Cargando…

Three New Butenolides from the Fungus Aspergillus sp. CBS-P-2

Three new butenolides aspernolides H–J (1–3) together with seven known ones (4–10) were isolated from the fungus Aspergillus sp. CBS-P-2. Their chemical structures were established on the basis of 1D- and 2D-NMR spectroscopic data, HR-ESI-MS analysis, and their absolute configuration were determined...

Descripción completa

Detalles Bibliográficos
Autores principales: An, Xiao, Pei, Yuehu, Chen, Shaofei, Li, Shengge, Hu, Xiaolong, Chen, Gang, Lin, Bin, Wang, Haifeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273075/
https://www.ncbi.nlm.nih.gov/pubmed/27754391
http://dx.doi.org/10.3390/molecules21101361
_version_ 1783377301075918848
author An, Xiao
Pei, Yuehu
Chen, Shaofei
Li, Shengge
Hu, Xiaolong
Chen, Gang
Lin, Bin
Wang, Haifeng
author_facet An, Xiao
Pei, Yuehu
Chen, Shaofei
Li, Shengge
Hu, Xiaolong
Chen, Gang
Lin, Bin
Wang, Haifeng
author_sort An, Xiao
collection PubMed
description Three new butenolides aspernolides H–J (1–3) together with seven known ones (4–10) were isolated from the fungus Aspergillus sp. CBS-P-2. Their chemical structures were established on the basis of 1D- and 2D-NMR spectroscopic data, HR-ESI-MS analysis, and their absolute configuration were determined by circular dichroism (CD) analysis. All the compounds were evaluated for the antioxidant effects by DPPH and ABTS methods, the antitumor activities against four human tumor cell lines (HL-60, ASPC1, HCT-116 and PC-3) and antimicrobial activities. Compounds 4–10 showed significant activity against DPPH (IC(50) = 15.9–34.3 μM) and compounds 1–10 exhibited significant ABTS free radical scavenging activity (IC(50) = 2.8–33.1 μM). Compounds 2, 5 and 11 showed potent cytotoxic activities against HL-60 cell lines with IC(50) values of 39.4, 13.2 and 16.3 μM, respectively. Compound 10 showed good antimicrobial activity against Staphylococcus aureus with minimum inhibitory concentration (MIC) of 21.3 μM.
format Online
Article
Text
id pubmed-6273075
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-62730752018-12-28 Three New Butenolides from the Fungus Aspergillus sp. CBS-P-2 An, Xiao Pei, Yuehu Chen, Shaofei Li, Shengge Hu, Xiaolong Chen, Gang Lin, Bin Wang, Haifeng Molecules Article Three new butenolides aspernolides H–J (1–3) together with seven known ones (4–10) were isolated from the fungus Aspergillus sp. CBS-P-2. Their chemical structures were established on the basis of 1D- and 2D-NMR spectroscopic data, HR-ESI-MS analysis, and their absolute configuration were determined by circular dichroism (CD) analysis. All the compounds were evaluated for the antioxidant effects by DPPH and ABTS methods, the antitumor activities against four human tumor cell lines (HL-60, ASPC1, HCT-116 and PC-3) and antimicrobial activities. Compounds 4–10 showed significant activity against DPPH (IC(50) = 15.9–34.3 μM) and compounds 1–10 exhibited significant ABTS free radical scavenging activity (IC(50) = 2.8–33.1 μM). Compounds 2, 5 and 11 showed potent cytotoxic activities against HL-60 cell lines with IC(50) values of 39.4, 13.2 and 16.3 μM, respectively. Compound 10 showed good antimicrobial activity against Staphylococcus aureus with minimum inhibitory concentration (MIC) of 21.3 μM. MDPI 2016-10-13 /pmc/articles/PMC6273075/ /pubmed/27754391 http://dx.doi.org/10.3390/molecules21101361 Text en © 2016 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
An, Xiao
Pei, Yuehu
Chen, Shaofei
Li, Shengge
Hu, Xiaolong
Chen, Gang
Lin, Bin
Wang, Haifeng
Three New Butenolides from the Fungus Aspergillus sp. CBS-P-2
title Three New Butenolides from the Fungus Aspergillus sp. CBS-P-2
title_full Three New Butenolides from the Fungus Aspergillus sp. CBS-P-2
title_fullStr Three New Butenolides from the Fungus Aspergillus sp. CBS-P-2
title_full_unstemmed Three New Butenolides from the Fungus Aspergillus sp. CBS-P-2
title_short Three New Butenolides from the Fungus Aspergillus sp. CBS-P-2
title_sort three new butenolides from the fungus aspergillus sp. cbs-p-2
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273075/
https://www.ncbi.nlm.nih.gov/pubmed/27754391
http://dx.doi.org/10.3390/molecules21101361
work_keys_str_mv AT anxiao threenewbutenolidesfromthefungusaspergillusspcbsp2
AT peiyuehu threenewbutenolidesfromthefungusaspergillusspcbsp2
AT chenshaofei threenewbutenolidesfromthefungusaspergillusspcbsp2
AT lishengge threenewbutenolidesfromthefungusaspergillusspcbsp2
AT huxiaolong threenewbutenolidesfromthefungusaspergillusspcbsp2
AT chengang threenewbutenolidesfromthefungusaspergillusspcbsp2
AT linbin threenewbutenolidesfromthefungusaspergillusspcbsp2
AT wanghaifeng threenewbutenolidesfromthefungusaspergillusspcbsp2