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Ganoaustralins A and B, Unusual Aromatic Triterpenes from the Mushroom Ganoderma australe

Two triterpenes, ganoaustralins A (1) and B (2), featuring unprecedented 6/6/6/5/6 scaffolds were isolated from the fruiting bodies of the mushroom Ganoderma australe. The structures were determined by extensive NMR and HRESIMS spectroscopic analysis. The absolute configuration of the C-25 in ganoau...

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Autores principales: Zhou, Lin, Chen, He-Ping, Li, Xinyang, Liu, Ji-Kai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9785556/
https://www.ncbi.nlm.nih.gov/pubmed/36558971
http://dx.doi.org/10.3390/ph15121520
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author Zhou, Lin
Chen, He-Ping
Li, Xinyang
Liu, Ji-Kai
author_facet Zhou, Lin
Chen, He-Ping
Li, Xinyang
Liu, Ji-Kai
author_sort Zhou, Lin
collection PubMed
description Two triterpenes, ganoaustralins A (1) and B (2), featuring unprecedented 6/6/6/5/6 scaffolds were isolated from the fruiting bodies of the mushroom Ganoderma australe. The structures were determined by extensive NMR and HRESIMS spectroscopic analysis. The absolute configuration of the C-25 in ganoaustralin A was assigned by the phenylglycine methyl ester (PGME) method. The relative and absolute configurations of the polycyclic backbones were determined by NMR and ECD calculations, respectively. The plausible biosynthetic pathways of ganoaustralins A and B were proposed. Ganoaustralin B showed weak inhibition against β-secretase 1.
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spelling pubmed-97855562022-12-24 Ganoaustralins A and B, Unusual Aromatic Triterpenes from the Mushroom Ganoderma australe Zhou, Lin Chen, He-Ping Li, Xinyang Liu, Ji-Kai Pharmaceuticals (Basel) Article Two triterpenes, ganoaustralins A (1) and B (2), featuring unprecedented 6/6/6/5/6 scaffolds were isolated from the fruiting bodies of the mushroom Ganoderma australe. The structures were determined by extensive NMR and HRESIMS spectroscopic analysis. The absolute configuration of the C-25 in ganoaustralin A was assigned by the phenylglycine methyl ester (PGME) method. The relative and absolute configurations of the polycyclic backbones were determined by NMR and ECD calculations, respectively. The plausible biosynthetic pathways of ganoaustralins A and B were proposed. Ganoaustralin B showed weak inhibition against β-secretase 1. MDPI 2022-12-06 /pmc/articles/PMC9785556/ /pubmed/36558971 http://dx.doi.org/10.3390/ph15121520 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Zhou, Lin
Chen, He-Ping
Li, Xinyang
Liu, Ji-Kai
Ganoaustralins A and B, Unusual Aromatic Triterpenes from the Mushroom Ganoderma australe
title Ganoaustralins A and B, Unusual Aromatic Triterpenes from the Mushroom Ganoderma australe
title_full Ganoaustralins A and B, Unusual Aromatic Triterpenes from the Mushroom Ganoderma australe
title_fullStr Ganoaustralins A and B, Unusual Aromatic Triterpenes from the Mushroom Ganoderma australe
title_full_unstemmed Ganoaustralins A and B, Unusual Aromatic Triterpenes from the Mushroom Ganoderma australe
title_short Ganoaustralins A and B, Unusual Aromatic Triterpenes from the Mushroom Ganoderma australe
title_sort ganoaustralins a and b, unusual aromatic triterpenes from the mushroom ganoderma australe
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9785556/
https://www.ncbi.nlm.nih.gov/pubmed/36558971
http://dx.doi.org/10.3390/ph15121520
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