Akanthopyrones A-D, α-Pyrones Bearing a 4-O-Methyl-β-d-glucopyranose Moiety from the Spider-Associated Ascomycete Akanthomyces novoguineensis.

Molecules 2017 Jul 18;22(7). Epub 2017 Jul 18.

Department of Microbial Drugs, Helmholtz Centre for Infection Research, 38124 Braunschweig, Germany.

Hypocrealean fungi have proved to be prolific bioactive metabolite producers; they have caught the attention of mycologists throughout the world. However, only a few studies on the insect and spider parasitic genus have so far been carried out. In this study, we report the isolation, structural elucidation and biological activities of four unprecedented glycosylated α-pyrone derivatives, akanthopyrones A-D (-), from a culture of collected in Thailand. The chemical structures of the akanthopyrones were determined by extensive 1D- and 2D-NMR, and HRMS spectroscopic analysis. Their absolute configurations were determined. Akanthopyrone A () exhibited weak antimicrobial activity against DSM10 and cytotoxicity against the HeLa cell line KB-3-1, while akanthopyrone D () showed weak activity against MUCL 29892.

Download full-text PDF

Source
http://dx.doi.org/10.3390/molecules22071202DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6152309PMC
July 2017
33 Reads

Publication Analysis

Top Keywords

akanthopyrones a-d
8
collected thailand
4
culture collected
4
derivatives akanthopyrones
4
thailand chemical
4
a-d culture
4
structures akanthopyrones
4
extensive 1d-
4
determined extensive
4
akanthopyrones determined
4
α-pyrone derivatives
4
chemical structures
4
glycosylated α-pyrone
4
report isolation
4
study report
4
carried study
4
genus carried
4
isolation structural
4
structural elucidation
4
unprecedented glycosylated
4

Similar Publications