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Eudesmane-Type Sesquiterpene Glycosides from Dictamnus dasycarpus Turcz.
Eudesmane-type sesquiterpenes have been reported to exhibit varieties of biological activities. During the process of investigating this kind of natural product from the root bark of Dictamnus dasycarpus Turcz., 13 eudesmane-type sesquiterpene glycosides including six new isolates, named as dictameu...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6017781/ https://www.ncbi.nlm.nih.gov/pubmed/29533968 http://dx.doi.org/10.3390/molecules23030642 |
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author | Yang, Shengcai Li, Zheng Wang, Jianli Ruan, Jingya Zheng, Chang Huang, Peijian Han, Lifeng Zhang, Yi Wang, Tao |
author_facet | Yang, Shengcai Li, Zheng Wang, Jianli Ruan, Jingya Zheng, Chang Huang, Peijian Han, Lifeng Zhang, Yi Wang, Tao |
author_sort | Yang, Shengcai |
collection | PubMed |
description | Eudesmane-type sesquiterpenes have been reported to exhibit varieties of biological activities. During the process of investigating this kind of natural product from the root bark of Dictamnus dasycarpus Turcz., 13 eudesmane-type sesquiterpene glycosides including six new isolates, named as dictameudesmnosides A(1) (1), A(2) (2), B (3), C (4), D (5), and E (6), together with seven known ones (7–13), were obtained. Herein, their structures were determined by the analysis of physical data, spectroscopic analysis, and chemical methods. The existence of α-configuration glucose units in their structures (1–5, 8) is not very common in natural glycosidic components. Meanwhile, compounds 3–5, 7, and 9–13 displayed TG accumulation inhibitory effects on HepG2 cells. |
format | Online Article Text |
id | pubmed-6017781 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-60177812018-11-13 Eudesmane-Type Sesquiterpene Glycosides from Dictamnus dasycarpus Turcz. Yang, Shengcai Li, Zheng Wang, Jianli Ruan, Jingya Zheng, Chang Huang, Peijian Han, Lifeng Zhang, Yi Wang, Tao Molecules Article Eudesmane-type sesquiterpenes have been reported to exhibit varieties of biological activities. During the process of investigating this kind of natural product from the root bark of Dictamnus dasycarpus Turcz., 13 eudesmane-type sesquiterpene glycosides including six new isolates, named as dictameudesmnosides A(1) (1), A(2) (2), B (3), C (4), D (5), and E (6), together with seven known ones (7–13), were obtained. Herein, their structures were determined by the analysis of physical data, spectroscopic analysis, and chemical methods. The existence of α-configuration glucose units in their structures (1–5, 8) is not very common in natural glycosidic components. Meanwhile, compounds 3–5, 7, and 9–13 displayed TG accumulation inhibitory effects on HepG2 cells. MDPI 2018-03-13 /pmc/articles/PMC6017781/ /pubmed/29533968 http://dx.doi.org/10.3390/molecules23030642 Text en © 2018 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 Yang, Shengcai Li, Zheng Wang, Jianli Ruan, Jingya Zheng, Chang Huang, Peijian Han, Lifeng Zhang, Yi Wang, Tao Eudesmane-Type Sesquiterpene Glycosides from Dictamnus dasycarpus Turcz. |
title | Eudesmane-Type Sesquiterpene Glycosides from Dictamnus dasycarpus Turcz. |
title_full | Eudesmane-Type Sesquiterpene Glycosides from Dictamnus dasycarpus Turcz. |
title_fullStr | Eudesmane-Type Sesquiterpene Glycosides from Dictamnus dasycarpus Turcz. |
title_full_unstemmed | Eudesmane-Type Sesquiterpene Glycosides from Dictamnus dasycarpus Turcz. |
title_short | Eudesmane-Type Sesquiterpene Glycosides from Dictamnus dasycarpus Turcz. |
title_sort | eudesmane-type sesquiterpene glycosides from dictamnus dasycarpus turcz. |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6017781/ https://www.ncbi.nlm.nih.gov/pubmed/29533968 http://dx.doi.org/10.3390/molecules23030642 |
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