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Pardinumones A–D: Antibacterial Polyketide–Amino Acid Derivatives from the Mushroom Tricholoma pardinum

[Image: see text] Four polyketide–amino acid derivatives, pardinumones A–D (1–4), were isolated from the wild mushroom Tricholoma pardinum. Their structures together with absolute configurations were characterized by means of spectroscopic data analyses, as well as calculated electronic circular dic...

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Autores principales: Yang, Hui-Xiang, Ma, Jin-Tao, He, Juan, Li, Zheng-Hui, Huang, Rong, Feng, Tao, Liu, Ji-Kai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8482770/
https://www.ncbi.nlm.nih.gov/pubmed/34604687
http://dx.doi.org/10.1021/acsomega.1c04418
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author Yang, Hui-Xiang
Ma, Jin-Tao
He, Juan
Li, Zheng-Hui
Huang, Rong
Feng, Tao
Liu, Ji-Kai
author_facet Yang, Hui-Xiang
Ma, Jin-Tao
He, Juan
Li, Zheng-Hui
Huang, Rong
Feng, Tao
Liu, Ji-Kai
author_sort Yang, Hui-Xiang
collection PubMed
description [Image: see text] Four polyketide–amino acid derivatives, pardinumones A–D (1–4), were isolated from the wild mushroom Tricholoma pardinum. Their structures together with absolute configurations were characterized by means of spectroscopic data analyses, as well as calculated electronic circular dichroism (ECD) and NMR with sorted training set (STS) protocol analysis. Compounds 1–4 exhibited antibacterial activity against Staphylococcus aureus, Staphylococcus epidermidis, and Escherichia coli with MIC values in the range of 6.25–50 μg/mL.
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spelling pubmed-84827702021-10-01 Pardinumones A–D: Antibacterial Polyketide–Amino Acid Derivatives from the Mushroom Tricholoma pardinum Yang, Hui-Xiang Ma, Jin-Tao He, Juan Li, Zheng-Hui Huang, Rong Feng, Tao Liu, Ji-Kai ACS Omega [Image: see text] Four polyketide–amino acid derivatives, pardinumones A–D (1–4), were isolated from the wild mushroom Tricholoma pardinum. Their structures together with absolute configurations were characterized by means of spectroscopic data analyses, as well as calculated electronic circular dichroism (ECD) and NMR with sorted training set (STS) protocol analysis. Compounds 1–4 exhibited antibacterial activity against Staphylococcus aureus, Staphylococcus epidermidis, and Escherichia coli with MIC values in the range of 6.25–50 μg/mL. American Chemical Society 2021-09-15 /pmc/articles/PMC8482770/ /pubmed/34604687 http://dx.doi.org/10.1021/acsomega.1c04418 Text en © 2021 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Yang, Hui-Xiang
Ma, Jin-Tao
He, Juan
Li, Zheng-Hui
Huang, Rong
Feng, Tao
Liu, Ji-Kai
Pardinumones A–D: Antibacterial Polyketide–Amino Acid Derivatives from the Mushroom Tricholoma pardinum
title Pardinumones A–D: Antibacterial Polyketide–Amino Acid Derivatives from the Mushroom Tricholoma pardinum
title_full Pardinumones A–D: Antibacterial Polyketide–Amino Acid Derivatives from the Mushroom Tricholoma pardinum
title_fullStr Pardinumones A–D: Antibacterial Polyketide–Amino Acid Derivatives from the Mushroom Tricholoma pardinum
title_full_unstemmed Pardinumones A–D: Antibacterial Polyketide–Amino Acid Derivatives from the Mushroom Tricholoma pardinum
title_short Pardinumones A–D: Antibacterial Polyketide–Amino Acid Derivatives from the Mushroom Tricholoma pardinum
title_sort pardinumones a–d: antibacterial polyketide–amino acid derivatives from the mushroom tricholoma pardinum
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8482770/
https://www.ncbi.nlm.nih.gov/pubmed/34604687
http://dx.doi.org/10.1021/acsomega.1c04418
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