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Sesquiterpenoids from Chinese Agarwood Induced by Artificial Holing
Two new sesquiterpenoids, 3-oxo-7-hydroxylholosericin A (1) and 1,5;8,12-diepoxy-guaia-12-one (2), together with seven known sesquiterpenoids 3–9, were isolated from Chinese agarwood induced by artificial holing originating from Aquilaria sinensis (Lour.) Gilg. Their structures were identified by sp...
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/PMC6273283/ https://www.ncbi.nlm.nih.gov/pubmed/26927047 http://dx.doi.org/10.3390/molecules21030274 |
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author | Li, Wei Liao, Ge Dong, Wen-Hua Kong, Fan-Dong Wang, Pei Wang, Hao Mei, Wen-Li Dai, Hao-Fu |
author_facet | Li, Wei Liao, Ge Dong, Wen-Hua Kong, Fan-Dong Wang, Pei Wang, Hao Mei, Wen-Li Dai, Hao-Fu |
author_sort | Li, Wei |
collection | PubMed |
description | Two new sesquiterpenoids, 3-oxo-7-hydroxylholosericin A (1) and 1,5;8,12-diepoxy-guaia-12-one (2), together with seven known sesquiterpenoids 3–9, were isolated from Chinese agarwood induced by artificial holing originating from Aquilaria sinensis (Lour.) Gilg. Their structures were identified by spectroscopic techniques (UV, IR, 1D and 2D NMR) and MS analyses. The absolute configuration of compound 1 was determined by comparison of its measured CD curve with that of calculated data for 1 and ent-1. The NMR data of 3 were reported in this study for the first time. Compounds 1, 2, 4–6, together with the EtOAc extract showed moderate inhibitory activities against acetylcholinesterase, and compounds 4–6, 8 exhibited antibacterial activities against Staphylococcus aureus or Ralstonia solanacearum. |
format | Online Article Text |
id | pubmed-6273283 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62732832018-12-28 Sesquiterpenoids from Chinese Agarwood Induced by Artificial Holing Li, Wei Liao, Ge Dong, Wen-Hua Kong, Fan-Dong Wang, Pei Wang, Hao Mei, Wen-Li Dai, Hao-Fu Molecules Article Two new sesquiterpenoids, 3-oxo-7-hydroxylholosericin A (1) and 1,5;8,12-diepoxy-guaia-12-one (2), together with seven known sesquiterpenoids 3–9, were isolated from Chinese agarwood induced by artificial holing originating from Aquilaria sinensis (Lour.) Gilg. Their structures were identified by spectroscopic techniques (UV, IR, 1D and 2D NMR) and MS analyses. The absolute configuration of compound 1 was determined by comparison of its measured CD curve with that of calculated data for 1 and ent-1. The NMR data of 3 were reported in this study for the first time. Compounds 1, 2, 4–6, together with the EtOAc extract showed moderate inhibitory activities against acetylcholinesterase, and compounds 4–6, 8 exhibited antibacterial activities against Staphylococcus aureus or Ralstonia solanacearum. MDPI 2016-02-26 /pmc/articles/PMC6273283/ /pubmed/26927047 http://dx.doi.org/10.3390/molecules21030274 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 by Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Li, Wei Liao, Ge Dong, Wen-Hua Kong, Fan-Dong Wang, Pei Wang, Hao Mei, Wen-Li Dai, Hao-Fu Sesquiterpenoids from Chinese Agarwood Induced by Artificial Holing |
title | Sesquiterpenoids from Chinese Agarwood Induced by Artificial Holing |
title_full | Sesquiterpenoids from Chinese Agarwood Induced by Artificial Holing |
title_fullStr | Sesquiterpenoids from Chinese Agarwood Induced by Artificial Holing |
title_full_unstemmed | Sesquiterpenoids from Chinese Agarwood Induced by Artificial Holing |
title_short | Sesquiterpenoids from Chinese Agarwood Induced by Artificial Holing |
title_sort | sesquiterpenoids from chinese agarwood induced by artificial holing |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273283/ https://www.ncbi.nlm.nih.gov/pubmed/26927047 http://dx.doi.org/10.3390/molecules21030274 |
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