Effects of Introduction of Hydrophobic Group on Ribavirin Base on Mutation Induction and Anti-RNA Viral Activity

This publication has 24 references indexed in Scilit:

• Ribavirin and lethal mutagenesis of poliovirus: molecular mechanisms, resistance and biological implications
  Virus Research, 2005
• The Predominant Mechanism by Which Ribavirin Exerts Its Antiviral Activity In Vitro against Flaviviruses and Paramyxoviruses Is Mediated by Inhibition of IMP Dehydrogenase
  Journal of Virology, 2005
• Ribavirin suppresses eIF4E-mediated oncogenic transformation by physical mimicry of the 7-methyl guanosine mRNA cap
  Proceedings of the National Academy of Sciences, 2004
• An unnatural hydrophobic base, 4-propynylpyrrole-2-carbaldehyde, as an efficient pairing partner of 9-methylimidazo[(4,5)- b ]pyridine
  Bioorganic & Medicinal Chemistry Letters, 2003
• RNA virus error catastrophe: Direct molecular test by using ribavirin
  Proceedings of the National Academy of Sciences, 2001
• The broad-spectrum antiviral ribonucleoside ribavirin is an RNA virus mutagen
  Nature Medicine, 2000
• Effects of selenazofurin and ribavirin and their 5'-triphosphates on replicative functions of influenza A and B viruses
  Antimicrobial Agents and Chemotherapy, 1986
• Mechanism of Action of 1-β-D-Ribofuranosyl-1,2,4-Triazole-3-Carboxamide (Virazole), A New Broad-Spectrum Antiviral Agent
  Proceedings of the National Academy of Sciences, 1973
• Design, synthesis, and broad spectrum antiviral activity of 1-.beta.-D-ribofuranosyl-1,2,4-triazole-3-carboxamide and related nucleosides
  Journal of Medicinal Chemistry, 1972
• Broad-Spectrum Antiviral Activity of Virazole: 1-β-D-Ribofuranosyl-1,2,4-triazole-3-carboxamide
  Science, 1972