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PMID: 167186 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

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

Journal of virology ·Vol. 15 ·No. 5 ·1975-05-00 ·Pages 1284-5

Cheng YC, Goz B, Neenan JP, Ward DC, Prusoff WH

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.

MeSH Terms
Amines/pharmacology,toxicity Antiviral Agents/pharmacology DNA, Viral/biosynthesis Idoxuridine/analogs & derivatives,pharmacology,toxicity Simplexvirus/analysis,drug effects,growth & development Virus Replication
Chemicals
Amines Antiviral Agents DNA, Viral Idoxuridine
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Cheng Y C
Goz B
Neenan J P
Ward D C
Prusoff W H
References (2)
2 references, click to expand
  1. Acquisition of thymidine kinase activity by herpes simplex-infected mouse fibroblast cells.
    Biochem Biophys Res Commun. 1963 Apr 2;11:55-9 PMID: 14033128
  2. Pharmacology of viruses.
    Annu Rev Pharmacol. 1970;10:143-70 PMID: 4986558
Article Info
Journal
Journal of virology
Abbr.
J Virol
ISSN
0022-538X
Published
1975-05-00
Pages
1284-5
Language
English
Region
United States
NLM ID
0113724
PMCID
PMC354587
Subset
IM
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