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. 2006 Jul;50(7):2525–2529. doi: 10.1128/AAC.01489-05

TABLE 2.

Activities of alkoxyalkyl esters of CDV, cCDV, and HPMPA against VV and CPV in PHK monolayers

Compound VV
CPV
Cytotoxicity (μg/ml)
SIe
EC50 (μg/ml)a Fold decreaseb EC50 (μg/ml)a Fold decreaseb MCC (μg/ml)c CC50 (μg/ml)d VV CPV
HDP-CDV 0.48 ± 0.52 20 0.32 ± 0.19 30 20 0.18 ± 0.18 0.4 0.6
ODE-CDV 0.081 ± 0.079 130 0.053 ± 0.037 180 20 0.012 ± 0.011 0.2 0.3
OLP-CDV 0.40 ± 0.44 30 0.33 ± 0.23 30 20 0.034 ± 0.027 0.1 0.1
ODBG-CDV 0.058 ± 0.070 230 0.072 ± 0.071 170 >5 0.012 ± 0.011 0.2 0.2
OLE-CDV 0.065 ± 0.037 170 0.035 ± 0.022 290 >20 0.014 ± 0.013 0.2 0.4
CDV 5.8 ± 4.2 5.3 ± 2.1 >50 7.2 ± 6.7 1.2 1.4
OLE-cCDV 0.31 ± 0.32 110 0.12 ± 0.17 160 >20 0.055 ± 0.080 0.2 0.5
cCDV 18.9 ± 12.9 9.9 ± 5.7 >50 41.7 ± 34.9 2.2 4.2
HDP-HPMPA 0.079 ± 0.059 30 0.022 ± 0.023 50 2 0.021 ± 0.025 0.3 1.0
ODE-HPMPA 0.005 ± 0.000 560 0.0015 ± 0.0008 750 2 0.0078 ± 0.0110 2 5.2
HPMPA 1.5 ± 0.9 0.61 ± 0.28 20 0.53 ± 0.05 0.4 0.9
a

Concentration required to inhibit 50% of virus-induced CPE. The EC50 values of each compound represent the mean ± standard deviation of the EC50 values of at least two independent experiments.

b

Fold decrease in EC50 relative to that of the parental compound based on molar values, given the following molecular weights: HDP-CDV, 583.68; ODE-CDV, 581.71; OLP-CDV, 609.71; ODBG-CDV, 717.85; OLE-CDV, 595.68; CDV, 315.12; OLE-cCDV, 559.65; cCDV, 297.2; HDP-HPMPA, 585.72; ODE-HPMPA, 599.38; HPMPA, 325.

c

Minimum cytotoxic concentration required to alter cell morphology.

d

Concentration required to reduce cell growth by 50%. The CC50 values of each compound represent the mean ± standard deviation of the CC50 values of at least two independent experiments.

e

Selectivity index (ratio of CC50 to E50).