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Susceptibility of VV Δ F2L-gfp to selected thymidine analogs and cidofovir.
| Compound Name | VV Δ F2L-gfp (EC50, μM)a | VV WR wt (EC50, μM) |
| IDU | 2.5 ± 0.9 | 2.4 ± 0.6 |
| N-MCT | 6.2 ± 3.5 | 12 ± 1.6 |
| PFT3 | 2.0 ± 0.6 | 2.4 ± 0.4 |
| PFT4 | 2.3 ± 1.1 | 2.5 ± 0.1 |
| CDV | 11 ± 4.2 | 10 ± 0.3 |
a. Concentration required to reduce plaque formation by 50%. Values shown are the average of duplicate determinations with the standard deviations shown.
