Natural Product Research · 2012 · 18 citations · 10 references
PharmacyBiochemistryMedicinal ChemistryCancer PharmacologyDrug DiscoveryStructure-activity RelationshipsMedicinal PlantsNatural Product Drug DiscoverySteroid StructureStructure-activity Relationship AnalysisBioactive Plant CompoundsChemical DegradationChemical Degradation PathwaysCytotoxicity AssaysExtractPharmacological ScreeningPhytochemical Composition
A phytochemical investigation of the EtOH extract from the rhizomes and roots of Smilax scobinicaulis resulted in the isolation of a new isospirostanol-type steroidal saponin, namely (25 R)-5α-spirostan-3β,6β-diol 3-O-β-D-glucopyranosyl-(1 → 4)-[α-L-arabinopyranosyl-(1 → 6)]-β-D-glucopyranoside (1), along with four known steroidal saponins (2-5). The structures of these compounds were determined by 1D- and 2D-NMR spectroscopic analysis, FABMS and HR-ESI-MS as well as chemical degradation. The isolated saponins were evaluated for their in vitro cytotoxicity against A549, LAC and Hela human cancer cell lines, which demonstrated that only compound 1 possessed significant cytotoxic activity with IC₅₀ values of 3.70, 5.70 and 3.64 µM, respectively.
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Steroidal saponins from Asparagus africanus*1
Asfaw Debella, Ernst Haslinger, Olaf Kunert et al. · Phytochemistry · 1999 · 66 citations
Steroidal saponins from the rhizomes of Smilax sieboldii
Tamotsu Nikaido, Taichi Ohmoto, Satoshi Kubo et al. · Phytochemistry · 1992 · 48 citations