Helicase-primase inhibitors for herpes simplex virus: looking to the future of non-nucleoside inhibitors for treating herpes virus infections

Future Med Chem. 2014 Jan;6(1):45-55. doi: 10.4155/fmc.13.192.

Abstract

Helicase-primase inhibitors (HPIs) are the first new family of potent herpes virus (herpes simplex and varicella-zoster virus) inhibitors to go beyond the preliminary stages of investigation since the emergence of the original nucleoside analog inhibitors. To consider the clinical future of HPIs, this review puts the exciting new findings with two HPIs, amenamevir and pritelivir, into the historical context of antiviral development for the prevention and treatment of herpes simplex virus over the last century and, on this basis, the authors speculate on the potential evolution of these and other non-nucleoside inhibitors in the future.

Publication types

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

MeSH terms

  • Antiviral Agents / chemistry*
  • Antiviral Agents / pharmacology
  • Antiviral Agents / therapeutic use
  • DNA Helicases / antagonists & inhibitors*
  • DNA Helicases / genetics
  • DNA Helicases / metabolism
  • DNA Primase / antagonists & inhibitors*
  • DNA Primase / genetics
  • DNA Primase / metabolism
  • DNA Replication / drug effects
  • Herpes Simplex / drug therapy
  • Humans
  • Oxadiazoles / chemistry
  • Oxadiazoles / pharmacology
  • Oxadiazoles / therapeutic use
  • Pyridines / chemistry
  • Pyridines / pharmacology
  • Pyridines / therapeutic use
  • Simplexvirus / drug effects
  • Simplexvirus / enzymology*
  • Sulfonamides
  • Thiazoles / chemistry
  • Thiazoles / pharmacology
  • Thiazoles / therapeutic use
  • Viral Proteins / antagonists & inhibitors*
  • Viral Proteins / genetics
  • Viral Proteins / metabolism

Substances

  • ASP2151
  • Antiviral Agents
  • Oxadiazoles
  • Pyridines
  • Sulfonamides
  • Thiazoles
  • Viral Proteins
  • pritelivir
  • DNA Primase
  • DNA Helicases