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Two New Guaiane Sesquiterpenoids from Daphne holosericea (Diels) Hamaya
Two new sesquiterpenoids with guaiane skeletons—holosericin A (1) and holosericin B (2)—were isolated from the medicinal plant Daphne holosericea (Diels) Hamawa (Thymelaeceae). Their structures were elucidated by 1D and 2D-NMR spectroscopy, as well as HR-ESI-MS data. Compounds 1 and 2 were evaluated...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271883/ https://www.ncbi.nlm.nih.gov/pubmed/25215585 http://dx.doi.org/10.3390/molecules190914266 |
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author | Ma, Qing-Yun Chen, Yi-Chun Huang, Sheng-Zhuo Guo, Zhi-Kai Dai, Hao-Fu Hua, Yan Zhao, You-Xing |
author_facet | Ma, Qing-Yun Chen, Yi-Chun Huang, Sheng-Zhuo Guo, Zhi-Kai Dai, Hao-Fu Hua, Yan Zhao, You-Xing |
author_sort | Ma, Qing-Yun |
collection | PubMed |
description | Two new sesquiterpenoids with guaiane skeletons—holosericin A (1) and holosericin B (2)—were isolated from the medicinal plant Daphne holosericea (Diels) Hamawa (Thymelaeceae). Their structures were elucidated by 1D and 2D-NMR spectroscopy, as well as HR-ESI-MS data. Compounds 1 and 2 were evaluated for inhibitory activities against acetylcholinesterase and compound 2 showed a moderate activity with 31% inhibition. |
format | Online Article Text |
id | pubmed-6271883 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62718832018-12-27 Two New Guaiane Sesquiterpenoids from Daphne holosericea (Diels) Hamaya Ma, Qing-Yun Chen, Yi-Chun Huang, Sheng-Zhuo Guo, Zhi-Kai Dai, Hao-Fu Hua, Yan Zhao, You-Xing Molecules Article Two new sesquiterpenoids with guaiane skeletons—holosericin A (1) and holosericin B (2)—were isolated from the medicinal plant Daphne holosericea (Diels) Hamawa (Thymelaeceae). Their structures were elucidated by 1D and 2D-NMR spectroscopy, as well as HR-ESI-MS data. Compounds 1 and 2 were evaluated for inhibitory activities against acetylcholinesterase and compound 2 showed a moderate activity with 31% inhibition. MDPI 2014-09-11 /pmc/articles/PMC6271883/ /pubmed/25215585 http://dx.doi.org/10.3390/molecules190914266 Text en © 2014 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 license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Ma, Qing-Yun Chen, Yi-Chun Huang, Sheng-Zhuo Guo, Zhi-Kai Dai, Hao-Fu Hua, Yan Zhao, You-Xing Two New Guaiane Sesquiterpenoids from Daphne holosericea (Diels) Hamaya |
title | Two New Guaiane Sesquiterpenoids from Daphne holosericea (Diels) Hamaya |
title_full | Two New Guaiane Sesquiterpenoids from Daphne holosericea (Diels) Hamaya |
title_fullStr | Two New Guaiane Sesquiterpenoids from Daphne holosericea (Diels) Hamaya |
title_full_unstemmed | Two New Guaiane Sesquiterpenoids from Daphne holosericea (Diels) Hamaya |
title_short | Two New Guaiane Sesquiterpenoids from Daphne holosericea (Diels) Hamaya |
title_sort | two new guaiane sesquiterpenoids from daphne holosericea (diels) hamaya |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271883/ https://www.ncbi.nlm.nih.gov/pubmed/25215585 http://dx.doi.org/10.3390/molecules190914266 |
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