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Aldose reductase inhibition by luteolin derivatives from Parasenecio pseudotaimingasaAldose Reductase Inhibition by Luteolin Derivatives from Parasenecio pseudotaimingasa

Authors
Kim, H.M.Lee, J.M.Lee, K.H.Ahn, Y.H.Lee, S.
Issue Date
Dec-2011
Publisher
한국생약학회
Keywords
Luteolin-7-o-glucoside; Luteolin-7-O-rutinoside; Parasenecio pseudotaimingasa; Senecioneae
Citation
Natural Product Sciences, v.17, no.4, pp 367 - 371
Pages
5
Journal Title
Natural Product Sciences
Volume
17
Number
4
Start Page
367
End Page
371
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/21936
ISSN
1226-3907
Abstract
Effects of the extract and fractions from Parasenecio pseudotaimingasa on rat lens aldose reductase (AR) inhibition have been investigated. Among them, the n-BuOH fraction was exhibited good inhibitory potencies (IC 50 value 1.42 μg/ml). Phytochemical constituents were isolated from the n-BuOH fraction by open column chromatography. Their structures were elucidated as luteolin-7-O-rutinoside (1) and luteolin-7-Oglucoside (2) on the basis of spectroscopic analysis. Compounds 1 and 2 exhibited strong AR inhibitory activity, with IC 50 values of 2.37 and 1.05 μM, respectively. This is the first report on the isolation of compounds 1 and 2 from P. pseudotaimingasa. These results suggest that P. pseudotaimingasa could be a useful material in the development of a novel AR inhibitory agent against diabetic complications.
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