Table 3. Antiviral Evaluation of Series 2 against EV-D68a in RD Cellsb.
compound | R2 | EC50 (μM)b | CC50 (μM)c | SId |
---|---|---|---|---|
19 | CF3 | 0.05 ± 0.01 | >2.5 | >50 |
20 | CH3 | 0.28 ± 0.03 | >2.5 | >9 |
21 | C2H5 | 0.10 ± 0.007 | >2.5 | >25 |
22 | n-C3H7 | 0.41 ± 0.03 | >0.8 | >2 |
23 | i-C3H7 | 0.40 ± 0.37 | >0.8 | >2 |
24 | n-C4H9 | 0.71 ± 0.05 | >2.5 | >3 |
25 | t-C4H9 | 4.22 ± 0.12 | >7.4 | >2 |
EV-D68 strain: STL-2014-12.
EC50: concentration that effectively inhibited the cytopathic effect by 50% in Rhabdomyosarcoma cell lines (RD cells).
CC50: concentration that inhibited the normal uninfected cell viability by 50%, or the maximum soluble concentration which started from 200 μM in serial 3-fold dilutions.
Selectivity index (SI) calculated as CC50/EC50 ratio.