Acyclic guanosine analogs as substrates for varicella-zoster virus thymidine kinase

Antimicrob Agents Chemother. 1986 Jan;29(1):171-4. doi: 10.1128/AAC.29.1.171.

Abstract

This study was performed to obtain information on the enzymatic background to the antiviral activity of acyclic guanosine analogs. Five acyclic guanosine analogs, the (R)- and (S)-enantiomers of 9-(3,4-dihydroxybutyl)guanine, 9-(4-hydroxybutyl)guanine, 9-[(2-hydroxyethoxy)methyl]guanine, and 9-[[2-hydroxy-1-(hydroxymethyl)ethoxy]methyl]guanine, were compared in enzyme kinetic experiments using purified varicella-zoster virus and human placenta mitochondrial thymidine kinase (TK). All analogs showed competitive patterns of inhibition in the phosphorylation of thymidine by varicella-zoster virus TK, but only low affinities and phosphorylation rates were observed. No affinity for the mitochondrial TK was observed for any of the analogs.

MeSH terms

  • Guanosine / analogs & derivatives*
  • Guanosine / metabolism
  • Herpesvirus 3, Human / drug effects
  • Herpesvirus 3, Human / enzymology*
  • Humans
  • Kinetics
  • Lung / metabolism
  • Mitochondria / enzymology
  • Phosphorylation
  • Thymidine Kinase / antagonists & inhibitors*
  • Virus Replication / drug effects

Substances

  • Guanosine
  • Thymidine Kinase