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New Sesquiterpenenoids from Ainsliaea yunnanensis
Investigation of the ethanol extract of the whole plant of Ainsliaea yunnanensis led to the isolation of four new dimeric sesquiterpene lactones, ainsliadimer F–I (1–4), together with seven known dimeric sesquiterpene lactones (5–11) and ten sesquiterpenes (12–21). Their structures were elucidated b...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273759/ https://www.ncbi.nlm.nih.gov/pubmed/27509491 http://dx.doi.org/10.3390/molecules21081031 |
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author | Wu, Xiang-Lei Xiong, Xiao-Juan Lu, Wen-Quan Huang, Hao Shen, Yun-Heng Wu, Zhi-Jun Chen, Wan-Sheng |
author_facet | Wu, Xiang-Lei Xiong, Xiao-Juan Lu, Wen-Quan Huang, Hao Shen, Yun-Heng Wu, Zhi-Jun Chen, Wan-Sheng |
author_sort | Wu, Xiang-Lei |
collection | PubMed |
description | Investigation of the ethanol extract of the whole plant of Ainsliaea yunnanensis led to the isolation of four new dimeric sesquiterpene lactones, ainsliadimer F–I (1–4), together with seven known dimeric sesquiterpene lactones (5–11) and ten sesquiterpenes (12–21). Their structures were elucidated by spectroscopic methods. The relative stereochemistry of ainsliadimer F was further confirmed by single crystal X-ray diffraction analysis. Compounds 1–21 were tested for the inhibition of nuclear factor kappa B (NF-κB) in the 293-NF-κB-luciferase reporter cell line induced by lipopolysaccharide (LPS), and Compounds 5, 18, 20 and 21 were further tested for the production of TNF-α, IL-1β, IL-6 and IL-10 in RAW 264.7 macrophages induced by LPS. Compounds 5, 18, 20 and 21 exhibited significant activity in anti-inflammatory activity assays. |
format | Online Article Text |
id | pubmed-6273759 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62737592018-12-28 New Sesquiterpenenoids from Ainsliaea yunnanensis Wu, Xiang-Lei Xiong, Xiao-Juan Lu, Wen-Quan Huang, Hao Shen, Yun-Heng Wu, Zhi-Jun Chen, Wan-Sheng Molecules Article Investigation of the ethanol extract of the whole plant of Ainsliaea yunnanensis led to the isolation of four new dimeric sesquiterpene lactones, ainsliadimer F–I (1–4), together with seven known dimeric sesquiterpene lactones (5–11) and ten sesquiterpenes (12–21). Their structures were elucidated by spectroscopic methods. The relative stereochemistry of ainsliadimer F was further confirmed by single crystal X-ray diffraction analysis. Compounds 1–21 were tested for the inhibition of nuclear factor kappa B (NF-κB) in the 293-NF-κB-luciferase reporter cell line induced by lipopolysaccharide (LPS), and Compounds 5, 18, 20 and 21 were further tested for the production of TNF-α, IL-1β, IL-6 and IL-10 in RAW 264.7 macrophages induced by LPS. Compounds 5, 18, 20 and 21 exhibited significant activity in anti-inflammatory activity assays. MDPI 2016-08-08 /pmc/articles/PMC6273759/ /pubmed/27509491 http://dx.doi.org/10.3390/molecules21081031 Text en © 2016 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 Wu, Xiang-Lei Xiong, Xiao-Juan Lu, Wen-Quan Huang, Hao Shen, Yun-Heng Wu, Zhi-Jun Chen, Wan-Sheng New Sesquiterpenenoids from Ainsliaea yunnanensis |
title | New Sesquiterpenenoids from Ainsliaea yunnanensis |
title_full | New Sesquiterpenenoids from Ainsliaea yunnanensis |
title_fullStr | New Sesquiterpenenoids from Ainsliaea yunnanensis |
title_full_unstemmed | New Sesquiterpenenoids from Ainsliaea yunnanensis |
title_short | New Sesquiterpenenoids from Ainsliaea yunnanensis |
title_sort | new sesquiterpenenoids from ainsliaea yunnanensis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273759/ https://www.ncbi.nlm.nih.gov/pubmed/27509491 http://dx.doi.org/10.3390/molecules21081031 |
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