Table 2.
Concentration–responses of aristolactam derivatives on cytotoxicity and anti-HIV activity.
Compound | IC50 (μmol/L)a | CC50 (μmol/L)b | SIc |
---|---|---|---|
1 | 0.69 ± 0.09 | 6.88 ± 0.31 | 9.94 |
2 | 1.03 ± 0.38 | 16.91 ± 3.22 | 16.45 |
3 | 3.73 ± 1.00 | 17.15 ± 0.34 | 4.59 |
4 | 3.07 ± 0.22 | 6.98 ± 0.09 | 2.27 |
5 | 1.07 ± 0.06 | 4.51 ± 0.96 | 4.23 |
6 | 1.06 ± 0.03 | 4.97 ± 0.62 | 4.70 |
7 | 2.00 ± 0.61 | 3.62 ± 0.15 | 1.80 |
8 | 0.55 ± 0.01 | 3.72 ± 0.01 | 6.74 |
9 | 0.44 ± 0.01 | 3.64 ± 0.08 | 8.31 |
Seliciclib | 2.29 ± 0.40 | 25.49 ± 0.17 | 11.11 |
The inhibitory effects on HIV-1 infection and cell viability were determined in TZM-bl cells infected with HIV-1NL4-3 at an MOI of 1.
aIC50: half-maximal inhibitory concentration.
bCC50: concentration that reduces cell viability by 50%.
cSI: selectivity index, i.e. the ratio of IC50 to CC50.