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Three New 2-(2-Phenylethyl)chromone Derivatives of Agarwood Originated from Gyrinops salicifolia

Two new 2-(2-phenylethyl)chromone derivatives (1–2), comprising 5,6,7,8-tetrahydro-2-(2-phenylethyl)chromone and benzylacetone moieties, together with one new 2-(2-phenylethenyl)chromone (3) were isolated from the ethyl acetate extraction of agarwood originated from Gyrinops salicifolia Ridl. All st...

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Autores principales: Dong, Wen-Hua, Wang, Hao, Guo, Feng-Juan, Mei, Wen-Li, Chen, Hui-Qin, Kong, Fan-Dong, Li, Wei, Zhou, Kai-Bing, Dai, Hao-Fu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6384947/
https://www.ncbi.nlm.nih.gov/pubmed/30736275
http://dx.doi.org/10.3390/molecules24030576
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author Dong, Wen-Hua
Wang, Hao
Guo, Feng-Juan
Mei, Wen-Li
Chen, Hui-Qin
Kong, Fan-Dong
Li, Wei
Zhou, Kai-Bing
Dai, Hao-Fu
author_facet Dong, Wen-Hua
Wang, Hao
Guo, Feng-Juan
Mei, Wen-Li
Chen, Hui-Qin
Kong, Fan-Dong
Li, Wei
Zhou, Kai-Bing
Dai, Hao-Fu
author_sort Dong, Wen-Hua
collection PubMed
description Two new 2-(2-phenylethyl)chromone derivatives (1–2), comprising 5,6,7,8-tetrahydro-2-(2-phenylethyl)chromone and benzylacetone moieties, together with one new 2-(2-phenylethenyl)chromone (3) were isolated from the ethyl acetate extraction of agarwood originated from Gyrinops salicifolia Ridl. All structures were unambiguously elucidated on the basis of 1D and 2D NMR spectra as well as by HRESIMS data. All isolated compounds were tested for acetylcholinesterase (AChE) inhibitory activity and cytotoxic activity against human myeloid leukemia cell line (K562). However, none of the compounds displayed AChE inhibitory activity at a concentration of 50 µg mL(−1) or cytotoxic activity against K562 cell line.
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spelling pubmed-63849472019-02-23 Three New 2-(2-Phenylethyl)chromone Derivatives of Agarwood Originated from Gyrinops salicifolia Dong, Wen-Hua Wang, Hao Guo, Feng-Juan Mei, Wen-Li Chen, Hui-Qin Kong, Fan-Dong Li, Wei Zhou, Kai-Bing Dai, Hao-Fu Molecules Article Two new 2-(2-phenylethyl)chromone derivatives (1–2), comprising 5,6,7,8-tetrahydro-2-(2-phenylethyl)chromone and benzylacetone moieties, together with one new 2-(2-phenylethenyl)chromone (3) were isolated from the ethyl acetate extraction of agarwood originated from Gyrinops salicifolia Ridl. All structures were unambiguously elucidated on the basis of 1D and 2D NMR spectra as well as by HRESIMS data. All isolated compounds were tested for acetylcholinesterase (AChE) inhibitory activity and cytotoxic activity against human myeloid leukemia cell line (K562). However, none of the compounds displayed AChE inhibitory activity at a concentration of 50 µg mL(−1) or cytotoxic activity against K562 cell line. MDPI 2019-02-06 /pmc/articles/PMC6384947/ /pubmed/30736275 http://dx.doi.org/10.3390/molecules24030576 Text en © 2019 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
Dong, Wen-Hua
Wang, Hao
Guo, Feng-Juan
Mei, Wen-Li
Chen, Hui-Qin
Kong, Fan-Dong
Li, Wei
Zhou, Kai-Bing
Dai, Hao-Fu
Three New 2-(2-Phenylethyl)chromone Derivatives of Agarwood Originated from Gyrinops salicifolia
title Three New 2-(2-Phenylethyl)chromone Derivatives of Agarwood Originated from Gyrinops salicifolia
title_full Three New 2-(2-Phenylethyl)chromone Derivatives of Agarwood Originated from Gyrinops salicifolia
title_fullStr Three New 2-(2-Phenylethyl)chromone Derivatives of Agarwood Originated from Gyrinops salicifolia
title_full_unstemmed Three New 2-(2-Phenylethyl)chromone Derivatives of Agarwood Originated from Gyrinops salicifolia
title_short Three New 2-(2-Phenylethyl)chromone Derivatives of Agarwood Originated from Gyrinops salicifolia
title_sort three new 2-(2-phenylethyl)chromone derivatives of agarwood originated from gyrinops salicifolia
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6384947/
https://www.ncbi.nlm.nih.gov/pubmed/30736275
http://dx.doi.org/10.3390/molecules24030576
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