Chemistry & Biodiversity · 2011 · 10 citations · 13 references
PharmacyBiochemistryMedicinal ChemistryCarbohydrate ChemistryDrug DiscoveryStructure-activity RelationshipsGlycan BiosynthesisGlycan StructureStructure-activity Relationship AnalysisAntifeedant ActivityAntifeedant DiscoveryGlycopyranose StructureGlycoside ProfilingPhenylpropanoid GlycosidesTerpenoid Glycosides
Three new pregnane glycosides, 3-O-β-D-glucopyranosyl-(1→2)-α-L-arabinopyranosyl-(20R)-pregn-5-ene-3β,20-diol (1), 3-O-α-L-arabinopyranosyl-(20R)-pregn-5-ene-3β,20-diol-20-O-β-D-glucopyranoside (2), 3-O-α-L-arabinopyranosyl-(20R)-pregn-5-ene-3β,20-diol-20-O-β-D-glucopyranosyl-(1→2)-β-D-glucopyranoside (3) were isolated along with four known compounds, 4-7, from the leaves and stems of Brucea javanica. Their structures were determined by detailed analyses of 1D- and 2D-NMR spectroscopic data. All of the compounds isolated from Brucea javanica were tested for the antifeedant activities against the larva of Pieris rapae. Compounds 1, 3, and 5 showed significant antifeedant activities after 72 h incubation.
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Carbon-13 NMR studies of flavonoids—III
K. R. Markham, B. Ternai, Roger Stanley et al. · Tetrahedron · 1978 · 876 citations