From neuraminidase inhibitors to conjugates: a step towards better anti-influenza drugs?

Future Med Chem. 2014 May;6(7):757-74. doi: 10.4155/fmc.14.30.

Abstract

For the treatment of seasonal flu and possible pandemic infections the development of new anti-influenza drugs that have good bioavailability against a broad spectrum of influenza viruses including the resistant strains is needed. In this review, we summarize previous methods for the structural modification of zanamivir, a potent neuraminidase inhibitor that has rare drug resistance, in order to develop effective anti-influenza drugs. We also report recent research into the design of multivalent zanamivir drugs and bifunctional zanamivir conjugates, some of which have shown better efficacy in animal experiments. As a step towards developing improved antivirals, conjugating anti-influenza drugs with anti-inflammatory agents can improve oral bioavailability and also exert synergistic effect in influenza therapy.

Publication types

  • Review

MeSH terms

  • Animals
  • Antiviral Agents / chemistry*
  • Antiviral Agents / pharmacology
  • Drug Design*
  • Enzyme Inhibitors / chemistry
  • Enzyme Inhibitors / pharmacology
  • Humans
  • Influenza, Human / drug therapy*
  • Influenza, Human / enzymology
  • Influenza, Human / virology
  • Molecular Targeted Therapy
  • Neuraminidase / antagonists & inhibitors*
  • Neuraminidase / chemistry
  • Neuraminidase / metabolism
  • Orthomyxoviridae / drug effects
  • Orthomyxoviridae / enzymology*
  • Orthomyxoviridae / physiology
  • Orthomyxoviridae Infections / drug therapy*
  • Orthomyxoviridae Infections / enzymology
  • Orthomyxoviridae Infections / virology
  • Zanamivir / analogs & derivatives*
  • Zanamivir / pharmacology

Substances

  • Antiviral Agents
  • Enzyme Inhibitors
  • Neuraminidase
  • Zanamivir