Abstract |
A novel nucleoside analog, 8-chloro-7-deazaguanosine (8-Cl-7-dzGuo), was evaluated for anti-RNA virus activity in rodents in parallel with the related compound 7-deaza-7-thia-8-oxoguanosine (7-dzTOGuo). Half-daily intraperitoneal (i.p.) doses of each substance administered 24 and 18 h prior to i.p. virus challenge protected the majority of mice infected with banzi, encephalomyocarditis, San Angelo, and Semliki Forest viruses at doses of 25, 50 and 100 mg/kg/day. These compounds at 100 mg/kg/day also protected most suckling rats infected intranasally with rat coronavirus. However, no survival benefit was afforded to treated mice infected intranasally with vesicular stomatitis virus. 8-Cl-7-dzguo was orally active against Semliki Forest virus in mice at 200 and 400 mg/kg/day, whereas 7-dzTOGuo is reported to not be effective orally. In uninfected mice, the two compounds induced similar amounts of interferon following i.p. injections. Interferon was induced by oral treatments with 8-Cl-7-dzGuo but not with 7-dzTOGuo. Fifty percent acute lethal doses to uninfected mice treated i.p. in half-daily doses for one day with 7-deazaguanosine (7-dzGuo), 7-dzTOGuo, and 8-Cl-7-dzGuo were 400, 600 and > 1600 (no mortality at this dose) mg/kg/day, respectively. Daily, i.p. treatments for 14 days with these substances (100 mg/kg/day) showed 7-dzGuo as 100% lethal and the other two substances as not toxic. By virtue of reduced toxicity and oral bioavailability, 8-Cl-7-dzGuo appears to have the greatest clinical potential as an interferon-inducing antiviral agent.
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Authors | D F Smee, H A Alaghamandan, K Ramasamy, G R Revankar |
Journal | Antiviral research
(Antiviral Res)
Vol. 26
Issue 2
Pg. 203-9
(Mar 1995)
ISSN: 0166-3542 [Print] Netherlands |
PMID | 7605116
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- 8-chloro-7-deazaguanosine
- Antiviral Agents
- Guanosine
- isatoribine
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Topics |
- Animals
- Antiviral Agents
(pharmacology)
- Guanosine
(analogs & derivatives, pharmacology)
- Mice
- Molecular Structure
- RNA Viruses
(drug effects)
- Rats
- Virus Diseases
(drug therapy)
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