Chemical and Pharmaceutical Bulletin · 1997 · 30 citations · 0 references
PharmacyBotanyPlant SciencesCarbohydrate ChemistryNatural Product BiosynthesisPlant BiochemistryPlant Natural Product BiosynthesisTerpenoid BiosynthesisActive Compound IsolationFlavonoid GlycosidesPhenylpropanoid GlycosidesPlant-derived Natural ProductsSaponin BiosynthesisSpectroscopic IdentificationTerpenoid Glycosides
A highly polar saponin mixture from pods of Acacia concinna (Leguminosae) was hydrolyzed with alkali to yield five new triterpenoidal prosapogenols named concinnosides A (6), B (3), C (7), D (4), and E (8), together with four known glycosides, acaciaside, (2), julibroside A1 (10) julibroside A3 (9), albiziasaponin C (5), and their aglycone, acacic acid lactone (1). The structures of these new prosapogenols were elucidated based on spectroscopic means. A less polar saponin fraction from the pods gave spinasteryl glucoside and its dihydro derivative.