A Novel Ascochlorin Glycoside from the Insect Pathogenic Fungus Verticillium Hemipterigenum BCC 2370
Overview
Pharmacology
Authors
Affiliations
Vertihemipterin A, the ascochlorin glycoside, and its aglycone, 4',5'-dihydro-4'-hydroxyascochlorin, were isolated from the insect pathogenic fungus Verticillium hemipterigenum BCC 2370. A new analog, 8'-hydroxyascochlorin, and five known compounds, ascochlorin, LL-Z1272delta, 8',9'-dehydroascochlorin, ascofuranone and ascofuranol, were also isolated from the same fermentation broth. Structures of these compounds were elucidated by spectroscopic methods. Stereochemistry of the known compound, 4',5'-dihydro-4'-hydroxyascochlorin, was addressed by NMR spectral analyses and the modified Mosher's method. Antiviral (HSV-1) and cytotoxic activities of these ascochlorin analogs were evaluated.
Genome mining and biosynthetic pathways of marine-derived fungal bioactive natural products.
Han C, Song A, He Y, Yang L, Chen L, Dai W Front Microbiol. 2024; 15:1520446.
PMID: 39726967 PMC: 11669671. DOI: 10.3389/fmicb.2024.1520446.
Barilli E, Reveglia P, Agudo-Jurado F, Canete Garcia V, Cimmino A, Evidente A Toxins (Basel). 2023; 15(12).
PMID: 38133197 PMC: 10747461. DOI: 10.3390/toxins15120693.
Goncalves M, Hilario S, Van de Peer Y, Esteves A, Alves A J Fungi (Basel). 2022; 8(1).
PMID: 35049971 PMC: 8780691. DOI: 10.3390/jof8010031.
Bioactive Ascochlorin Analogues from the Marine-Derived Fungus .
Subko K, Kildgaard S, Vicente F, Reyes F, Genilloud O, Larsen T Mar Drugs. 2021; 19(2).
PMID: 33498522 PMC: 7909580. DOI: 10.3390/md19020046.
Complete biosynthetic pathways of ascofuranone and ascochlorin in .
Araki Y, Awakawa T, Matsuzaki M, Cho R, Matsuda Y, Hoshino S Proc Natl Acad Sci U S A. 2019; 116(17):8269-8274.
PMID: 30952781 PMC: 6486709. DOI: 10.1073/pnas.1819254116.