Abstract |
3'-Azido-2,6-diaminopurine-2',3'-dideoxyriboside ( AzddDAPR) is a potent and selective inhibitor of human immunodeficiency virus (HIV) replication in vitro. It also inhibits Moloney murine sarcoma virus (MSV)-induced transformation of murine C3H/3T3 embryo fibroblasts. AzddDAPR causes a marked dose-dependent suppression of MSV-induced tumor formation and mortality therewith associated in newborn mice infected with MSV. Combination of AzddDAPR with ribavirin resulted in a marked potentiation of its anti-retrovirus activity in vitro and a significant enhancement of its inhibitory effect on MSV-induced tumor formation in vivo. A slight increase in the in vivo toxicity of AzddDAPR was noted when combined with ribavirin.
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Authors | J Balzarini, P Herdewijn, E De Clercq |
Journal | Antiviral research
(Antiviral Res)
1989 May-Jun
Vol. 11
Issue 4
Pg. 161-71
ISSN: 0166-3542 [Print] Netherlands |
PMID | 2545163
(Publication Type: Journal Article)
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Chemical References |
- Antiviral Agents
- Dideoxynucleosides
- Ribonucleosides
- 3'-azido-2,6-diaminopurine-2',3'-dideoxyriboside
- Ribavirin
- Dideoxyadenosine
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Topics |
- Animals
- Antiviral Agents
(pharmacology)
- Cell Transformation, Neoplastic
- Cells, Cultured
- Dideoxyadenosine
(analogs & derivatives)
- Dideoxynucleosides
(pharmacology)
- Drug Synergism
- HIV
(drug effects, growth & development)
- Humans
- Mice
- Mice, Inbred Strains
- Moloney murine sarcoma virus
(drug effects, genetics, pathogenicity)
- Ribavirin
(pharmacology)
- Ribonucleosides
(pharmacology)
- Sarcoma Viruses, Murine
(drug effects)
- Sarcoma, Experimental
(pathology)
- Virus Replication
(drug effects)
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