa (Benth) K. Schum ex. Engl.
View Article and Find Full Text PDFThis study investigates the antioxidant and antibacterial activities of aqueous and methanolic extracts from Hymenocardia acida Tul. (Hymenocardiaceae). The inhibition values of the extracts and quercetin were found to be very close, with no significant differences at a concentration of 0.
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