Mycobiology.  2014 Jun;42(2):189-192.

Neuraminidase Inhibitors from the Fermentation Broth of Phellinus linteus

Affiliations
  • 1Division of Biotechnology and Advanced Institute of Environment and Bioscience, Chonbuk National University, Iksan 570-752, Korea. bsyun@jbnu.ac.kr
  • 2Korea National College of Agriculture and Fisheries, Hwaseong 445-760, Korea.
  • 3Department of Beauty Science, Kwangju Women's University, Gwangju 506-713, Korea.

Abstract

During a search for neuraminidase inhibitors derived from medicinal fungi, we found that the fermentation broth of Phellinus linteus exhibited potent neuraminidase inhibitory activity. Through bioassay-guided fractionation, two active compounds were purified from the ethyl acetate-soluble portion of the fermentation broth of P. linteus. These structures were identified as inotilone (1) and 4-(3,4-dihydroxyphenyl)-3-buten-2-one (2) by spectroscopic methods. Compounds 1 and 2 inhibited H1N1 neuraminidase activity with IC50 values of 29.1 and 125.6 microM, respectively, in a dose-dependent manner. They also exhibited an antiviral effect in a viral cytopathic effect reduction assay using MDCK cells. These results suggest that compounds 1 and 2 from the culture broth of P. linteus would be good candidates for the prevention and therapeutic strategies towards viral infections.

Keyword

4-(3,4-Dihydroxyphenyl)-3-buten-2-one; Anti-influenza agent; Inotilone; Neuraminidase inhibitor; Phellinus linteus

MeSH Terms

Cytopathogenic Effect, Viral
Fermentation*
Fungi
Inhibitory Concentration 50
Madin Darby Canine Kidney Cells
Neuraminidase*
Neuraminidase
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