<em>α</em>-Glucosidase Inhibitory Constituents from <em>Acanthopanax senticosus</em> Harm Leaves

A new triterpene glycoside, 3-<em>O</em>-[(<em>α</em>-L-rhamnopyranosyl)(1→2)]-[<em>β</em>-D-glucuronopyranosyl-6-<em>O</em>-methyl ester]-olean-12-ene-28-olic acid (<strong>...

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Main Authors: Hai-Xue Kuang, Yong-Gang Xia, Hai Jiang, Zhi-Bin Wang, Bing-You Yang
Format: Article
Language:English
Published: MDPI AG 2012-05-01
Series:Molecules
Subjects:
Online Access:http://www.mdpi.com/1420-3049/17/6/6269
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spelling doaj-0575d35d1b534bf599dd3fe87bd555f52020-11-24T23:05:19ZengMDPI AGMolecules1420-30492012-05-011766269627610.3390/molecules17066269<em>α</em>-Glucosidase Inhibitory Constituents from <em>Acanthopanax senticosus</em> Harm LeavesHai-Xue KuangYong-Gang XiaHai JiangZhi-Bin WangBing-You YangA new triterpene glycoside, 3-<em>O</em>-[(<em>α</em>-L-rhamnopyranosyl)(1→2)]-[<em>β</em>-D-glucuronopyranosyl-6-<em>O</em>-methyl ester]-olean-12-ene-28-olic acid (<strong>1</strong>) and a new indole alkaloid, 5-methoxy-2-oxoindolin-3-acetic acid methyl ester (<strong>5</strong>) were isolated from the leaves of <em>Acanthopanax senticosus</em> Harms along with six known compounds. The structures of the new compounds were determined by means of 2D-NMR experiments and chemical methods. All the isolated compounds were evaluated for their glycosidase inhibition activities and compound <strong>6</strong> showed significant <em>α</em>-glucosidase inhibition activity.http://www.mdpi.com/1420-3049/17/6/6269<em>Acanthopanax senticosus</em> Harmstriterpene glycosidealkaloid<em>α</em>-glucosidase inhibition activity
collection DOAJ
language English
format Article
sources DOAJ
author Hai-Xue Kuang
Yong-Gang Xia
Hai Jiang
Zhi-Bin Wang
Bing-You Yang
spellingShingle Hai-Xue Kuang
Yong-Gang Xia
Hai Jiang
Zhi-Bin Wang
Bing-You Yang
<em>α</em>-Glucosidase Inhibitory Constituents from <em>Acanthopanax senticosus</em> Harm Leaves
Molecules
<em>Acanthopanax senticosus</em> Harms
triterpene glycoside
alkaloid
<em>α</em>-glucosidase inhibition activity
author_facet Hai-Xue Kuang
Yong-Gang Xia
Hai Jiang
Zhi-Bin Wang
Bing-You Yang
author_sort Hai-Xue Kuang
title <em>α</em>-Glucosidase Inhibitory Constituents from <em>Acanthopanax senticosus</em> Harm Leaves
title_short <em>α</em>-Glucosidase Inhibitory Constituents from <em>Acanthopanax senticosus</em> Harm Leaves
title_full <em>α</em>-Glucosidase Inhibitory Constituents from <em>Acanthopanax senticosus</em> Harm Leaves
title_fullStr <em>α</em>-Glucosidase Inhibitory Constituents from <em>Acanthopanax senticosus</em> Harm Leaves
title_full_unstemmed <em>α</em>-Glucosidase Inhibitory Constituents from <em>Acanthopanax senticosus</em> Harm Leaves
title_sort <em>α</em>-glucosidase inhibitory constituents from <em>acanthopanax senticosus</em> harm leaves
publisher MDPI AG
series Molecules
issn 1420-3049
publishDate 2012-05-01
description A new triterpene glycoside, 3-<em>O</em>-[(<em>α</em>-L-rhamnopyranosyl)(1→2)]-[<em>β</em>-D-glucuronopyranosyl-6-<em>O</em>-methyl ester]-olean-12-ene-28-olic acid (<strong>1</strong>) and a new indole alkaloid, 5-methoxy-2-oxoindolin-3-acetic acid methyl ester (<strong>5</strong>) were isolated from the leaves of <em>Acanthopanax senticosus</em> Harms along with six known compounds. The structures of the new compounds were determined by means of 2D-NMR experiments and chemical methods. All the isolated compounds were evaluated for their glycosidase inhibition activities and compound <strong>6</strong> showed significant <em>α</em>-glucosidase inhibition activity.
topic <em>Acanthopanax senticosus</em> Harms
triterpene glycoside
alkaloid
<em>α</em>-glucosidase inhibition activity
url http://www.mdpi.com/1420-3049/17/6/6269
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