Molecules · 2008 · 45 citations · 12 references
PharmacyMedicinal ChemistryPharmacologyDrug DiscoveryPlant BiochemistryStructure-activity RelationshipsMedicinal Plant KnowledgeMedicinal PlantsPhenolic Compound AnalysisStructure-activity Relationship AnalysisActive Compound IsolationBioactive Plant CompoundsFlavonoid GlycosidesIn-vitro CharacterizationPharmacological ScreeningPhenolic CompoundsPhytochemical CompositionPlant Phenolics
A bioassay-guided in vitro screen has revealed that a 70% methanol extract of the leaves of Salix matsudana shows considerable inhibitory activity against cyclooxygenases (COX-1 and COX-2). A subsequent phytochemical study led to the isolation of a new flavonoid, matsudone A (1), together with five known flavonoids--luteolin (2), isoquercitrin (3), 7-methoxyflavone (4), luteolin 7-O-glucoside (5), 4',7-dihydroxyflavone (6)--and two phenolic glycosides, leonuriside A (7) and piceoside (8). Their structures were elucidated on the basis of extensive 1D- and 2D-NMR studies, high resolution ESI mass spectroscopic analyses and comparisons with literature data. The isolated compounds 1-8 were tested for their inhibitory activities against COX-1 and COX-2. Compounds 1, 5 and 6 were found to have potent inhibitory effect on COX-2 and compounds 3-5 exhibited moderate inhibition against COX-1.
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Phenolic compounds from Coix lachryma-jobi var. Ma-yuen
Hideaki Otsuka, Mami Takeuchi, Shogo Inoshiri et al. · Phytochemistry · 1989 · 119 citations
Xanthones from hypericum japonicum and H. henryi
Qingli Wu, Sheng-Ping Wang, Lijun Du et al. · Phytochemistry · 1998 · 80 citations