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Spiculisporic Acids B–D, Three New γ-Butenolide Derivatives from a Sea Urchin-Derived Fungus Aspergillus sp. HDf2
Three new γ-butenolide derivatives 1–3, named spiculisporic acids B–D, were isolated from the culture of Aspergillus sp. HDf2, a marine-derived fungus that resides in the sea urchin, Anthocidaris crassispina. The structures of 1–3 were elucidated on the basis of spectroscopic methods, including MS a...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268229/ https://www.ncbi.nlm.nih.gov/pubmed/23128094 http://dx.doi.org/10.3390/molecules171113175 |
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author | Wang, Rong Liu, Tian-Mi Shen, Ming-Hui Yang, Ming-Qiu Feng, Quan-Ying Tang, Xian-Ming Li, Xiang-Min |
author_facet | Wang, Rong Liu, Tian-Mi Shen, Ming-Hui Yang, Ming-Qiu Feng, Quan-Ying Tang, Xian-Ming Li, Xiang-Min |
author_sort | Wang, Rong |
collection | PubMed |
description | Three new γ-butenolide derivatives 1–3, named spiculisporic acids B–D, were isolated from the culture of Aspergillus sp. HDf2, a marine-derived fungus that resides in the sea urchin, Anthocidaris crassispina. The structures of 1–3 were elucidated on the basis of spectroscopic methods, including MS and 2D NMR techniques. Their in vitro cytotoxic activities against two cell lines (SGC-7901, human gastric adenocarcinoma and SPC-A-1, human lung adenocarcinoma) and inhibitory activities against Staphylococcus aureus ATCC 51650 were investigated. |
format | Online Article Text |
id | pubmed-6268229 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62682292018-12-13 Spiculisporic Acids B–D, Three New γ-Butenolide Derivatives from a Sea Urchin-Derived Fungus Aspergillus sp. HDf2 Wang, Rong Liu, Tian-Mi Shen, Ming-Hui Yang, Ming-Qiu Feng, Quan-Ying Tang, Xian-Ming Li, Xiang-Min Molecules Addendum Three new γ-butenolide derivatives 1–3, named spiculisporic acids B–D, were isolated from the culture of Aspergillus sp. HDf2, a marine-derived fungus that resides in the sea urchin, Anthocidaris crassispina. The structures of 1–3 were elucidated on the basis of spectroscopic methods, including MS and 2D NMR techniques. Their in vitro cytotoxic activities against two cell lines (SGC-7901, human gastric adenocarcinoma and SPC-A-1, human lung adenocarcinoma) and inhibitory activities against Staphylococcus aureus ATCC 51650 were investigated. MDPI 2012-11-05 /pmc/articles/PMC6268229/ /pubmed/23128094 http://dx.doi.org/10.3390/molecules171113175 Text en © 2012 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ 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 | Addendum Wang, Rong Liu, Tian-Mi Shen, Ming-Hui Yang, Ming-Qiu Feng, Quan-Ying Tang, Xian-Ming Li, Xiang-Min Spiculisporic Acids B–D, Three New γ-Butenolide Derivatives from a Sea Urchin-Derived Fungus Aspergillus sp. HDf2 |
title | Spiculisporic Acids B–D, Three New γ-Butenolide Derivatives from a Sea Urchin-Derived Fungus Aspergillus sp. HDf2 |
title_full | Spiculisporic Acids B–D, Three New γ-Butenolide Derivatives from a Sea Urchin-Derived Fungus Aspergillus sp. HDf2 |
title_fullStr | Spiculisporic Acids B–D, Three New γ-Butenolide Derivatives from a Sea Urchin-Derived Fungus Aspergillus sp. HDf2 |
title_full_unstemmed | Spiculisporic Acids B–D, Three New γ-Butenolide Derivatives from a Sea Urchin-Derived Fungus Aspergillus sp. HDf2 |
title_short | Spiculisporic Acids B–D, Three New γ-Butenolide Derivatives from a Sea Urchin-Derived Fungus Aspergillus sp. HDf2 |
title_sort | spiculisporic acids b–d, three new γ-butenolide derivatives from a sea urchin-derived fungus aspergillus sp. hdf2 |
topic | Addendum |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268229/ https://www.ncbi.nlm.nih.gov/pubmed/23128094 http://dx.doi.org/10.3390/molecules171113175 |
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