Journal of Natural Products · 2011 · 73 citations · 19 references
PharmacyBotanyPlant SciencesDrug DiscoveryPlant BiochemistryStructure-activity RelationshipsMedicinal Plant KnowledgeMedicinal PlantsPlant Natural Product BiosynthesisStructure-activity Relationship AnalysisActive Compound IsolationBioactive Plant CompoundsEscherichia ColiSaponin BiosynthesisTerpene CompoundsTerpenoid GlycosidesTerpenoid Profiling
Three new bidesmosidic saponins (1-3) and a new ursane triterpenoid, 2α,3β,11α,23-tetrahydroxyurs-12-en-28-oic acid (4), along with seven known compounds, were isolated from a methanolic extract of the leaves of Symplocos lancifolia. The bidesmosidic saponins were found to possess the same sugar unit part, composed of two β-d-glucose moieties and one α-l-rhamnose moiety, linked to maslinic acid, arjunolic acid, and asiatic acid, respectively. Their structures were elucidated by interpretation of their 1D and 2D NMR spectra and completed by analysis of the HRESIMS data. The antibacterial activity of the isolated triterpenoids was evaluated against Staphylococcus aureus, Enterococcus faecalis, Escherichia coli, and Pseudomonas aeruginosa, and several showed activity against Gram-positive bacteria.
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13C nmr study of α- and β-anomeric pairs of d-mannopyranosides and l-rhamnopyranosides
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