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Cytotoxic Polyketides from a Deep-Sea Sediment Derived Fungus Diaporthe phaseolorum FS431

Two new chromone-derived polyketides phaseolorins, G and H (1 and 2), and one new anthraquinone derivative, phaseolorin I (3), together with three known compounds (4–6), were isolated from the deep-sea sediment-derived fungus Diaporthe phaseolorum FS431. The structures of the new compounds were dete...

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Autores principales: Niu, Zheng, Chen, Yuchan, Guo, Heng, Li, Sai-Ni, Li, Hao-Hua, Liu, Hong-Xin, Liu, Zhaoming, Zhang, Weimin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6749523/
https://www.ncbi.nlm.nih.gov/pubmed/31443573
http://dx.doi.org/10.3390/molecules24173062
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author Niu, Zheng
Chen, Yuchan
Guo, Heng
Li, Sai-Ni
Li, Hao-Hua
Liu, Hong-Xin
Liu, Zhaoming
Zhang, Weimin
author_facet Niu, Zheng
Chen, Yuchan
Guo, Heng
Li, Sai-Ni
Li, Hao-Hua
Liu, Hong-Xin
Liu, Zhaoming
Zhang, Weimin
author_sort Niu, Zheng
collection PubMed
description Two new chromone-derived polyketides phaseolorins, G and H (1 and 2), and one new anthraquinone derivative, phaseolorin I (3), together with three known compounds (4–6), were isolated from the deep-sea sediment-derived fungus Diaporthe phaseolorum FS431. The structures of the new compounds were determined by comprehensive analysis of their spectroscopic data, and the absolute configuration of 1 was established by quantum chemical calculations of electron capture detection (ECD). All the isolated compounds (1–6) were tested for their in vitro cytotoxic activities against four human tumor cell lines, of which compound 4 exhibited significant effect against MCF-7, HepG-2, and A549 tumor cell lines with IC(50) values of 2.60, 2.55, and 4.64 µM, respectively.
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spelling pubmed-67495232019-09-27 Cytotoxic Polyketides from a Deep-Sea Sediment Derived Fungus Diaporthe phaseolorum FS431 Niu, Zheng Chen, Yuchan Guo, Heng Li, Sai-Ni Li, Hao-Hua Liu, Hong-Xin Liu, Zhaoming Zhang, Weimin Molecules Article Two new chromone-derived polyketides phaseolorins, G and H (1 and 2), and one new anthraquinone derivative, phaseolorin I (3), together with three known compounds (4–6), were isolated from the deep-sea sediment-derived fungus Diaporthe phaseolorum FS431. The structures of the new compounds were determined by comprehensive analysis of their spectroscopic data, and the absolute configuration of 1 was established by quantum chemical calculations of electron capture detection (ECD). All the isolated compounds (1–6) were tested for their in vitro cytotoxic activities against four human tumor cell lines, of which compound 4 exhibited significant effect against MCF-7, HepG-2, and A549 tumor cell lines with IC(50) values of 2.60, 2.55, and 4.64 µM, respectively. MDPI 2019-08-22 /pmc/articles/PMC6749523/ /pubmed/31443573 http://dx.doi.org/10.3390/molecules24173062 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
Niu, Zheng
Chen, Yuchan
Guo, Heng
Li, Sai-Ni
Li, Hao-Hua
Liu, Hong-Xin
Liu, Zhaoming
Zhang, Weimin
Cytotoxic Polyketides from a Deep-Sea Sediment Derived Fungus Diaporthe phaseolorum FS431
title Cytotoxic Polyketides from a Deep-Sea Sediment Derived Fungus Diaporthe phaseolorum FS431
title_full Cytotoxic Polyketides from a Deep-Sea Sediment Derived Fungus Diaporthe phaseolorum FS431
title_fullStr Cytotoxic Polyketides from a Deep-Sea Sediment Derived Fungus Diaporthe phaseolorum FS431
title_full_unstemmed Cytotoxic Polyketides from a Deep-Sea Sediment Derived Fungus Diaporthe phaseolorum FS431
title_short Cytotoxic Polyketides from a Deep-Sea Sediment Derived Fungus Diaporthe phaseolorum FS431
title_sort cytotoxic polyketides from a deep-sea sediment derived fungus diaporthe phaseolorum fs431
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6749523/
https://www.ncbi.nlm.nih.gov/pubmed/31443573
http://dx.doi.org/10.3390/molecules24173062
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