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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...

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Detalles Bibliográficos
Autores principales: Li, Wei, Liao, Ge, Dong, Wen-Hua, Kong, Fan-Dong, Wang, Pei, Wang, Hao, Mei, Wen-Li, Dai, Hao-Fu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
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.
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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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