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. 1975 May;15(5):1284–1285. doi: 10.1128/jvi.15.5.1284-1285.1975

Selective inhibition of herpes simplex virus by 5-amino-2,5-dideoxy-5-iodouridine.

Y C Cheng, B Goz, J P Neenan, D C Ward, W H Prusoff
PMCID: PMC354587  PMID: 167186

Abstract

5-Amino-2,5-dideoxy-5-iodouridine, a nel thymidine analogue, is a potent inhibitor of herpes simplex virus type 1 replication. In contrast to most other nucleoside analogues which possess antiviral activity, 5-amino-2,5-dideoxy-5-iodouridine exhibits little, if any, cellular toxicity. Preliminary evidence suggests that 5-amino-2,5-dideoxy-5-iodouridine selectively inhibits viral-specific DNA synthesis.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Goz B., Prusoff W. H. Pharmacology of viruses. Annu Rev Pharmacol. 1970;10:143–170. doi: 10.1146/annurev.pa.10.040170.001043. [DOI] [PubMed] [Google Scholar]
  2. KIT S., DUBBS D. R. Acquisition of thymidine kinase activity by herpes simplex-infected mouse fibroblast cells. Biochem Biophys Res Commun. 1963 Apr 2;11:55–59. doi: 10.1016/0006-291x(63)90027-5. [DOI] [PubMed] [Google Scholar]

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