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. 2019 Dec 20;35(1):330–343. doi: 10.1080/14756366.2019.1699553

Table 1.

Structures, eeAChE and eqBChE inhibitory activities of target compounds.

Inline graphic
Compound R X Y AChEa (IC50c, μM or IRd, %) BChEb (IC50, μM or IR, %) SIe
9a H 3.14 ± 1.12 43.89 %
9b 2-CH3 8.08 ± 2.66 41.36 %
9c 3-CH3 3.83 ± 2.04 44.03 %
9d 4-CH3 25.71 ± 12.31 37.80 %
9e 3,4-CH3 9.97 ± 2.52 30.80 %
9f 3-OCH3 33.47 % 25.02 %
9g 4-OCH3 5.17 ± 2.25 41.46 %
9h 2-F 16.19 ± 4.34 30.01 %
9i 3-F 2.93 ± 1.96 95.07 ± 59.26 0.24
9j 4-F 4.70 ± 2.01 3.71 ± 1.88 1.27
9k 2-Cl 3.92 ± 1.20 46.48 %
9l 3-Cl 6.00 ± 3.31 36.93 %
9m 4-Cl 0.21 ± 0.03 49.93 %
9n 2-Br 8.87 ± 4.56 43.48 %
9o 3-Br 3.69 ± 1.83 42.83 %
9p 4-Br 11.06 ± 6.42 38.48 %
11a 4-OCH3 CH CH 38.08 ± 12.83 10.75 ± 5.55 3.54
11b 4-OCH3 N CH 48.57 % 44.57 %
11c 2-Cl N CH 5.44 ± 2.22 21.29 ± 5.00 0.26
11d 4-OCH3 CH N 18.81 % 16.51 %
11e 2-Cl CH N 7.48 ± 3.10 42.12 %
11f H N N 0.46 ± 0.40 43.07 %
15a H 0.38 ± 0.08 0.45 ± 0.02 0.84
15b 2-CH3 0.39 ± 0.11 0.66 ± 0.16 0.59
    1.49 ± 0.43f 1.33 ± 0.55g 1.12
15c 3-CH3 0.54 ± 0.14 0.47 ± 0.17 1.14
15d 4-CH3 24.77 ± 3.48 100.2 ± 22.09 0.24
15e 3-OCH3 9.35 ± 2.32 20.34 ± 3.08 0.45
15f 3-F 1.04 ± 0.48 1.37 ± 0.74 0.75
15g 3-Cl 0.15 ± 0.02 1.01 ± 0.46 0.15
15h 4-Cl 1.95 ± 0.28 2.23 ± 0.81 0.87
15i 2-Br 0.42 ± 0.06 0.22 ± 0.04 1.99
15j 3-Br 0.39 ± 0.15 0.16 ± 0.04 2.44
    1.25 ± 0.48f 0.66 ± 0.22g 1.89
Tacrine   0.02 ± 0.01 0.008 ± 0.004 2.50
Donepezil   0.009 ± 0.001 1.57 ± 0.35 0.006
a

AChE (EC 3.1.1.7) from electric eel.

b

BChE (EC 3.1.1.8) from horse serum.

c

Concentration required for 50% inhibition of ChEs, data were shown in mean ± SEM of triplicate independent experiments.

d

Inhibitory rate of the compounds under 100 μM on ChEs.

e

Selectivity index (SI)=AChE IC50/BChE IC50.

f

AChE (EC 3.1.1.7) from human.

g

BChE (EC 3.1.1.8) from human.