Abstract
A new isoflavone glycoside, 6-methoxy-7-hydroxy-4'-O-beta-D-glucosyl isoflavone, glycitein-4'-O-beta-D-glucoside (10), along with nine known flavonoids, were isolated from the stem bark of Sophora japonica. The structures of these compounds were determined by analysis of spectroscopic data (1D -, 2D - NMR and HRMS). The inhibitory effects of all the isolated compounds on aldose reductase were evaluated in vitro. Among these compounds, daidzein (1), puerol A (4), and paratensein-7-O-glucoside (9) exhibited potent inhibitory effects, with IC(50) values of 3.2, 6.4, and 1.9 microM, respectively.
MeSH terms
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Aldehyde Reductase / antagonists & inhibitors
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Animals
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Enzyme Inhibitors / administration & dosage
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Enzyme Inhibitors / isolation & purification
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Enzyme Inhibitors / pharmacology
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Flavonoids / administration & dosage
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Flavonoids / isolation & purification
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Flavonoids / pharmacology*
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Glycosides / administration & dosage
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Glycosides / isolation & purification
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Glycosides / pharmacology*
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Isoflavones / administration & dosage
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Isoflavones / isolation & purification
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Isoflavones / pharmacology*
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Lens, Crystalline / enzymology
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Plant Bark
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Rats
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Rats, Sprague-Dawley
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Sophora / chemistry*
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Spectrum Analysis
Substances
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Enzyme Inhibitors
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Flavonoids
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Glycosides
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Isoflavones
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Aldehyde Reductase