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. 2021 Apr 15;220:113467. doi: 10.1016/j.ejmech.2021.113467

Table 1.

Cytotoxicity and antiviral activity of studied compounds against enveloped dsDNA viruses (M ± SD).

Cmpd EC50, μMa
CC50, μM
VZV, TK+ strain VZV, TK– strain CMV, AD-169 CMV,
Davis
HEL cells
11a 0.42 ± 0.08 (>238)b 15.9 ± 9.8 (>6) 54.69 (>2) 42.3 ± 3.4 (>2) >100
11b 0.200 ± 0.099 (>500) 11.3 ± 14.2 (>8) >100 >100 >100
11c 0.68 ± 0.11 (74) 15.2 ± 2.5 (3) >100 10.4 ± 0.8 (5) 50.3 ± 2.4
12a 8.7 ± 6.7 (>11) >100 >100 >100 >100
12b >20 >20 >100 >100 >100
12c 10.7 ± 1.3 (>9) 15.1 ± 7.0 (>6) >20 20 >100
12d >100 >100 >100 >100 >100
13 >100 >100 >100 >100 >100
14 >100 >100 >100 >100 >100
16a >100 >100 >100 >100 >100
16b >100 >100 >100 >100 >100
17 >100 >100 >100 >100 >100
18 >20 13.3 ± 0.9 (>8) >100 9.2 ± 1.7 (>11) >100
19 >100 >100 >100 >100 >100
20 >20 >20 48.9 (>2) 44.72 (>2) >100
23 >100 64.4 (>1.5) >20 >100 >100
Acyclovir 12.0 ± 9.7 56 ± 33 >300
Brivudine 0.034 ± 0.015 0.42 ± 0.26 >300
Ganciclovir 19 ± 14 1.79 ± 0.75 >300
Cidofovir 1.31 ± 0.1 0.61 ± 0.29 >300
a

Effective concentration required to reduce virus plaque formation by 50%.

b

Selectivity index (SI) is shown in brackets.