Chemical and Pharmaceutical Bulletin · 2003 · 34 citations · 9 references
Life SciencesBiochemistryPlant BiologyNatural Product BiosynthesisPlant BiochemistryStructure-activity RelationshipsGlycan StructureMedicinal PlantsStructure-activity Relationship AnalysisBioactivityBioactivity In Vitro TestingBioactivity ScreeningBioactivity TestingPhenylpropanoid GlycosidesSaponin BiosynthesisTerpenoid GlycosidesTwo-dimensional Nmr Spectroscopy
Two new pregnane glycosides (1, 2) together with two known saponins were isolated from the rhizomes of Dioscorea futschauensis R. KUNTH. The structures of 1 and 2 were established as 16alpha-methoxyl-3beta-[(O-alpha-L-rhamnopyranosyl-(1-->2)-O-[alpha-L-rhamnopyranosyl-(1-->4)]-beta-D-glucopyranosyl)oxy]pregn-5-en-20-one and 21-methoxyl-3beta-[(O-alpha-L-rhamnopyranosyl-(1-->2)-O-[alpha-L-rhamnopyranosyl-(1-->4)]-beta-D-glucopyranosyl)oxy]pregn-5,16-en-20-one, respectively, on the basis of two-dimension NMR (2D NMR) and other spectral analysis. Their in vitro bioactivity against plant pathogenic fungus Pyricularia oryzae and osteoblastic proliferation stimulatory activity in the UMR106 cell line were evaluated.
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A furostanol glycoside from rhizomes of Dioscorea collettii var. hypoglauca
Ke Hu, Aijun Dong, Xin‐Sheng Yao et al. · Phytochemistry · 1997 · 29 citations