Four new mexicanolide-type limonoids, swietemicrolides A-D (1-4), together with three known compounds (5-7) were isolated from an ethyl acetate extract of the bark of . 1 and 2 had 1,8-hemiacetal systems whilst 3 and 4 shared hexacyclic skeletons consisting of three fused five-membered rings. The structures of the isolated compounds were determined using spectroscopic methods.
View Article and Find Full Text PDFNine compounds including a new one, garcichaudiic acid (), were isolated from the bark of and their structures were characterized mainly by 1 D and 2 D NMR experiments. The antioxidant capacity of the isolated compounds was determined using DPPH radical scavenging assay and the anti-hyperglycemic activity was assessed by measuring the inhibitory effect against α-glucosidase. Among them, compound showed higher antioxidant activity than the positive control, ascorbic acid, while both compounds and exhibited more significant α-glucosidase inhibitory activity than the reference drug acarbose.
View Article and Find Full Text PDFTwo new polyisoprenylated benzophenones, planchoniones A () and B (), together with two known benzophenones () and six known xanthones (), were isolated from an ethyl acetate extract of the pericarp of Pierre. Their structures were established using spectroscopic methods, mainly 1D and 2D NMR. The four benzophenones were evaluated for their cytotoxicity against MCF-7 human breast cancer cells, and showed almost no activity.
View Article and Find Full Text PDFA new xanthone, planchoxanthone (1), together with six known compounds, garcinianone A (2), cowanin (3), rubraxanthone (4), f-mangostin (5), dulcisxanthone B (6), and guttiferone Q (7), were isolated from an n-hexane extract of the pericap of Garcinia planchonii. Their structures were elucidated using spectroscopic methods. Antioxidant activity of the isolated compounds was tested using the DPPH free radical scavenging assay.
View Article and Find Full Text PDF