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. 2016 Sep 7;124:773–781. doi: 10.1016/j.ejmech.2016.09.014

Table 2.

Activity of compounds 4, 8, 15, 16, and 17a against cytomegalovirus (HCMV), herpes simplex virus-1 (HSV-1) and herpes simplex virus-1 (HSV-2) in human embryonic lung (HEL) cell cultures.

Comp. Antiviral activity EC50 (μM)a
Cytotoxicity (μM)
HMCV
HSV-1
HSV-2
MMCb
AD-169 Davis (KOS) TK KOS ACVr (G)
4a nd >100 >100 >100 >100 >100
4b >4 >4 >100 >100 >100 >100
4c nd >0.16 >100 >100 >100 4
4d nd >4 >20 >20 >20 20
8a nd >4 >20 >20 >20 20
8b nd >4 >4 >4 >4 20
8c nd >20 >100 >100 >100 100
15 >4 >4 >100 >100 >100 20
16a >4 >4 >100 >100 >100 >4
16b >20 >20 >20 >20 >20 100
16c >20 >20 >20 >20 >20 20
16d 76 100 >100 >100 >100 >100
17a >4 >4 >100 >100 >100 20
Ganciclovir 3.1 2.1 0.09 100 0.03 >100
Cidofovir 0.38 0.51 0.4 1.2 0.7 >250
Acyclovir 0.08 112 0.2 >250
Brivudin 0.007 50 96 >250
a

Effective concentration required to reduce virus plaque formation by 50%. Virus input was 20 plaque-forming units (PFU).

b

Maximum cytotoxic concentration that cause a microscopically detectable alteration of morphology.