Table 2 Antixodant potencial of 12a–j.
Compounds | R | IC50 (µM) |
|---|---|---|
12a | Phenyl | 107.18 ± 3.49 |
12b | 2-Chlorophenyl | 105.93 ± 1.72 |
12c | 3-Chlorophenyl | 94.46 ± 4.61 |
12d | 4-Chlorophenyl | 116.15 ± 1.89 |
12e | 2,4-Dichorophenyl | 123.74 ± 1.01 |
12f | 4-Methoxyphenyl | 98.91 ± 4.83 |
12g | 4-Methylphenyl | 120.26 ± 3.91 |
12h | 2-Methyl phenyl | 130.53 ± 10.61 |
12i | 2,3-Dimethyl phenyl | 142.25 ± 1.39 |
12j | Ethyl phenyl | 102.36 ± 3.33 |
Quercetin[a] | – | 18.56 ± 2.19 |