1987
Selective inhibitory effects of (S)-9-(3-hydroxy-2-phosphonyl-methoxypropyl)adenine and 1-(2'-deoxy-2'-fluoro-ß-D-arabinofuranosyl)-5-iodouracil on seal herpesvirus (Phocid herpesvirus 1) infection in vitro.
Publication
Publication
Antiviral Research , Volume 7 - Issue 4 p. 221- 226
From a selection of 25 antiviral compounds with specific anti-herpes activity or broad-spectrum antiviral properties, two compounds, namely (S)-9-(3-hydroxy-2-phosphonyl-methoxypropyl)adenine and 1-(2'-deoxy-2'-fluoro-beta-D-arabinofuranosyl)-5-iodouracil, appeared particularly effective in inhibiting the cytopathogenicity of seal herpesvirus (phocid herpesvirus 1).
Additional Metadata | |
---|---|
, , , , , , , , , , , , , , , , | |
doi.org/10.1016/0166-3542(87)90030-1, hdl.handle.net/1765/3318 | |
Antiviral Research | |
Organisation | Erasmus MC: University Medical Center Rotterdam |
Osterhaus, A., Groen, J., & de Clercq, E. (1987). Selective inhibitory effects of (S)-9-(3-hydroxy-2-phosphonyl-methoxypropyl)adenine and 1-(2'-deoxy-2'-fluoro-ß-D-arabinofuranosyl)-5-iodouracil on seal herpesvirus (Phocid herpesvirus 1) infection in vitro. Antiviral Research, 7(4), 221–226. doi:10.1016/0166-3542(87)90030-1 |