Cargando…

UPLC-MS-guided isolation of single ether linkage dimeric 2-(2-phenylethyl)chromones from Aquilaria sinensis

Eleven novel uncommon single ether linkage dimeric 2-(2-phenylethyl)chromones (aquilasinenones A–K) were isolated by a UPLC-MS guided method from artificial hole-induced agarwood originating from Aquilaria sinensis. Their structures were unambiguously deduced using HRESIMS data, detailed 1D and 2D N...

Descripción completa

Detalles Bibliográficos
Autores principales: Kuang, Tongdong, Chen, Hui-Qin, Wang, Hao, Kong, Fan-Dong, Cai, Cai-Hong, Dong, Wen-Hua, Yuan, Jing-Zhe, Mei, Wen-Li, Dai, Hao-Fu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9064565/
https://www.ncbi.nlm.nih.gov/pubmed/35519867
http://dx.doi.org/10.1039/c9ra02597a
_version_ 1784699407307898880
author Kuang, Tongdong
Chen, Hui-Qin
Wang, Hao
Kong, Fan-Dong
Cai, Cai-Hong
Dong, Wen-Hua
Yuan, Jing-Zhe
Mei, Wen-Li
Dai, Hao-Fu
author_facet Kuang, Tongdong
Chen, Hui-Qin
Wang, Hao
Kong, Fan-Dong
Cai, Cai-Hong
Dong, Wen-Hua
Yuan, Jing-Zhe
Mei, Wen-Li
Dai, Hao-Fu
author_sort Kuang, Tongdong
collection PubMed
description Eleven novel uncommon single ether linkage dimeric 2-(2-phenylethyl)chromones (aquilasinenones A–K) were isolated by a UPLC-MS guided method from artificial hole-induced agarwood originating from Aquilaria sinensis. Their structures were unambiguously deduced using HRESIMS data, detailed 1D and 2D NMR spectroscopic analysis, and experimental ECD spectra. All the compounds were tested for acetylcholinesterase (AChE) inhibitory activity by Ellman's colorimetric method, and compounds 9–11 displayed weak AChE inhibitory activity with the inhibition ranging from 15.6% to 16.8% at a concentration of 50 μg mL(−1).
format Online
Article
Text
id pubmed-9064565
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher The Royal Society of Chemistry
record_format MEDLINE/PubMed
spelling pubmed-90645652022-05-04 UPLC-MS-guided isolation of single ether linkage dimeric 2-(2-phenylethyl)chromones from Aquilaria sinensis Kuang, Tongdong Chen, Hui-Qin Wang, Hao Kong, Fan-Dong Cai, Cai-Hong Dong, Wen-Hua Yuan, Jing-Zhe Mei, Wen-Li Dai, Hao-Fu RSC Adv Chemistry Eleven novel uncommon single ether linkage dimeric 2-(2-phenylethyl)chromones (aquilasinenones A–K) were isolated by a UPLC-MS guided method from artificial hole-induced agarwood originating from Aquilaria sinensis. Their structures were unambiguously deduced using HRESIMS data, detailed 1D and 2D NMR spectroscopic analysis, and experimental ECD spectra. All the compounds were tested for acetylcholinesterase (AChE) inhibitory activity by Ellman's colorimetric method, and compounds 9–11 displayed weak AChE inhibitory activity with the inhibition ranging from 15.6% to 16.8% at a concentration of 50 μg mL(−1). The Royal Society of Chemistry 2019-05-31 /pmc/articles/PMC9064565/ /pubmed/35519867 http://dx.doi.org/10.1039/c9ra02597a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Kuang, Tongdong
Chen, Hui-Qin
Wang, Hao
Kong, Fan-Dong
Cai, Cai-Hong
Dong, Wen-Hua
Yuan, Jing-Zhe
Mei, Wen-Li
Dai, Hao-Fu
UPLC-MS-guided isolation of single ether linkage dimeric 2-(2-phenylethyl)chromones from Aquilaria sinensis
title UPLC-MS-guided isolation of single ether linkage dimeric 2-(2-phenylethyl)chromones from Aquilaria sinensis
title_full UPLC-MS-guided isolation of single ether linkage dimeric 2-(2-phenylethyl)chromones from Aquilaria sinensis
title_fullStr UPLC-MS-guided isolation of single ether linkage dimeric 2-(2-phenylethyl)chromones from Aquilaria sinensis
title_full_unstemmed UPLC-MS-guided isolation of single ether linkage dimeric 2-(2-phenylethyl)chromones from Aquilaria sinensis
title_short UPLC-MS-guided isolation of single ether linkage dimeric 2-(2-phenylethyl)chromones from Aquilaria sinensis
title_sort uplc-ms-guided isolation of single ether linkage dimeric 2-(2-phenylethyl)chromones from aquilaria sinensis
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9064565/
https://www.ncbi.nlm.nih.gov/pubmed/35519867
http://dx.doi.org/10.1039/c9ra02597a
work_keys_str_mv AT kuangtongdong uplcmsguidedisolationofsingleetherlinkagedimeric22phenylethylchromonesfromaquilariasinensis
AT chenhuiqin uplcmsguidedisolationofsingleetherlinkagedimeric22phenylethylchromonesfromaquilariasinensis
AT wanghao uplcmsguidedisolationofsingleetherlinkagedimeric22phenylethylchromonesfromaquilariasinensis
AT kongfandong uplcmsguidedisolationofsingleetherlinkagedimeric22phenylethylchromonesfromaquilariasinensis
AT caicaihong uplcmsguidedisolationofsingleetherlinkagedimeric22phenylethylchromonesfromaquilariasinensis
AT dongwenhua uplcmsguidedisolationofsingleetherlinkagedimeric22phenylethylchromonesfromaquilariasinensis
AT yuanjingzhe uplcmsguidedisolationofsingleetherlinkagedimeric22phenylethylchromonesfromaquilariasinensis
AT meiwenli uplcmsguidedisolationofsingleetherlinkagedimeric22phenylethylchromonesfromaquilariasinensis
AT daihaofu uplcmsguidedisolationofsingleetherlinkagedimeric22phenylethylchromonesfromaquilariasinensis