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. 2013 Feb;57(2):804–810. doi: 10.1128/AAC.02052-12

Table 1.

Binding to and inhibition of HCV NS5B GT 1b-con-1 polymerase by GS-9669 and other reference NNIs

Compound Avg wild-type KD (nM) ± SDa M423T KD fold shiftb Mean wild-type IC50 (nM) ± SDc M423T IC50 fold shiftd
GS-9669 1.35 ± 0.49 10.5 40 ± 17 4
Lomibuvir 2.21 ± 0.66 10.3 55 ± 17 4
Filibuvir 31.5 ± 14.4 950 73 ± 4 >94
a

Average kinetic parameters across three surfaces extracted by using a global fit of a 1:1 binding model.

b

Ratio of mutant KD (equilibrium dissociation constant) over wild-type KD values.

c

Arithmetic mean of data from at least two experiments.

d

Ratio of mutant IC50 over wild-type IC50 values.