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New 18(4→3)-Abeo-Abietanoids from Tripterygium wilfordii
Three 18(4→3)-abeo-abietanoids, a new natural product and two new compounds, named tripordolides A–C (1–3), were isolated from the leaves of Tripterygium wilfordii. Their structures were elucidated on the basis of their spectroscopic analysis, and the absolute configuration of compounds was confirme...
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/PMC6222710/ https://www.ncbi.nlm.nih.gov/pubmed/30261626 http://dx.doi.org/10.3390/molecules23102467 |
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author | Ni, Lin Zang, Ying-da Yang, Jing-zhi Li, Chuang-jun Ma, Jie Zhang, Dong-ming |
author_facet | Ni, Lin Zang, Ying-da Yang, Jing-zhi Li, Chuang-jun Ma, Jie Zhang, Dong-ming |
author_sort | Ni, Lin |
collection | PubMed |
description | Three 18(4→3)-abeo-abietanoids, a new natural product and two new compounds, named tripordolides A–C (1–3), were isolated from the leaves of Tripterygium wilfordii. Their structures were elucidated on the basis of their spectroscopic analysis, and the absolute configuration of compounds was confirmed by CD and X-ray crystallographic analysis using anomalous scattering of Cu Kα radiation. Compounds 1 and 3 showed moderate inhibitory activities against NO production in lipopolysaccharide-induced (LPS) RAW 264.7 macrophages in vitro. |
format | Online Article Text |
id | pubmed-6222710 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62227102018-11-13 New 18(4→3)-Abeo-Abietanoids from Tripterygium wilfordii Ni, Lin Zang, Ying-da Yang, Jing-zhi Li, Chuang-jun Ma, Jie Zhang, Dong-ming Molecules Article Three 18(4→3)-abeo-abietanoids, a new natural product and two new compounds, named tripordolides A–C (1–3), were isolated from the leaves of Tripterygium wilfordii. Their structures were elucidated on the basis of their spectroscopic analysis, and the absolute configuration of compounds was confirmed by CD and X-ray crystallographic analysis using anomalous scattering of Cu Kα radiation. Compounds 1 and 3 showed moderate inhibitory activities against NO production in lipopolysaccharide-induced (LPS) RAW 264.7 macrophages in vitro. MDPI 2018-09-26 /pmc/articles/PMC6222710/ /pubmed/30261626 http://dx.doi.org/10.3390/molecules23102467 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 Ni, Lin Zang, Ying-da Yang, Jing-zhi Li, Chuang-jun Ma, Jie Zhang, Dong-ming New 18(4→3)-Abeo-Abietanoids from Tripterygium wilfordii |
title | New 18(4→3)-Abeo-Abietanoids from Tripterygium wilfordii |
title_full | New 18(4→3)-Abeo-Abietanoids from Tripterygium wilfordii |
title_fullStr | New 18(4→3)-Abeo-Abietanoids from Tripterygium wilfordii |
title_full_unstemmed | New 18(4→3)-Abeo-Abietanoids from Tripterygium wilfordii |
title_short | New 18(4→3)-Abeo-Abietanoids from Tripterygium wilfordii |
title_sort | new 18(4→3)-abeo-abietanoids from tripterygium wilfordii |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6222710/ https://www.ncbi.nlm.nih.gov/pubmed/30261626 http://dx.doi.org/10.3390/molecules23102467 |
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