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Isolation and Synthesis of a Bioactive Benzenoid Derivative from the Fruiting Bodies of Antrodia camphorata

A new enynyl-benzenoid, antrocamphin O (1,4,7-dimethoxy-5-methyl-6-(3′-methylbut-3-en-1-ynyl)benzo[d][1,3]dioxide), and the known benzenoids antrocamphin A and 7-dimethoxy-5-methyl-1,3-benzodioxole, were isolated from the fruiting bodies of Antrodia camphorata (Taiwanofungus camphoratus). The struct...

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Autores principales: Chen, Pi-Yu, Wu, Jen-Der, Tang, Kai-Yih, Yu, Chieh-Chou, Kuo, Yueh-Hsiung, Zhong, Wen-Bin, Lee, Ching-Kuo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270037/
https://www.ncbi.nlm.nih.gov/pubmed/23812251
http://dx.doi.org/10.3390/molecules18077600
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author Chen, Pi-Yu
Wu, Jen-Der
Tang, Kai-Yih
Yu, Chieh-Chou
Kuo, Yueh-Hsiung
Zhong, Wen-Bin
Lee, Ching-Kuo
author_facet Chen, Pi-Yu
Wu, Jen-Der
Tang, Kai-Yih
Yu, Chieh-Chou
Kuo, Yueh-Hsiung
Zhong, Wen-Bin
Lee, Ching-Kuo
author_sort Chen, Pi-Yu
collection PubMed
description A new enynyl-benzenoid, antrocamphin O (1,4,7-dimethoxy-5-methyl-6-(3′-methylbut-3-en-1-ynyl)benzo[d][1,3]dioxide), and the known benzenoids antrocamphin A and 7-dimethoxy-5-methyl-1,3-benzodioxole, were isolated from the fruiting bodies of Antrodia camphorata (Taiwanofungus camphoratus). The structure of antrocamphin O was unambiguously assigned by the analysis of spectral data (including 1D and 2D NMR, high-resolution MS, IR, and UV) and total synthesis. Compound 1 was prepared through the Sonogashira reaction of 5-iodo-4,7-dimethoxy-6-methylbenzene and 2-methylbut-1-en-3-yne as the key step. The benzenoids were tested for cytotoxicity against the HT29, HTC15, DLD-1, and COLO 205 colon cancer cell lines, andactivities are reported herein.
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spelling pubmed-62700372018-12-17 Isolation and Synthesis of a Bioactive Benzenoid Derivative from the Fruiting Bodies of Antrodia camphorata Chen, Pi-Yu Wu, Jen-Der Tang, Kai-Yih Yu, Chieh-Chou Kuo, Yueh-Hsiung Zhong, Wen-Bin Lee, Ching-Kuo Molecules Article A new enynyl-benzenoid, antrocamphin O (1,4,7-dimethoxy-5-methyl-6-(3′-methylbut-3-en-1-ynyl)benzo[d][1,3]dioxide), and the known benzenoids antrocamphin A and 7-dimethoxy-5-methyl-1,3-benzodioxole, were isolated from the fruiting bodies of Antrodia camphorata (Taiwanofungus camphoratus). The structure of antrocamphin O was unambiguously assigned by the analysis of spectral data (including 1D and 2D NMR, high-resolution MS, IR, and UV) and total synthesis. Compound 1 was prepared through the Sonogashira reaction of 5-iodo-4,7-dimethoxy-6-methylbenzene and 2-methylbut-1-en-3-yne as the key step. The benzenoids were tested for cytotoxicity against the HT29, HTC15, DLD-1, and COLO 205 colon cancer cell lines, andactivities are reported herein. MDPI 2013-06-28 /pmc/articles/PMC6270037/ /pubmed/23812251 http://dx.doi.org/10.3390/molecules18077600 Text en © 2013 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
Chen, Pi-Yu
Wu, Jen-Der
Tang, Kai-Yih
Yu, Chieh-Chou
Kuo, Yueh-Hsiung
Zhong, Wen-Bin
Lee, Ching-Kuo
Isolation and Synthesis of a Bioactive Benzenoid Derivative from the Fruiting Bodies of Antrodia camphorata
title Isolation and Synthesis of a Bioactive Benzenoid Derivative from the Fruiting Bodies of Antrodia camphorata
title_full Isolation and Synthesis of a Bioactive Benzenoid Derivative from the Fruiting Bodies of Antrodia camphorata
title_fullStr Isolation and Synthesis of a Bioactive Benzenoid Derivative from the Fruiting Bodies of Antrodia camphorata
title_full_unstemmed Isolation and Synthesis of a Bioactive Benzenoid Derivative from the Fruiting Bodies of Antrodia camphorata
title_short Isolation and Synthesis of a Bioactive Benzenoid Derivative from the Fruiting Bodies of Antrodia camphorata
title_sort isolation and synthesis of a bioactive benzenoid derivative from the fruiting bodies of antrodia camphorata
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270037/
https://www.ncbi.nlm.nih.gov/pubmed/23812251
http://dx.doi.org/10.3390/molecules18077600
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