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Nine New and Five Known Polyketides Derived from a Deep Sea-Sourced Aspergillus sp. 16-02-1

Nine new C(9) polyketides, named aspiketolactonol (1), aspilactonols A–F (2–7), aspyronol (9) and epiaspinonediol (11), were isolated together with five known polyketides, (S)-2-(2′-hydroxyethyl)-4-methyl-γ-butyrolactone (8), dihydroaspyrone (10), aspinotriol A (12), aspinotriol B (13) and chaetoqua...

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Autores principales: Chen, Xiu-Wen, Li, Chang-Wei, Cui, Cheng-Bin, Hua, Wei, Zhu, Tian-Jiao, Gu, Qian-Qun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4071568/
https://www.ncbi.nlm.nih.gov/pubmed/24871461
http://dx.doi.org/10.3390/md12063116
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author Chen, Xiu-Wen
Li, Chang-Wei
Cui, Cheng-Bin
Hua, Wei
Zhu, Tian-Jiao
Gu, Qian-Qun
author_facet Chen, Xiu-Wen
Li, Chang-Wei
Cui, Cheng-Bin
Hua, Wei
Zhu, Tian-Jiao
Gu, Qian-Qun
author_sort Chen, Xiu-Wen
collection PubMed
description Nine new C(9) polyketides, named aspiketolactonol (1), aspilactonols A–F (2–7), aspyronol (9) and epiaspinonediol (11), were isolated together with five known polyketides, (S)-2-(2′-hydroxyethyl)-4-methyl-γ-butyrolactone (8), dihydroaspyrone (10), aspinotriol A (12), aspinotriol B (13) and chaetoquadrin F (14), from the secondary metabolites of an Aspergillus sp. 16-02-1 that was isolated from a deep-sea sediment sample. Structures of the new compounds, including their absolute configurations, were determined by spectroscopic methods, especially the 2D NMR, circular dichroism (CD), Mo(2)-induced CD and Mosher’s (1)H NMR analyses. Compound 8 was isolated from natural sources for the first time, and the possible biosynthetic pathways for 1–14 were also proposed and discussed. Compounds 1–14 inhibited human cancer cell lines, K562, HL-60, HeLa and BGC-823, to varying extents.
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spelling pubmed-40715682014-06-26 Nine New and Five Known Polyketides Derived from a Deep Sea-Sourced Aspergillus sp. 16-02-1 Chen, Xiu-Wen Li, Chang-Wei Cui, Cheng-Bin Hua, Wei Zhu, Tian-Jiao Gu, Qian-Qun Mar Drugs Article Nine new C(9) polyketides, named aspiketolactonol (1), aspilactonols A–F (2–7), aspyronol (9) and epiaspinonediol (11), were isolated together with five known polyketides, (S)-2-(2′-hydroxyethyl)-4-methyl-γ-butyrolactone (8), dihydroaspyrone (10), aspinotriol A (12), aspinotriol B (13) and chaetoquadrin F (14), from the secondary metabolites of an Aspergillus sp. 16-02-1 that was isolated from a deep-sea sediment sample. Structures of the new compounds, including their absolute configurations, were determined by spectroscopic methods, especially the 2D NMR, circular dichroism (CD), Mo(2)-induced CD and Mosher’s (1)H NMR analyses. Compound 8 was isolated from natural sources for the first time, and the possible biosynthetic pathways for 1–14 were also proposed and discussed. Compounds 1–14 inhibited human cancer cell lines, K562, HL-60, HeLa and BGC-823, to varying extents. MDPI 2014-05-27 /pmc/articles/PMC4071568/ /pubmed/24871461 http://dx.doi.org/10.3390/md12063116 Text en © 2014 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, Xiu-Wen
Li, Chang-Wei
Cui, Cheng-Bin
Hua, Wei
Zhu, Tian-Jiao
Gu, Qian-Qun
Nine New and Five Known Polyketides Derived from a Deep Sea-Sourced Aspergillus sp. 16-02-1
title Nine New and Five Known Polyketides Derived from a Deep Sea-Sourced Aspergillus sp. 16-02-1
title_full Nine New and Five Known Polyketides Derived from a Deep Sea-Sourced Aspergillus sp. 16-02-1
title_fullStr Nine New and Five Known Polyketides Derived from a Deep Sea-Sourced Aspergillus sp. 16-02-1
title_full_unstemmed Nine New and Five Known Polyketides Derived from a Deep Sea-Sourced Aspergillus sp. 16-02-1
title_short Nine New and Five Known Polyketides Derived from a Deep Sea-Sourced Aspergillus sp. 16-02-1
title_sort nine new and five known polyketides derived from a deep sea-sourced aspergillus sp. 16-02-1
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4071568/
https://www.ncbi.nlm.nih.gov/pubmed/24871461
http://dx.doi.org/10.3390/md12063116
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