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. 2013 May 28;8(5):e64010. doi: 10.1371/journal.pone.0064010

Table 3. Anti-HSV type-1 and HSV type-2 activity (EC50) of LabyA1.

Virus strain EC50 (µM)a
LabyA1 Cidofovir Acyclovir
HSV-1 wild-type KOS (reference strain) 0.56±0.05 0.48±0.11 0.18±0.09
RV-174 (clinical isolate) 2.7±1.0 1.3±0.1 0.31±0.02
RV-175 (clinical isolate) 2.8±0.5 1.1±0.1 0.18±0.03
C559142 (clinical isolate) 0.45±0.02 0.53±0.09 0.09±0.02
Median EC50 1.6 µM 0.82 µM 0.18 µM
HSV-1 TK−b RV-294 (clinical isolate) 0.31±0.00 0.30±0.02 25±0.0
RV-179 (clinical isolate) 1.9±0.3 0.39±0.12 89±0.0
RV-117 (clinical isolate) 1.9±0.6 0.50±0.12 >79
Median EC50 1.9 µM 0.39 µM >79 µM
HSV-2 wild-type G (reference strain) 0.32±0.05 0.60±0.10 0.27±0.01
RV-124 (clinical isolate) 1.4±0.4 1.3±0.3 0.40±0.06
RV-24 (clinical isolate) 0.41±0.28 1.1±0.3 0.13±0.09
Median EC50 0.41 µM 1.1 µM 0.27 µM
HSV-2 TK−b RV-129 (clinical isolate) 0.32±0.19 0.55±0.20 74±12
BA19026589 (clinical isolate) 0.29±0.10 0.95±0.24 29±9
Median EC50 0.31 µM 0.75 µM 52 µM
a

EC50, 50% effective concentration or compound concentration required to reduce virus-induced cytopathicity (CPE) by 50%. Mean EC50± SEM up to 3 independent experiments are shown. Cidofovir and acyclovir are used as reference compound.

b

TK: thymidine kinase-deficient HSV strains (resistant to acyclovir, see [32] for more detail).