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Fusarisolins A–E, Polyketides from the Marine-Derived Fungus Fusarium solani H918

Five new (fusarisolins A–E, 1 to 5) and three known (6 to 8) polyketides were isolated from the marine-derived fungus Fusarium solani H918, along with six known phenolics (9 to 14). Their structures were established by comprehensive spectroscopic data analyses, methoxyphenylacetic acid (MPA) method,...

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Detalles Bibliográficos
Autores principales: Niu, Siwen, Tang, Xi-Xiang, Fan, Zuowang, Xia, Jin-Mei, Xie, Chun-Lan, Yang, Xian-Wen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6410219/
https://www.ncbi.nlm.nih.gov/pubmed/30791608
http://dx.doi.org/10.3390/md17020125
Descripción
Sumario:Five new (fusarisolins A–E, 1 to 5) and three known (6 to 8) polyketides were isolated from the marine-derived fungus Fusarium solani H918, along with six known phenolics (9 to 14). Their structures were established by comprehensive spectroscopic data analyses, methoxyphenylacetic acid (MPA) method, chemical conversion, and by comparison with data reported in the literature. Compounds 1 and 2 are the first two naturally occurring 21 carbons polyketides featuring a rare β- and γ-lactone unit, respectively. All isolates (1 to 14) were evaluated for their inhibitory effects against tea pathogenic fungus Pestalotiopsis theae and 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) synthase gene expression. Compound 8 showed potent antifungal activity with an ED(50) value of 55 μM, while 1, 8, 13, and 14 significantly inhibited HMG-CoA synthase gene expression.