In vitro activity of WIN 51711, a new broad-spectrum antipicornavirus drug
Open Access
- 1 June 1985
- journal article
- research article
- Published by American Society for Microbiology in Antimicrobial Agents and Chemotherapy
- Vol. 27 (6), 883-886
- https://doi.org/10.1128/aac.27.6.883
Abstract
WIN 51711 (5-[7-[4-(4,5-dihydro-2-oxazolyl)phenoxy]heptyl]-3-methylisoxazole), a new antipicornavirus drug, is a potent inhibitor of human entero- and rhinoviruses at concentrations not inhibitory to HeLa cell growth. In plaque reduction assays, WIN 51711 reduced plaque formation by 9 enteroviruses and 33 rhinoviruses, with MICs of 0.004 to 0.17 and 0.004 to 6.2 micrograms/ml, respectively. Addition of WIN 51711 to infected cells at concentrations of 0.02 to 5.0 micrograms/ml reduced the yield of picornaviruses by 90%. Other RNA viruses (nonpicornaviruses) and DNA viruses were unaffected by the compound.This publication has 8 references indexed in Scilit:
- Enteroviruses and meningitisThe Pediatric Infectious Disease Journal, 1983
- Portraits of Viruses: the PicornavirusesIntervirology, 1983
- Prevention of human poliovirus-induced paralysis and death in mice by the novel antiviral agent arildoneAntimicrobial Agents and Chemotherapy, 1982
- Antiviral activity of arildone on deoxyribonucleic acid and ribonucleic acid virusesAntimicrobial Agents and Chemotherapy, 1980
- Inhibition of uncoating of poliovirus by arildone, a new antiviral drugVirology, 1979
- Preliminary Studies of the Mode of Action of Arildone, a Novel Antiviral AgentAntimicrobial Agents and Chemotherapy, 1979
- Antiviral activity of some .beta.-diketones. 1. Aryl alkyl diketones. In vitro activity against both RNA and DNA virusesJournal of Medicinal Chemistry, 1977
- Plaque Assay of Herpesvirus Hominis on Human Embryonic FibroblastsExperimental Biology and Medicine, 1969