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. 2012 Jan;56(1):271–279. doi: 10.1128/AAC.05636-11

Table 3.

Danoprevir potency against treatment-emergent NS3 substitutions

NS3 protease varianta EC50, nM (mean ± SD)b Fold changec
R155K 45.1 ± 30.8d 410
R155Q 6.3 ± 2.6e 57
D168E 3.2 ± 2.8d 29
D168V 10.4 ± 6.3d 93
D168T 33.0 ± 16.4d 300
I71V 0.06 ± 0.01d 0.57
V170I 0.12 ± 0.06d 1.05
Wild type 0.11 ± 0.05 N/A
a

Introduced as site-directed mutations (SDMs) into con1b HCV replicon genetic background if Con-1 sequence differed from identified substitution.

b

Data are from at least three independent experiments.

c

Fold change relative to parental Con-1 HCV replicon. N/A, not applicable.

d

Relative replication capacity of variant replicon is greater than 50% of wild type.

e

Relative replication capacity of R155Q variant is approximately 20% of wild type.