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. 2015 Aug 14;59(9):5814–5818. doi: 10.1128/AAC.00534-15

TABLE 1.

Antiviral activities of SG85 and rupintrivir against 14 RV and 4 enteroviruses in virus-cell-based assays

Virus strain Median EC50 (μM) ± MADa
SG85 Rupintrivir
RV-A
    RV02 0.14 ± 0.03a 0.010 ± 0.006a
    RV09 0.032 ± 0.008a 0.011 ± 0.001a
    RV15 0.031 ± 0.004a 0.013 ± 0.001a
    RV29 0.04 ± 0.03a 0.008 ± 0.002a
    RV41 0.038 ± 0.007a 0.0036 ± 0.0008a
    RV59 0.04 ± 0.02a 0.0102 ± 0.0001a
    RV63 0.01 ± 0.01a 0.0106 ± 0.0009a
    RV85 0.15 ± 0.02a 0.015 ± 0.008a
    RV89 0.05 ± 0.06a 0.0040 ± 0.0002a
RV-B
    RV14 0.055 ± 0.008a 0.018 ± 0.002a
    RV42 0.02 ± 0.02a 0.0026 ± 0.0008a
    RV70 0.05 ± 0.05a 0.0111 ± 0.0001a
    RV72 0.008 ± 0.005a 0.00356 ± 0.0001a
    RV86 0.02 ± 0.02a 0.0096 ± 0.0008a
EV-A EV71 0.10 ± 0.04a 0.004 ± 0.002a
EV-B CVB3 0.5 ± 0.1a 0.25 ± 0.04a
EV-B ECHO11 33 ± 7a 2.8 ± 0.7a
EV-C PV1 39 ± 18 8.2 ± 2.7a
a

Antiviral activity was determined in a CPE reduction assay with a 3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium readout. The results shown are from dose-response curves set up from four or more experiments of which at least two were independent. MAD, median absolute deviation.

b

One hundred percent inhibition of a virus-induced CPE can be achieved with this compound (as determined by microscopic inspection).