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Table 18 (a) IC50 of the titled compounds (29a-j) against of MCF-7 and CaCo-2 cell line—benzo [d] imidazole pyrimidine derivatives; (b) IC50 of the titled compounds (30a-j) against of MCF-7 and CaCo-2 cell line—benzo [d] imidazole pyrazole derivatives Rajendran et al. [38]

From: Synthesis and therapeutic potential of imidazole containing compounds

Compounds

Substituent R

Substituent R1

Molecular formula

IC50 ± SD (µM)

MCF-7

CaCo-2

(a)

29a

H

C17H13N5

8.22 ± 1.48

5.67 ± 1.25

29b

H

C16H12N6

10.43 ± 1.45

9.56 ± 1.33

29c

H

C19H17N5O2

 > 30

28.40 ± 2.48

29d

H

C18H14ClN5O

13.05 ± 2.07

12.33 ± 1.80

29e

H

C25H17N5

 > 30 ± 2.87

 > 30 ± 2.98

29f

CH3

C18H15N5

 > 30 ± 2.66

 > 30 ± 2.43

29 g

CH3

C17H14N6

18.56 ± 2.82

16.23 ± 1.24

29 h

CH3

C19H16ClN5O

 > 30 ± 2.19

25.50 ± 2.74

29i

CH3

C20H19N5O2

25.11 ± 2.44

21.89 ± 2.35

29j

CH3

C26H19N5

 > 30 ± 2.80

 > 30 ± 2.06

Fluorouracil

   

7.26 ± 2.30

5.23 ± 2.36

(b)

30a

H

C22H16N4

22.65 ± 2.32

28.45 ± 2.59

30b

H

C21H15N5

12.79 ± 2.20

9.788 ± 1.48

30c

H

C23H17ClN4O

 > 30 ± 2.86

 > 30 ± 2.48

30d

H

C24H20N4O2

15.34 ± 2.67

13.27 ± 1.56

30e

H

C30H20N4

 > 30 ± 2.52

 > 30 ± 2.33

30f

CH3

C23H18N4

 > 30 ± 2.41

 > 30 ± 2.69

30g

CH3

C22H17N5

19.04 ± 2.56

17.32 ± 2.27

30h

CH3

C24H19ClN4O

 > 30 ± 2.38

29.76 ± 2.64

30i

CH3

C25H22N4O2

21.73 ± 2.46

18.35 ± 2.54

30j

CH3

C31H22N4

 > 30 ± 2.58

 > 30 ± 2.62

Fluorouracil

   

7.26 ± 2.30

5.23 ± 2.36