Eutypellenoids A–C, New Pimarane Diterpenes from the Arctic Fungus Eutypella sp. D-1

Three new pimarane diterpenes, eutypellenoids A–C (1–3), together with a known compound, eutypenoid C (4), were isolated from the culture extract of Eutypella sp. D-1 derived from the Arctic region. Compounds 1–3 possessed an uncommon tetrahydrofuran-fused pimarane diterpene skeleton. The structures...

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Published in:Marine Drugs
Main Authors: Yu, Hao-Bing, Wang, Xiao-Li, Xu, Wei-Heng, Zhang, Yi-Xin, Qian, Yi-Sen, Zhang, Jian-Peng, Lu, Xiao-Ling, Liu, Xiao-Yu
Format: Text
Language:English
Published: MDPI 2018
Subjects:
Online Access:http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6117666/
http://www.ncbi.nlm.nih.gov/pubmed/30115869
https://doi.org/10.3390/md16080284
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spelling ftpubmed:oai:pubmedcentral.nih.gov:6117666 2023-05-15T14:54:02+02:00 Eutypellenoids A–C, New Pimarane Diterpenes from the Arctic Fungus Eutypella sp. D-1 Yu, Hao-Bing Wang, Xiao-Li Xu, Wei-Heng Zhang, Yi-Xin Qian, Yi-Sen Zhang, Jian-Peng Lu, Xiao-Ling Liu, Xiao-Yu 2018-08-16 http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6117666/ http://www.ncbi.nlm.nih.gov/pubmed/30115869 https://doi.org/10.3390/md16080284 en eng MDPI http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6117666/ http://www.ncbi.nlm.nih.gov/pubmed/30115869 http://dx.doi.org/10.3390/md16080284 © 2018 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/). CC-BY Article Text 2018 ftpubmed https://doi.org/10.3390/md16080284 2018-09-09T00:16:37Z Three new pimarane diterpenes, eutypellenoids A–C (1–3), together with a known compound, eutypenoid C (4), were isolated from the culture extract of Eutypella sp. D-1 derived from the Arctic region. Compounds 1–3 possessed an uncommon tetrahydrofuran-fused pimarane diterpene skeleton. The structures of all compounds were determined by detailed spectroscopic analysis, electronic circular dichroism (ECD) analysis, as well as a comparison with the literature data. Antibacterial, antifungal, and cytotoxic activities of these compounds were evaluated. Compound 2 displayed antibacterial activity against Staphylococcus aureus and Escherichia coli with MIC values of 8 and 8 μg/mL, respectively. Additionally, compound 2 showed antifungal activity against Candida parapsilosis, Candida albicans, Candida glabrata, and Candida tropicalis with MIC values of 8, 8, 16, and 32 μg/mL, respectively. Furthermore, compound 2 exhibited moderate cytotoxic activity against HCT-116 cell line with IC50 value of 3.7 μM. Text Arctic PubMed Central (PMC) Arctic Marine Drugs 16 8 284
institution Open Polar
collection PubMed Central (PMC)
op_collection_id ftpubmed
language English
topic Article
spellingShingle Article
Yu, Hao-Bing
Wang, Xiao-Li
Xu, Wei-Heng
Zhang, Yi-Xin
Qian, Yi-Sen
Zhang, Jian-Peng
Lu, Xiao-Ling
Liu, Xiao-Yu
Eutypellenoids A–C, New Pimarane Diterpenes from the Arctic Fungus Eutypella sp. D-1
topic_facet Article
description Three new pimarane diterpenes, eutypellenoids A–C (1–3), together with a known compound, eutypenoid C (4), were isolated from the culture extract of Eutypella sp. D-1 derived from the Arctic region. Compounds 1–3 possessed an uncommon tetrahydrofuran-fused pimarane diterpene skeleton. The structures of all compounds were determined by detailed spectroscopic analysis, electronic circular dichroism (ECD) analysis, as well as a comparison with the literature data. Antibacterial, antifungal, and cytotoxic activities of these compounds were evaluated. Compound 2 displayed antibacterial activity against Staphylococcus aureus and Escherichia coli with MIC values of 8 and 8 μg/mL, respectively. Additionally, compound 2 showed antifungal activity against Candida parapsilosis, Candida albicans, Candida glabrata, and Candida tropicalis with MIC values of 8, 8, 16, and 32 μg/mL, respectively. Furthermore, compound 2 exhibited moderate cytotoxic activity against HCT-116 cell line with IC50 value of 3.7 μM.
format Text
author Yu, Hao-Bing
Wang, Xiao-Li
Xu, Wei-Heng
Zhang, Yi-Xin
Qian, Yi-Sen
Zhang, Jian-Peng
Lu, Xiao-Ling
Liu, Xiao-Yu
author_facet Yu, Hao-Bing
Wang, Xiao-Li
Xu, Wei-Heng
Zhang, Yi-Xin
Qian, Yi-Sen
Zhang, Jian-Peng
Lu, Xiao-Ling
Liu, Xiao-Yu
author_sort Yu, Hao-Bing
title Eutypellenoids A–C, New Pimarane Diterpenes from the Arctic Fungus Eutypella sp. D-1
title_short Eutypellenoids A–C, New Pimarane Diterpenes from the Arctic Fungus Eutypella sp. D-1
title_full Eutypellenoids A–C, New Pimarane Diterpenes from the Arctic Fungus Eutypella sp. D-1
title_fullStr Eutypellenoids A–C, New Pimarane Diterpenes from the Arctic Fungus Eutypella sp. D-1
title_full_unstemmed Eutypellenoids A–C, New Pimarane Diterpenes from the Arctic Fungus Eutypella sp. D-1
title_sort eutypellenoids a–c, new pimarane diterpenes from the arctic fungus eutypella sp. d-1
publisher MDPI
publishDate 2018
url http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6117666/
http://www.ncbi.nlm.nih.gov/pubmed/30115869
https://doi.org/10.3390/md16080284
geographic Arctic
geographic_facet Arctic
genre Arctic
genre_facet Arctic
op_relation http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6117666/
http://www.ncbi.nlm.nih.gov/pubmed/30115869
http://dx.doi.org/10.3390/md16080284
op_rights © 2018 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/).
op_rightsnorm CC-BY
op_doi https://doi.org/10.3390/md16080284
container_title Marine Drugs
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