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Anti-Inflammatory Triterpene Glycosides from the Roots of Ilex dunniana Levl
A new triterpene glycoside ilexdunnoside A (1) and a new sulfated triterpene derivative ilexdunnoside B (2), together with five known analogues 3–7 were isolated from the roots of Ilex dunniana Levl. The structures were established by NMR spectroscopic analysis and acid hydrolysis. Results of an in...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6152231/ https://www.ncbi.nlm.nih.gov/pubmed/28753960 http://dx.doi.org/10.3390/molecules22071206 |
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author | Shi, Yu-Sheng Zhang, Yan Hu, Wen-Zhong Chen, Xi Fu, Xin Lv, Xia Zhang, Li-Hong Zhang, Ning Li, Guang |
author_facet | Shi, Yu-Sheng Zhang, Yan Hu, Wen-Zhong Chen, Xi Fu, Xin Lv, Xia Zhang, Li-Hong Zhang, Ning Li, Guang |
author_sort | Shi, Yu-Sheng |
collection | PubMed |
description | A new triterpene glycoside ilexdunnoside A (1) and a new sulfated triterpene derivative ilexdunnoside B (2), together with five known analogues 3–7 were isolated from the roots of Ilex dunniana Levl. The structures were established by NMR spectroscopic analysis and acid hydrolysis. Results of an in vivo study of the biological activity showed that 75% ethanol and n-butanol extracts of the plant displayed anti-inflammatory activities against ear edema in mice, with inhibition rates of 23.5% and 37.5%, respectively, at a dose of 50 mg/kg. Furthermore, Compounds 1, 2 and 3 exhibited moderate indirect inhibitory effects on lipopolysaccharide-induced NO production in BV2 microglial cells in vitro, with IC(50) values of 11.60, 12.30 and 9.70 μM, respectively. |
format | Online Article Text |
id | pubmed-6152231 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-61522312018-11-13 Anti-Inflammatory Triterpene Glycosides from the Roots of Ilex dunniana Levl Shi, Yu-Sheng Zhang, Yan Hu, Wen-Zhong Chen, Xi Fu, Xin Lv, Xia Zhang, Li-Hong Zhang, Ning Li, Guang Molecules Article A new triterpene glycoside ilexdunnoside A (1) and a new sulfated triterpene derivative ilexdunnoside B (2), together with five known analogues 3–7 were isolated from the roots of Ilex dunniana Levl. The structures were established by NMR spectroscopic analysis and acid hydrolysis. Results of an in vivo study of the biological activity showed that 75% ethanol and n-butanol extracts of the plant displayed anti-inflammatory activities against ear edema in mice, with inhibition rates of 23.5% and 37.5%, respectively, at a dose of 50 mg/kg. Furthermore, Compounds 1, 2 and 3 exhibited moderate indirect inhibitory effects on lipopolysaccharide-induced NO production in BV2 microglial cells in vitro, with IC(50) values of 11.60, 12.30 and 9.70 μM, respectively. MDPI 2017-07-19 /pmc/articles/PMC6152231/ /pubmed/28753960 http://dx.doi.org/10.3390/molecules22071206 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Shi, Yu-Sheng Zhang, Yan Hu, Wen-Zhong Chen, Xi Fu, Xin Lv, Xia Zhang, Li-Hong Zhang, Ning Li, Guang Anti-Inflammatory Triterpene Glycosides from the Roots of Ilex dunniana Levl |
title | Anti-Inflammatory Triterpene Glycosides from the Roots of Ilex dunniana Levl |
title_full | Anti-Inflammatory Triterpene Glycosides from the Roots of Ilex dunniana Levl |
title_fullStr | Anti-Inflammatory Triterpene Glycosides from the Roots of Ilex dunniana Levl |
title_full_unstemmed | Anti-Inflammatory Triterpene Glycosides from the Roots of Ilex dunniana Levl |
title_short | Anti-Inflammatory Triterpene Glycosides from the Roots of Ilex dunniana Levl |
title_sort | anti-inflammatory triterpene glycosides from the roots of ilex dunniana levl |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6152231/ https://www.ncbi.nlm.nih.gov/pubmed/28753960 http://dx.doi.org/10.3390/molecules22071206 |
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