Abstract
Phytochemical studies on the stem bark of Guibourtia tessmanii yielded a dihydrochalcone glucoside, 2',4-dihydroxy-4'-methoxy-6'-O-beta-glucopyranoside dihydrochalcone and a new stilbene glycoside, 3,5-dimethoxy-4'-O-(beta-rhamnopyranosyl-(1-->6)-beta- glucopyranoside) stilbene besides the known pterostilbene. Their structures were established on the basis of one and two dimensional NMR spectroscopic techniques, FABMS and chemical evidence.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Chalcone / analogs & derivatives
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Chalcone / chemistry
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Chalcone / isolation & purification*
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Chalcones
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Fabaceae / chemistry*
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Molecular Structure
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Phenols / chemistry
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Phenols / isolation & purification*
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Spectrum Analysis
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Stilbenes / chemistry
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Stilbenes / isolation & purification*
Substances
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2',4-dihydroxy-4'-methoxy-6'-O-glucopyranoside dihydrochalcone
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3,5-dimethoxy-4'-O-(rhamnopyranosyl-(1-6)-glucopyranoside) stilbene
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Chalcones
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Phenols
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Stilbenes
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pterostilbene
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Chalcone