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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...

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Autores principales: Wang, Rong, Liu, Tian-Mi, Shen, Ming-Hui, Yang, Ming-Qiu, Feng, Quan-Ying, Tang, Xian-Ming, Li, Xiang-Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2012
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.
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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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