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3-Decalinoyltetramic acids from kiwi-associated fungus Zopfiella sp. and their antibacterial activity against Pseudomonas syringae
Four rare 3-decalinoyltetramic acid derivatives, zofielliamides A–D (1–4), were obtained from cultures of kiwi-associated fungus Zopfiella sp. Their structures with absolute configurations were established by extensive spectroscopic methods and single crystal X-ray diffraction. The compounds possess...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Royal Society of Chemistry
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9033601/ https://www.ncbi.nlm.nih.gov/pubmed/35478665 http://dx.doi.org/10.1039/d1ra02120f |
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author | Yi, Xue-Wen He, Juan Sun, Li-Tang Liu, Ji-Kai Wang, Guo-Kai Feng, Tao |
author_facet | Yi, Xue-Wen He, Juan Sun, Li-Tang Liu, Ji-Kai Wang, Guo-Kai Feng, Tao |
author_sort | Yi, Xue-Wen |
collection | PubMed |
description | Four rare 3-decalinoyltetramic acid derivatives, zofielliamides A–D (1–4), were obtained from cultures of kiwi-associated fungus Zopfiella sp. Their structures with absolute configurations were established by extensive spectroscopic methods and single crystal X-ray diffraction. The compounds possessed rare pentacyclic systems that might derive from a polyene precursor via [4 + 2] intramolecular Diels–Alder reactions. Compounds 1, 2, and 4 showed antibacterial activity against plant pathogen Pseudomonas syringae with MIC values of 64, 32, and 64 μg mL(−1), respectively. |
format | Online Article Text |
id | pubmed-9033601 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90336012022-04-26 3-Decalinoyltetramic acids from kiwi-associated fungus Zopfiella sp. and their antibacterial activity against Pseudomonas syringae Yi, Xue-Wen He, Juan Sun, Li-Tang Liu, Ji-Kai Wang, Guo-Kai Feng, Tao RSC Adv Chemistry Four rare 3-decalinoyltetramic acid derivatives, zofielliamides A–D (1–4), were obtained from cultures of kiwi-associated fungus Zopfiella sp. Their structures with absolute configurations were established by extensive spectroscopic methods and single crystal X-ray diffraction. The compounds possessed rare pentacyclic systems that might derive from a polyene precursor via [4 + 2] intramolecular Diels–Alder reactions. Compounds 1, 2, and 4 showed antibacterial activity against plant pathogen Pseudomonas syringae with MIC values of 64, 32, and 64 μg mL(−1), respectively. The Royal Society of Chemistry 2021-05-25 /pmc/articles/PMC9033601/ /pubmed/35478665 http://dx.doi.org/10.1039/d1ra02120f Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Yi, Xue-Wen He, Juan Sun, Li-Tang Liu, Ji-Kai Wang, Guo-Kai Feng, Tao 3-Decalinoyltetramic acids from kiwi-associated fungus Zopfiella sp. and their antibacterial activity against Pseudomonas syringae |
title | 3-Decalinoyltetramic acids from kiwi-associated fungus Zopfiella sp. and their antibacterial activity against Pseudomonas syringae |
title_full | 3-Decalinoyltetramic acids from kiwi-associated fungus Zopfiella sp. and their antibacterial activity against Pseudomonas syringae |
title_fullStr | 3-Decalinoyltetramic acids from kiwi-associated fungus Zopfiella sp. and their antibacterial activity against Pseudomonas syringae |
title_full_unstemmed | 3-Decalinoyltetramic acids from kiwi-associated fungus Zopfiella sp. and their antibacterial activity against Pseudomonas syringae |
title_short | 3-Decalinoyltetramic acids from kiwi-associated fungus Zopfiella sp. and their antibacterial activity against Pseudomonas syringae |
title_sort | 3-decalinoyltetramic acids from kiwi-associated fungus zopfiella sp. and their antibacterial activity against pseudomonas syringae |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9033601/ https://www.ncbi.nlm.nih.gov/pubmed/35478665 http://dx.doi.org/10.1039/d1ra02120f |
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