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. 2019 Aug 23;63(9):e00889-19. doi: 10.1128/AAC.00889-19

TABLE 1.

Cytotoxicity and anti-YFV activity of nucleoside analogs

Compound Huh-7 cells
RD cells
Virus CPE inhibition in RD cells (%)
CC50a (μM) MNTCa (μM) CC50a (μM) MNTCa (μM)
1 >100 >20 56 >20 44.7 ± 0.4
2 81 >20 94 >20 54.3 ± 0.4
3 60 >20 >100 >20 26 ± 1.1
4 >100 >20 30.9 >20 99.5 ± 0.3
5 >100 >20 >100 >20 <2
6 >100 >20 >100 >20 <5
7 >100 >20 >100 >20 <2
8 37 >20 80 >20 <2
9 >100 >20 >100 >20 95 ± 1
10 70 >20 >100 >20 99.5 ± 0.3
11 22 15 >100 >20 99.9 ± 0.1
12 >100 >20 >100 >20 <5
13 17 >10 77 >20 99 ± 0.4
14 10 5 11 7 99.8 ± 0.1d
15 7 5 12 7.5 99.9 ± 0.1d
16b >100 >20 >100 >20 98 ± 0.7
17 2.9 2 10.5 6.5 99.5 ± 0.8c
18 11.5 5.5 32.5 16 90.5 ± 1d
19 >100 >20 >100 >20 <5
20 62 >20 >100 >20 <2
21 >100 >20 >100 >20 99 ± 0.2
a

Cytotoxicity of all nucleoside analogs was measured using MTS assay to calculate the CC50 and maximum nontoxic concentration (MNTC) of each compound.

b

Sofosbuvir (positive control).

c

Compound 17 was tested at 1.5 μM for its anti-YFV activity because of its MNTC.

d

Compounds 14, 15, and 18 were tested in 5 μM for their anti-YFV activity because of their MNTCs. All other compounds were tested in 20 μM against YFV in a CPE inhibition assay using MTS assay.