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Three New Sesquiterpenoids from the Algal-Derived Fungus Penicillium chermesinum EN-480

Secondary metabolites obtained from marine-derived fungi are rich sources of drug candidates. Three new sesquiterpenoids, chermesiterpenoids A–C (1–3), along with four known alkaloids (4–7), were isolated and identified from the marine red algal-derived fungus Penicillium chermesinum EN-480. The str...

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Autores principales: Hu, Xue-Yi, Li, Xiao-Ming, Yang, Sui-Qun, Liu, Hui, Meng, Ling-Hong, Wang, Bin-Gui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7230704/
https://www.ncbi.nlm.nih.gov/pubmed/32272624
http://dx.doi.org/10.3390/md18040194
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author Hu, Xue-Yi
Li, Xiao-Ming
Yang, Sui-Qun
Liu, Hui
Meng, Ling-Hong
Wang, Bin-Gui
author_facet Hu, Xue-Yi
Li, Xiao-Ming
Yang, Sui-Qun
Liu, Hui
Meng, Ling-Hong
Wang, Bin-Gui
author_sort Hu, Xue-Yi
collection PubMed
description Secondary metabolites obtained from marine-derived fungi are rich sources of drug candidates. Three new sesquiterpenoids, chermesiterpenoids A–C (1–3), along with four known alkaloids (4–7), were isolated and identified from the marine red algal-derived fungus Penicillium chermesinum EN-480. The structures of these new sesquiterpenoids were elucidated using detailed analysis of the NMR data and their relative configurations were elucidated using nuclear overhauser effect spectroscopy (NOESY) spectra as well as gauge-independent atomic orbital (GIAO) NMR shift calculations and DP4+ probability analysis. Their absolute configurations were determined using electronic circular dichroism (ECD) calculations and modified Mosher’s method. Compounds 2 and 3 exhibited potent activities against human and aquatic pathogenic bacteria and plant pathogenic fungi.
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spelling pubmed-72307042020-05-22 Three New Sesquiterpenoids from the Algal-Derived Fungus Penicillium chermesinum EN-480 Hu, Xue-Yi Li, Xiao-Ming Yang, Sui-Qun Liu, Hui Meng, Ling-Hong Wang, Bin-Gui Mar Drugs Article Secondary metabolites obtained from marine-derived fungi are rich sources of drug candidates. Three new sesquiterpenoids, chermesiterpenoids A–C (1–3), along with four known alkaloids (4–7), were isolated and identified from the marine red algal-derived fungus Penicillium chermesinum EN-480. The structures of these new sesquiterpenoids were elucidated using detailed analysis of the NMR data and their relative configurations were elucidated using nuclear overhauser effect spectroscopy (NOESY) spectra as well as gauge-independent atomic orbital (GIAO) NMR shift calculations and DP4+ probability analysis. Their absolute configurations were determined using electronic circular dichroism (ECD) calculations and modified Mosher’s method. Compounds 2 and 3 exhibited potent activities against human and aquatic pathogenic bacteria and plant pathogenic fungi. MDPI 2020-04-07 /pmc/articles/PMC7230704/ /pubmed/32272624 http://dx.doi.org/10.3390/md18040194 Text en © 2020 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
Hu, Xue-Yi
Li, Xiao-Ming
Yang, Sui-Qun
Liu, Hui
Meng, Ling-Hong
Wang, Bin-Gui
Three New Sesquiterpenoids from the Algal-Derived Fungus Penicillium chermesinum EN-480
title Three New Sesquiterpenoids from the Algal-Derived Fungus Penicillium chermesinum EN-480
title_full Three New Sesquiterpenoids from the Algal-Derived Fungus Penicillium chermesinum EN-480
title_fullStr Three New Sesquiterpenoids from the Algal-Derived Fungus Penicillium chermesinum EN-480
title_full_unstemmed Three New Sesquiterpenoids from the Algal-Derived Fungus Penicillium chermesinum EN-480
title_short Three New Sesquiterpenoids from the Algal-Derived Fungus Penicillium chermesinum EN-480
title_sort three new sesquiterpenoids from the algal-derived fungus penicillium chermesinum en-480
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7230704/
https://www.ncbi.nlm.nih.gov/pubmed/32272624
http://dx.doi.org/10.3390/md18040194
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