Journal of Natural Products · 2003 · 78 citations · 9 references
PharmacyBiochemistryBotanyNatural Product BiosynthesisPlant BiochemistryStructure-activity RelationshipsMedicinal Plant KnowledgeMedicinal PlantsPlant Natural Product BiosynthesisStructure-activity Relationship AnalysisTerpenoid BiosynthesisActive Compound IsolationBioactive Plant CompoundsConcentrationHemolytic Activity TestingImmunomodulatory EffectsPharmacological ScreeningSaponin BiosynthesisTerpenoid Glycosides
Two new oleanane-type triterpene saponins, adianthifoliosides A (1) and B (2), were isolated from a 95% ethanolic extract of roots of Albizia adianthifolia. Their structures were elucidated mainly by using a combination of 600 MHz 1D and 2D NMR techniques (COSY, NOESY, TOCSY, HSQC, and HMBC) and by FABMS and HRESIMS. Compounds 1 and 2 were characterized as glycosides of acacic acid acylated by an o-hydroxybenzoyl unit. The crude saponin mixture (CSM), compounds 1 and 2 together with 3 and 4 (prosapogenins obtained from the mild alkaline hydrolysate of the CSM), were evaluated for immunomodulatory activity on the Jurkat T cell line and for hemolytic property against sheep erythrocytes. Compound 2 and, to a lesser extent, 1 and 3 were found to exhibit a dose-dependent immunomodulatory effect in the concentration range 10(-2)-10 microM, whereas 4 showed a lymphoproliferative activity in the same concentration range. Among the compounds tested, only 1 and 2 were found to be hemolytic.
9
Shuuji Hara, Hikaru Okabe, Kunihide Mihashi · Chemical and Pharmaceutical Bulletin · 1987 · 543 citations · Full text
Analytical profiles of drug substances and excipients
Analytica Chimica Acta · 1997 · 526 citations
Cytotoxic Glycosides from <i>Albizia julibrissin</i>
Tsuyoshi Ikeda, Satoko Fujiwara, Kaoru Araki et al. · Journal of Natural Products · 1997 · 81 citations
Life Sciences, Biochemistry, Botany +16