Journal of Asian Natural Products Research · 2016 · 13 citations · 4 references
Life SciencesBotanyPlant SciencesEthnobotanyPlant BiochemistryStructure-activity RelationshipsMedicinal Plant KnowledgeMedicinal PlantsPlant Natural Product BiosynthesisStructure-activity Relationship AnalysisBioactive Plant CompoundsPharmacological ScreeningPlant-derived Natural ProductsSpectroscopic IdentificationTerpenoid Glycosides
Two new 28-nor-oleanane-type triterpene saponins, oleiferoside U (1), and oleiferoside V (2) were isolated from the 50% EtOH extract of the roots of Camellia oleifera C. Abel. Their structures were elucidated as camellenodiol 3β-O-β-d-galactopyranosyl-(1→2)-β-d-xylopyranosyl-(1→2)-[β-d-galactopyranosyl-(1→3)]-β-d-glucuronopyranoside and camellenodiol 3β-O-β-d-galactopyranosyl-(1→3)-β-d-xylopyranosyl-(1→2)-[β-d-galactopyranosyl-(1→3)]-β-d-glucuronopyranoside. Their chemical structures were established mainly on the basis of integrated spectroscopic techniques. In vitro, cytotoxic activities of the two new triterpene saponins were evaluated against three human tumor cell lines (A549, SMMC-7721, and MCF-7) using the MTT assay. Both of them showed a certain cytotoxic activities toward the tested cell lines and gave IC50 values in the range of 45.04-63.22 μM.
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Nguyễn Thị Phương Thảo, Tran Manh Hung, To Dao Cuong et al. · Bioorganic & Medicinal Chemistry Letters · 2010 · 24 citations