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.
- 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]
- 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]