Abstract
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.
Funder
National Natural Science Foundation of China
Fundamental Research Funds for the Central Universities, South-Central Minzu University
Natural Science Foundation of Hubei Province
Subject
Drug Discovery,Pharmaceutical Science,Molecular Medicine
Cited by
3 articles.
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