期刊
JOURNAL OF THE KOREAN SOCIETY FOR APPLIED BIOLOGICAL CHEMISTRY
卷 52, 期 5, 页码 493-497出版社
KOREAN SOC APPLIED BIOLOGICAL CHEMISTRY
DOI: 10.3839/jksabc.2009.084
关键词
diabetic complications; flavonoids; human aldose reductase; inhibitory activity; leaves; Salix hulteni
From the n-BuOH soluble fraction of the leaves of Salix hulteni, six compounds were isolated as aldose reductase inhibitors. On the basis of spectral data, these compounds were identified as diosmetin-7-O-beta-D-glucoside (1), isoquercitrin (2), diosmetin-7-O-beta-D-xylosyl-(1 -> 6)-beta-D-glucoside (3), aromadendrin-3-O-beta-D-glucoside (4), astragalin (5), and p-hydroxyacetophenone glucoside (6). All of the isolates were evaluated in vitro for inhibitory activity against the aldose reductase. Of these, compounds 1-5 exhibited inhibitory activity against aldose reductase with IC50 values ranging 1.4 to 5.8 mu M.
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