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. 2015 Jan 29;20(2):2296–2309. doi: 10.3390/molecules20022296

Table 1.

Physical data, AChE and BChE inhibitory activities of 4aj.

Entry Comp 4 R Yield (%) a mp °C AChE Inhibition IC50 µM (±SD) BChE Inhibition IC50 µM (±SD)
1 a H 85 134–135 11.29 ± 0.21 15.73 ± 0.22
2 b 2-CH3 87 141–142 10.15 ± 0.17 21.32 ± 0.19
3 c 2-OCH3 82 126–127 12.23 ± 0.19 11.39 ± 0.12
4 d 2-Cl 85 136–137 15.17 ± 0.22 9.63 ± 0.15
5 e 3-OCH3 84 127–128 2.13 ± 0.11 17.44 ± 0.23
6 f 3-O2N 89 133–134 1.57 ± 0.09 15.32 ± 0.18
7 g 4-CH3 92 138–139 7.11 ± 0.13 10.46 ± 0.24
8 h 4-OCH3 80 129–130 3.67 ± 0.15 14.69 ± 0.17
9 i 4-Cl 88 132–133 5.83 ± 0.20 16.11 ± 0.15
10 j 2,4-Cl2 90 135–136 6.72 ± 0.18 12.79 ± 0.25
11 Galantamine - - - 2.09 ± 0.07 19.21 ± 0.12
12 Donepezil - - - 0.21 ± 0.02 3.6 ± 0.11

a Isolated yield.