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. 2006 Sep 30;15(1):227–234. doi: 10.1016/j.bmc.2006.09.066

Table 1.

Antiviral activities of the final compounds 14 against HIV type 1 and 2, EMCV, Cox. B3, VSV, and HSV type 1 and 2a

Compound MT4b CS50c HIV (EC50)
HeLaf CC50g Anti-RNA (EC50)
Verok CC50 Anti-HSV (EC50)
IIIBd RODe EMCVh Cox.B3i VSVj HSV-1l HSV-2m
1 >100 >100 >100 >100 >100 >100 >100 >100 >100 >100
2 >100 >100 >100 >100 >100 >100 >100 >100 >100 >100
3 >100 >100 >100 14.54 >14.54 >14.54 9.43 >100 >100 >100
4 >100 >100 >100 >100 >100 >100 >100 >100 >100 >100
Ribavirin >300 23.45 64.09 10.32
ddI >100 6.62 16.00 >10 0.17 0.47
a

The potency is given as an EC50 (50% effective concentration, μg/mL) and evaluated by the degree of inhibition of virus-induced cytopathogenic effects (CPE).

b

HTLV-1-infected human T-lymphocyte.

c

50% cytostatic concentration.

d

Human immunodeficiency virus type 1 strain IIIB.

e

Human immunodeficiency virus type 1 strain ROD.

f

Human cervical carcinoma cell.

g

50% cytotoxic concentration.

h

Encephalomyocarditis virus.

i

Coxsackie B virus type 3.

j

Vesicular stomatitis virus.

k

African Green monkey kidney cell.

l

Herpes simplex virus type 1.

m

Herpes simplex virus type 2.