Viral polymerase inhibitors T-705 and T-1105 are potential inhibitors of Zika virus replication

Arch Virol. 2017 Sep;162(9):2847-2853. doi: 10.1007/s00705-017-3436-8. Epub 2017 Jun 8.

Abstract

Since 2015, 69 countries and territories have reported evidence of vector-borne Zika virus (ZIKV) transmission. Currently, there are no effective licensed vaccines or drugs available for the treatment or prevention of ZIKV infection. We tested a series of compounds for their ability to inhibit ZIKV replication in cell culture. The compounds in T-705 (favipiravir) and T-1105 were found to have antiviral activity, suggesting that these compounds are promising candidates for further development as specific antiviral drugs against ZIKV.

Keywords: Broad-spectrum antiviral drugs; T-1105; T-705; Zika virus (ZIKV).

MeSH terms

  • Amides / chemical synthesis
  • Amides / chemistry
  • Amides / pharmacology*
  • Animals
  • Antiviral Agents / pharmacology
  • Cell Survival / drug effects
  • Chlorocebus aethiops
  • Dose-Response Relationship, Drug
  • Molecular Structure
  • Pyrazines / chemical synthesis
  • Pyrazines / chemistry
  • Pyrazines / pharmacology*
  • Vero Cells
  • Virus Replication / drug effects*
  • Zika Virus / drug effects*
  • Zika Virus / physiology

Substances

  • Amides
  • Antiviral Agents
  • Pyrazines
  • T 1105
  • favipiravir