番荔枝科
植物化学
豆甾醇
化学
生物碱
立体化学
抗真菌
核磁共振波谱
传统医学
生物
植物
微生物学
色谱法
生物化学
医学
作者
Maurice Taboula Kayo,Marguérite Kamdem Simo,Maurice Tagatsing Fotsing,Emmanuel Talla,Sophie Laurent,Luce Vander Elst,Céline Henoumont,Emmanuel Yankep,Alfred Ngenge Tamfu,Rodrigue Keumoe,Alex de Théodore Atchade,Elisabeth Zeuko’o Menkem,Modeste Lambert Sameza,Alain Roch,Robert N. Müller,Fabrice Fekam Boyom,Joseph Tanyi Mbafor
标识
DOI:10.1080/14786419.2020.1828409
摘要
Phytochemical study of Uvaria comperei afforded an alkaloid, 8,9-dimethoxy-5H-phenanthridin-6-one (1), isolated and characterised (assignment of 1H and 13C NMR) for the first time from a natural source along with two flavonoids, (2S)-5-hydroxy-7,8-dimethoxyflavanone (2) and (2S)-7-hydroxy-5-methoxy-6,8-dimethylflavone (3). Clethric acid (4), oleanoic acid (5), β-sitosterol 3-O-β-D-glucopyranoside (9), β-sitosterol palmitate (6) and a mixture of stigmasterol (7) and β-sitosterol (8) were isolated from Oxyanthus unilocularis. The structures of these compounds were elucidated using modern spectroscopic techniques including1D and 2D Nuclear Magnetic Resonance (NMR) Spectroscopy (1H, 13C, 1H-1H COSY, HSQC, HMBC) and Mass Spectrometry. Some fractions and compounds from Uvaria comperei exhibited good antifungal activity against clinical isolates and standard strains of yeast species of Candida and Cryptococcus genera while extracts from Oxyanthus unilocularis displayed weak antifungal activity. The results obtained show that Uvaria comperei could be a potential source of antifungal drugs.
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