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: Hao-Bing Yu, Xiao-Li Wang, Wei-Heng Xu, Yi-Xin Zhang, Yi-Sen Qian, Jian-Peng Zhang, Xiao-Ling Lu, Xiao-Yu Liu
Format: Article in Journal/Newspaper
Language:English
Published: MDPI AG 2018
Subjects:
Online Access:https://doi.org/10.3390/md16080284
https://doaj.org/article/a1cf1f561b2f4d389b2337b6f8998f8d
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spelling ftdoajarticles:oai:doaj.org/article:a1cf1f561b2f4d389b2337b6f8998f8d 2023-05-15T14:49:41+02:00 Eutypellenoids A–C, New Pimarane Diterpenes from the Arctic Fungus Eutypella sp. D-1 Hao-Bing Yu Xiao-Li Wang Wei-Heng Xu Yi-Xin Zhang Yi-Sen Qian Jian-Peng Zhang Xiao-Ling Lu Xiao-Yu Liu 2018-08-01T00:00:00Z https://doi.org/10.3390/md16080284 https://doaj.org/article/a1cf1f561b2f4d389b2337b6f8998f8d EN eng MDPI AG http://www.mdpi.com/1660-3397/16/8/284 https://doaj.org/toc/1660-3397 1660-3397 doi:10.3390/md16080284 https://doaj.org/article/a1cf1f561b2f4d389b2337b6f8998f8d Marine Drugs, Vol 16, Iss 8, p 284 (2018) Arctic fungus Eutypella sp pimarane diterpene bioactivity Biology (General) QH301-705.5 article 2018 ftdoajarticles https://doi.org/10.3390/md16080284 2022-12-30T19:56:57Z 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. Article in Journal/Newspaper Arctic Directory of Open Access Journals: DOAJ Articles Arctic Marine Drugs 16 8 284
institution Open Polar
collection Directory of Open Access Journals: DOAJ Articles
op_collection_id ftdoajarticles
language English
topic Arctic fungus
Eutypella sp
pimarane diterpene
bioactivity
Biology (General)
QH301-705.5
spellingShingle Arctic fungus
Eutypella sp
pimarane diterpene
bioactivity
Biology (General)
QH301-705.5
Hao-Bing Yu
Xiao-Li Wang
Wei-Heng Xu
Yi-Xin Zhang
Yi-Sen Qian
Jian-Peng Zhang
Xiao-Ling Lu
Xiao-Yu Liu
Eutypellenoids A–C, New Pimarane Diterpenes from the Arctic Fungus Eutypella sp. D-1
topic_facet Arctic fungus
Eutypella sp
pimarane diterpene
bioactivity
Biology (General)
QH301-705.5
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 Article in Journal/Newspaper
author Hao-Bing Yu
Xiao-Li Wang
Wei-Heng Xu
Yi-Xin Zhang
Yi-Sen Qian
Jian-Peng Zhang
Xiao-Ling Lu
Xiao-Yu Liu
author_facet Hao-Bing Yu
Xiao-Li Wang
Wei-Heng Xu
Yi-Xin Zhang
Yi-Sen Qian
Jian-Peng Zhang
Xiao-Ling Lu
Xiao-Yu Liu
author_sort Hao-Bing Yu
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 AG
publishDate 2018
url https://doi.org/10.3390/md16080284
https://doaj.org/article/a1cf1f561b2f4d389b2337b6f8998f8d
geographic Arctic
geographic_facet Arctic
genre Arctic
genre_facet Arctic
op_source Marine Drugs, Vol 16, Iss 8, p 284 (2018)
op_relation http://www.mdpi.com/1660-3397/16/8/284
https://doaj.org/toc/1660-3397
1660-3397
doi:10.3390/md16080284
https://doaj.org/article/a1cf1f561b2f4d389b2337b6f8998f8d
op_doi https://doi.org/10.3390/md16080284
container_title Marine Drugs
container_volume 16
container_issue 8
container_start_page 284
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