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image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Chemistry & Biodiver...arrow_drop_down
image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao
Chemistry & Biodiversity
Article . 2008 . Peer-reviewed
License: Wiley Online Library User Agreement
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Aldose‐Reductase‐ and Protein‐Glycation‐Inhibitory Principles from the Whole Plant ofDuchesnea chrysantha

Authors: Jong Min, Kim; Dae Sik, Jang; Yun Mi, Lee; Jeong Lim, Yoo; Young Sook, Kim; Joo-Hwan, Kim; Jin Sook, Kim;

Aldose‐Reductase‐ and Protein‐Glycation‐Inhibitory Principles from the Whole Plant ofDuchesnea chrysantha

Abstract

AbstractEllagic acid (1), 3,3′‐di‐O‐methylellagic acid (2), 3,3′,4‐tri‐O‐methylellagic acid (3), isovitexin (4), kaempferol 3‐O‐β‐D‐glucuronide methyl ester (5), quercetin 3‐O‐α‐L‐arabinopyranosyl‐(1→6)‐β‐D‐galactopyranoside (6), ursolic acid, pomolic acid, tormentic acid, euscaphic acid, euscaphic acid 28‐O‐β‐D‐glucopyranoside, and maslinic acid were isolated from the AcOEt‐ and BuOH‐soluble MeOH extract ofDuchesnea chrysantha(whole plant). The isolates were subjected toin vitrobioassays to evaluate their inhibitory activity on rat‐lens aldose reductase (RLAR) and formation of advanced glycation end products (AGEs). The ellagic acids and flavonoids, compounds1–6, exhibited moderate inhibitory effects on RLAR. However, compounds1and4–6showed excellent inhibitory activities towards the formation of AGEs. This is the first report that4and6exhibit inhibitory activity towards AR and AGEs formation.

Related Organizations
Keywords

Glycation End Products, Advanced, Molecular Structure, Stereoisomerism, Triterpenes, Rats, Rats, Sprague-Dawley, Structure-Activity Relationship, Ellagic Acid, Aldehyde Reductase, Lens, Crystalline, Ursolic Acid, Animals, Quercetin, Glycosides, Apigenin, Oleanolic Acid, Rosaceae

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
24
Top 10%
Average
Average
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