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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...

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Autores principales: Yi, Xue-Wen, He, Juan, Sun, Li-Tang, Liu, Ji-Kai, Wang, Guo-Kai, Feng, Tao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
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.
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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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