Table II.
Antiviral activity in vitro | |||||
---|---|---|---|---|---|
Antiviral target | Synthetic compound | (µM) | Assay | HRV tested | Citation |
Capsid binder | Disoxaril | 0.01–18.1 | Plaque reduction assay | 35 serotypes | 139 |
Pleconaril | 0.03–17.5; seven completely resistant HRV‐B | Cell protection assay with crystal violet | All serotypes | 12 | |
Pirodavir | 0.003–39.0; four completely resistant HRV | Cell protection assay with MTT | All serotypes | 187 | |
Oxime ether 14 | 0.002–0.02 | Cell protection assay | 16 serotypes | 141 | |
Compound 19 | 0.01 | Cell protection assay with crystal violet | HRV‐2 | 188 | |
SCH 38057 | 20.4–29.2 | Plaque reduction assay | 6 serotypes | 191 | |
Ro 09‐0881 | 0.01–9.1 | Plaque reduction assay | 12 serotypes | 193 | |
BW863C | 0.007 | Plaque reduction assay | HRV‐1B | 194 | |
Isoflavan | ∼0.48 | Plaque reduction assay | HRV‐1B | 137 | |
MDL 20,957 | 0.02 | Plaque reduction assay | 32 serotypes | 196 | |
MDL‐860 | 3.25a | Virus yield reduction assay | 90 serotypes | 198 | |
2A and 3C Proteinase | Homophthalimides | 4.2 | Virus yield reduction assay | HRV‐2 and HRV‐14 | 215 |
3C Proteinase | Rupintrivir | 0.003–0.08 | Cell protection assay with XTT | 48 serotypes | 227 |
Compound 1 | 0.014–0.12 | Cell protection assay with XTT | 35 serotypes | 231 | |
RNA synthesis | 2‐Furylmercury chloride | 0.02–2.5; 4 completely resistant HRV | Not described | 17 serotypes | 235 |
Ribavirin | 73.8 and 123.0 102.5 and 159.8 | Cell protection assay Plaque reduction assay | HRV‐2 and HRV‐14, resp. | 239 | |
Enviroxime | 0.17–1.0 | Plaque reduction assay | 15 serotypes | 244 | |
0.03–0.2 | Cell protection assay with crystal violet | 12 serotypes | 245 |
a1 µg/mL reduced the virus yield of 72 serotypes by at least 1.0 log10, 12 serotypes were intermediately inhibited, and 6 not.