Caffeic acid derivatives: a new type of influenza neuraminidase inhibitors

Bioorg Med Chem Lett. 2013 Jun 15;23(12):3556-60. doi: 10.1016/j.bmcl.2013.04.033. Epub 2013 Apr 22.

Abstract

Recently, many natural products, especially some plant-derived polyphenols have been found to exert antiviral effects against influenza virus and show inhibitory activities on neuraminidases (NAs). In our research, we took caffeic acid which contained two phenolic hydroxyl groups as the basic fragment to build a small compound library with various structures. The enzyme inhibition result indicated that some compounds exhibited moderate activities against NA and compound 15d was the best with IC50=7.2 μM and 8.5 μM against N2 and N1 NAs, respectively. The 3,4-dihydroxyphenyl group from caffeic acid was important for the activity according to the docking analysis. Besides, compound 15d was found to be a non-competitive inhibitor with Ki=11.5±0.25 μM by the kinetic study and also presented anti-influenza virus activity in chicken embryo fibroblast cells. It seemed promising to discover more potent NA inhibitors from caffeic acid derivatives to cope with influenza virus.

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Caffeic Acids / chemistry*
  • Caffeic Acids / metabolism
  • Caffeic Acids / pharmacology*
  • Chick Embryo
  • Enzyme Inhibitors / chemistry*
  • Enzyme Inhibitors / pharmacology*
  • Fibroblasts / drug effects
  • Fibroblasts / virology
  • Humans
  • Influenza A Virus, H1N1 Subtype / enzymology*
  • Influenza A Virus, H5N1 Subtype / enzymology*
  • Kinetics
  • Models, Molecular
  • Neuraminidase / antagonists & inhibitors*
  • Neuraminidase / chemistry

Substances

  • Caffeic Acids
  • Enzyme Inhibitors
  • Neuraminidase
  • caffeic acid