Journal of Natural Products · 1998 · 29 citations · 8 references
PharmacyBiochemistryMedicinal ChemistryNatural Product BiosynthesisPolysaccharide PropertiesPolysaccharide StructureTerpenoid BiosynthesisFlavonoid GlycosidesGranulocyte ResponsesPhagocytosis ModulationSaponin BiosynthesisTerpene CompoundsTerpenoid Glycosides
A new acylated triterpene-saponin (1), together with a mixture of the known jenisseensosides C and D, has been isolated from the roots of Silene fortunei. The structure of the new compound was established by chemical means and spectroscopic methods as 3-O-[beta-D-galactopyranosyl-(1-->2)-beta-D-glucuronopyranosyl]-28 -O- [[alpha-L-arabinopyranosyl-(1-->2)-alpha-L-arabinopyranosyl- (1-->3)-b eta-D-xylopyranosyl-(1-->4)-alpha-L-rhamnopyranosyl-(1-->2)]-[beta-D- glucopyranosyl-(1-->3)]-4-O-acetyl-beta-D-fucopyranosyl]quillaic acid. This saponin showed a significant enhancement of granulocyte phagocytosis in vitro.
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Four triterpenoid saponins from dried roots of Gypsophila species
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Pharmacy, Biochemistry, Chemistry +13
Acylated triterpene saponins from Silene jenisseensis
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