Table 2.
Cytotoxic effect of isocryptolepine derivatives [17].
No. | Substituent | IC50 μM | |||||
---|---|---|---|---|---|---|---|
R1 | R2 | R3 | BALB/3T3 | MV4-11 | A549 | HCT116 | |
10a | H | NH(CH2)3NH2 | H | 1.05 ± 0.13 | 0.12 ± 0.01 | 0.17 ± 0.05 | 0.26 ± 0.11 |
10b | OMe | NH(CH2)3NH2 | H | 0.31 ± 0.03 | 0.12 ± 0.05 | 0.16 ± 0.03 | 0.07 ± 0.03 |
10c | NO2 | NH(CH2)3NH2 | H | 0.36 ± 0.15 | 0.15 ± 0.06 | 0.35 ± 0.22 | 0.10 ± 0.02 |
10d | H | NH(CH2)3NH2 | Me | 0.95 ± 0.24 | 0.11 ± 0.04 | 0.18 ± 0.03 | 0.06 ± 0.02 |
10e | NO2 | NH(CH2)3NH2 | Me | 0.08 ± 0.02 | 0.05 ± 0.01 | 0.11 ± 0.07 | 0.01 ± 0.00 |
10f | H | NH(CH2)3NH(CH3)2 | H | 1.18 ± 0.20 | 0.41 ± 0.31 | 0.87 ± 0.27 | 0.55 ± 0.17 |
10g | Cl | NH(CH2)3NH(CH3)2 | Me | 0.82 ± 0.08 | 0.08 ± 0.03 | 0.57 ± 0.31 | 0.10 ± 0.02 |