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. 2012 Oct;56(10):5387–5396. doi: 10.1128/AAC.01186-12

Table 1.

Potency of ASV and VX-950 against recombinant full-length HCV NS3/4A protease complexes representing different HCV genotypes

Genotype (strain) IC50 (nM)a
ASV VX-950b
1a (H77) 0.70 ± 0.06 12 ± 2
1b (J4L6S) 0.30 ± 0.02 22 ± 6
2a (HC-J6) 15 ± 1 95 ± 17
2b (HC-J8) 78 ± 2 12 ± 1
3a (S52) 320 ± 13 537 ± 4
4a (ED43) 1.6 ± 0.1 12 ± 1
5a (SA13) 1.7 ± 0.2 38 ± 3
6a (HK-6A) 0.9 ± 0.1 86 ± 2
a

Data are means ± standard deviations from at least three independent experiments.

b

VX-950 was preincubated with each of the respective NS3/4A protease complexes for 30 min before the addition of substrate to obtain optimum potency. Preincubation of ASV and enzyme was not required to enhance potency.