Table 2: Cytotoxicity of 1,3-diphenylpyrazole-chromenoquinolin-6-one compounds (5a‒ad) on selected human cancer cell lines.

 

Compound

 

 

 

 

 

IC50 values (µM) a

 

 

 

 

 

 

 

A549b

 

 

MCF-7c

 

 

HeLad

 

 

DU-145e

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

5a

21.26 ± 1.08

 

9.91 ± 0.55

 

22.38 ± 1.55

 

18.32 ± 0.88

 

 

 

5b

26.91 ± 1.92

 

8.20 ± 0.42

 

22.96 ± 1.32

 

17.51 ± 0.92

 

 

 

5c

32.35 ± 1.86

 

10.73± 0.34

 

39.90 ± 2.22

 

21.85 ± 0.86

 

 

 

5d

50.11 ± 2.78

 

15.27 ± 0.46

 

62.57 ± 3.96

 

30.85 ± 1.78

 

 

 

5e

6.46 ± 0.99

 

5.46 ± 0.51

 

14.79 ± 2.02

 

6.31 ± 0.99

 

 

 

5f

10.81 ± 0.63

 

1.98 ± 0.71

 

3.23 ± 0.22

 

4.69 ± 0.63

 

 

 

5g

11.32 ± 0.89

 

3.68 ± 0.91

 

14.12 ± 1.02

 

6.53 ± 0.89

 

 

 

5h

25.50 ± 1.54

 

11.70 ± 0.61

 

25.11 ± 1.86

 

18.01 ± 1.54

 

 

 

5i

19.66 ± 0.98

 

5.02 ± 0.71

 

18.38 ± 1.04

 

10.78 ± 0.98

 

 

 

5j

15.55 ± 1.52

 

1.82 ± 0.24

 

4.68 ± 0.31

 

6.84 ± 0.52

 

 

 

5k

15.24 ± 1.26

 

4.68 ± 0.46

 

18.72 ± 1.02

 

9.14± 1.26

 

 

 

5l

16.98 ± 0.52

 

3.65 ± 0.23

 

15.70 ± 1.03

 

6.61 ± 0.52

 

 

 

5m

16.73 ± 1.06

 

3.50 ± 0.96

 

7.24 ± 0.98

 

10.47 ± 1.86

 

 

 

5n

39.81 ± 2.05

 

12.56 ± 1.66

 

19.67 ±1.96

 

21.92 ± 1.26

 

 

 

5o

24.83 ± 1.52

 

17.17 ± 1.03

 

19.61 ± 2.02

 

20.18 ± 0.64

 

 

 

5p

14.21 ± 1.29

 

11.81 ± 0.94

 

21.72 ± 1.03

 

11.22 ± 1.69

 

 

 

5q

13.30 ± 1.38

 

2.75 ± 0.54

 

4.26 ± 0.76

 

6.18 ± 0.96

 

 

 

5r

15.88 ± 1.62

 

2.80 ± 0.84

 

4.36 ± 0.12

 

6.92 ± 0.47

 

 

 

5s

10.59 ± 0.43

 

1.22 ± 0.94

 

3.51 ± 0.13

 

2.99 ± 0.13

 

 

 

5t

5.25 ± 0.23

 

1.64 ± 0.76

 

2.71 ± 0.33

 

4.52 ± 0.37

 

 

 

5u

19.05 ± 2.69

 

11.41 ± 0.52

 

17.37 ± 0.02

 

13.58 ± 2.69

 

 

 

5v

17.11 ± 1.36

 

3.23 ± 0.98

 

10.56 ± 0.41

 

7.49 ± 0.76

 

 

 

5w

21.00 ± 1.65

 

9.75 ± 0.33

 

16.18 ± 0.66

 

15.89 ± 1.65

 

 

 

5x

15.88 ± 1.20

 

2.81 ± 0.87

 

4.36 ± 0.53

 

6.92 ± 0.60

 

 

 

5y

11.35 ± 1.23

 

9.53 ± 0.91

 

23.77± 1.89

 

10.30 ± 1.23

 

 

 

5z

26.30 ± 2.36

 

13.92 ± 0.78

 

24.85 ± 2.49

 

19.56 ± 1.36

 

 

 

5aa

28.84 ± 2.13

 

20.14 ± 1.02

 

26.91 ± 1.26

 

22.40 ± 1.73

 

 

 

5ab

17.37 ± 0.95

 

12.73 ± 0.51

 

16.87 ± 1.23

 

14.12 ± 0.61

 

 

 

5ac

17.78 ± 1.05

 

13.66 ± 1.56

 

21.18 ± 2.01

 

17.00 ± 1.05

 

 

 

5ad

20.41 ± 0.92

 

12.30 ± 1.32

 

20.46 ± 1.36

 

18.31 ± 0.76

 

 

 

Doxorubicin

1.24 ± 0.59

 

1.32 ± 0.11

 

1.53 ± 0.47

 

2.11 ± 0.70

 

 

 

(Positive control)

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

a 50% Inhibitory concentration after 48 h of drug treatment and the values are average of three individual experiments; bHuman lung cancer; cHuman breast cancer; dHuman cervical cancer; dHuman prostate cancer.