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New Triterpene Glucosides from the Roots of Rosa laevigata Michx
Two new ursane-type triterpene glucosides, 2α,3α,24-trihydroxyurs-12,18-dien-28-oic acid β-d-glucopyranosyl ester (1) and 2α,3α,23-trihydroxyurs-12,19(29)-dien-28-oic acid β-d-glucopyranosyl ester (2), were isolated from the roots of Rosa laevigata, together with three known compounds: 2α,3β,19α-tri...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6244960/ https://www.ncbi.nlm.nih.gov/pubmed/18830152 http://dx.doi.org/10.3390/molecules13092229 |
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author | Yuan, Jing-Quan Yang, Xin-Zhou Miao, Jian-Hua Tang, Chun-Ping Ke, Chang-Qiang Zhang, Ji-Bao Ma, Xiao-Jun Ye, Yang |
author_facet | Yuan, Jing-Quan Yang, Xin-Zhou Miao, Jian-Hua Tang, Chun-Ping Ke, Chang-Qiang Zhang, Ji-Bao Ma, Xiao-Jun Ye, Yang |
author_sort | Yuan, Jing-Quan |
collection | PubMed |
description | Two new ursane-type triterpene glucosides, 2α,3α,24-trihydroxyurs-12,18-dien-28-oic acid β-d-glucopyranosyl ester (1) and 2α,3α,23-trihydroxyurs-12,19(29)-dien-28-oic acid β-d-glucopyranosyl ester (2), were isolated from the roots of Rosa laevigata, together with three known compounds: 2α,3β,19α-trihydroxyurs-12-en-28-oic acid β-d-glucopyranosyl ester (3), 2α,3α,19α-trihydroxyurs-12-en-28-oic acid β-d-glucopyranosyl ester (4) and 2α,3β,19α,23-tetrahydroxyurs-12-en-28-oic acid β-d-glucopyranosyl ester (5). The structures of new compounds were established on the basis of detailed 1D and 2D NMR spectroscopic analyses. Compounds 2 and 5 exhibited modest in vitro antifungal activities against Candida albicans and C. krusei. |
format | Online Article Text |
id | pubmed-6244960 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62449602018-11-30 New Triterpene Glucosides from the Roots of Rosa laevigata Michx Yuan, Jing-Quan Yang, Xin-Zhou Miao, Jian-Hua Tang, Chun-Ping Ke, Chang-Qiang Zhang, Ji-Bao Ma, Xiao-Jun Ye, Yang Molecules Article Two new ursane-type triterpene glucosides, 2α,3α,24-trihydroxyurs-12,18-dien-28-oic acid β-d-glucopyranosyl ester (1) and 2α,3α,23-trihydroxyurs-12,19(29)-dien-28-oic acid β-d-glucopyranosyl ester (2), were isolated from the roots of Rosa laevigata, together with three known compounds: 2α,3β,19α-trihydroxyurs-12-en-28-oic acid β-d-glucopyranosyl ester (3), 2α,3α,19α-trihydroxyurs-12-en-28-oic acid β-d-glucopyranosyl ester (4) and 2α,3β,19α,23-tetrahydroxyurs-12-en-28-oic acid β-d-glucopyranosyl ester (5). The structures of new compounds were established on the basis of detailed 1D and 2D NMR spectroscopic analyses. Compounds 2 and 5 exhibited modest in vitro antifungal activities against Candida albicans and C. krusei. MDPI 2008-09-22 /pmc/articles/PMC6244960/ /pubmed/18830152 http://dx.doi.org/10.3390/molecules13092229 Text en © 2008 by the authors. Licensee Molecular Diversity Preservation International, Basel, Switzerland. This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Yuan, Jing-Quan Yang, Xin-Zhou Miao, Jian-Hua Tang, Chun-Ping Ke, Chang-Qiang Zhang, Ji-Bao Ma, Xiao-Jun Ye, Yang New Triterpene Glucosides from the Roots of Rosa laevigata Michx |
title | New Triterpene Glucosides from the Roots of Rosa laevigata Michx |
title_full | New Triterpene Glucosides from the Roots of Rosa laevigata Michx |
title_fullStr | New Triterpene Glucosides from the Roots of Rosa laevigata Michx |
title_full_unstemmed | New Triterpene Glucosides from the Roots of Rosa laevigata Michx |
title_short | New Triterpene Glucosides from the Roots of Rosa laevigata Michx |
title_sort | new triterpene glucosides from the roots of rosa laevigata michx |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6244960/ https://www.ncbi.nlm.nih.gov/pubmed/18830152 http://dx.doi.org/10.3390/molecules13092229 |
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