Eutypenoids A–C: Novel Pimarane Diterpenoids from the Arctic Fungus Eutypella sp. D-1
Eutypenoids A–C (1–3), pimarane diterpenoid alkaloid and two ring A rearranged pimarane diterpenoids, were isolated from the culture of Eutypella sp. D-1 obtained from high-latitude soil of the Arctic. Their structures, including absolute configurations, were authenticated on the basis of the mass s...
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ftpubmed:oai:pubmedcentral.nih.gov:4820298 2023-05-15T14:48:58+02:00 Eutypenoids A–C: Novel Pimarane Diterpenoids from the Arctic Fungus Eutypella sp. D-1 Zhang, Liu-Qiang Chen, Xiao-Chong Chen, Zhao-Qiang Wang, Gui-Min Zhu, Shi-Guo Yang, Yi-Fu Chen, Kai-Xian Liu, Xiao-Yu Li, Yi-Ming 2016-03-07 http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4820298/ http://www.ncbi.nlm.nih.gov/pubmed/26959036 https://doi.org/10.3390/md14030044 en eng MDPI http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4820298/ http://www.ncbi.nlm.nih.gov/pubmed/26959036 http://dx.doi.org/10.3390/md14030044 © 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 by Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/). CC-BY Article Text 2016 ftpubmed https://doi.org/10.3390/md14030044 2016-04-10T00:21:20Z Eutypenoids A–C (1–3), pimarane diterpenoid alkaloid and two ring A rearranged pimarane diterpenoids, were isolated from the culture of Eutypella sp. D-1 obtained from high-latitude soil of the Arctic. Their structures, including absolute configurations, were authenticated on the basis of the mass spectroscopy (MS), nuclear magnetic resonance (NMR), X-ray crystallography, and electronic circular dichroism (ECD) analysis. The immunosuppressive effects of eutypenoids A–C (1–3) were studied using a ConA-induced splenocyte proliferation model, which suggested that 2 exhibited potent immunosuppressive activities. Text Arctic PubMed Central (PMC) Arctic Marine Drugs 14 3 44 |
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Article Zhang, Liu-Qiang Chen, Xiao-Chong Chen, Zhao-Qiang Wang, Gui-Min Zhu, Shi-Guo Yang, Yi-Fu Chen, Kai-Xian Liu, Xiao-Yu Li, Yi-Ming Eutypenoids A–C: Novel Pimarane Diterpenoids from the Arctic Fungus Eutypella sp. D-1 |
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Article |
description |
Eutypenoids A–C (1–3), pimarane diterpenoid alkaloid and two ring A rearranged pimarane diterpenoids, were isolated from the culture of Eutypella sp. D-1 obtained from high-latitude soil of the Arctic. Their structures, including absolute configurations, were authenticated on the basis of the mass spectroscopy (MS), nuclear magnetic resonance (NMR), X-ray crystallography, and electronic circular dichroism (ECD) analysis. The immunosuppressive effects of eutypenoids A–C (1–3) were studied using a ConA-induced splenocyte proliferation model, which suggested that 2 exhibited potent immunosuppressive activities. |
format |
Text |
author |
Zhang, Liu-Qiang Chen, Xiao-Chong Chen, Zhao-Qiang Wang, Gui-Min Zhu, Shi-Guo Yang, Yi-Fu Chen, Kai-Xian Liu, Xiao-Yu Li, Yi-Ming |
author_facet |
Zhang, Liu-Qiang Chen, Xiao-Chong Chen, Zhao-Qiang Wang, Gui-Min Zhu, Shi-Guo Yang, Yi-Fu Chen, Kai-Xian Liu, Xiao-Yu Li, Yi-Ming |
author_sort |
Zhang, Liu-Qiang |
title |
Eutypenoids A–C: Novel Pimarane Diterpenoids from the Arctic Fungus Eutypella sp. D-1 |
title_short |
Eutypenoids A–C: Novel Pimarane Diterpenoids from the Arctic Fungus Eutypella sp. D-1 |
title_full |
Eutypenoids A–C: Novel Pimarane Diterpenoids from the Arctic Fungus Eutypella sp. D-1 |
title_fullStr |
Eutypenoids A–C: Novel Pimarane Diterpenoids from the Arctic Fungus Eutypella sp. D-1 |
title_full_unstemmed |
Eutypenoids A–C: Novel Pimarane Diterpenoids from the Arctic Fungus Eutypella sp. D-1 |
title_sort |
eutypenoids a–c: novel pimarane diterpenoids from the arctic fungus eutypella sp. d-1 |
publisher |
MDPI |
publishDate |
2016 |
url |
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4820298/ http://www.ncbi.nlm.nih.gov/pubmed/26959036 https://doi.org/10.3390/md14030044 |
geographic |
Arctic |
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Arctic |
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Arctic |
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Arctic |
op_relation |
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4820298/ http://www.ncbi.nlm.nih.gov/pubmed/26959036 http://dx.doi.org/10.3390/md14030044 |
op_rights |
© 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 by Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/). |
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https://doi.org/10.3390/md14030044 |
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Marine Drugs |
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14 |
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44 |
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