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Table 3 IC50 (μg/ml) of the compounds 3–19

From: Design, synthesis, in vitro anticancer, molecular docking and SAR studies of new series of pyrrolo[2,3-d]pyrimidine derivatives

Compound

MCF7

A549

HCT116

PC3

HePG2

PACA2

3a

–

–

44.5 ± 1.3

–

19.2 ± 0.6

–

3b

–

–

–

–

–

69.7 ± 1.3

4a

32.4 ± 0.8

68.9 ± 0.5

–

–

–

24.1 ± 1.0

4b

45.8 ± 1.0

17.5 ± 0.4

58.4 ± 0.7

28.5 ± 0.8

84.3 ± 0.7

–

5

–

–

–

–

–

–

6

15.2 ± 0.9

–

31.2 ± 0.9

31.1 ± 0.9

 

40 ± 1.0

7

16.2 ± 1.6

–

–

–

–

–

8

48.0 ± 1.5

–

68.1 ± 1.0

–

17.8 ± 1.3

23.5 ± 0.6

9a

–

–

–

–

–

–

9b

–

–

–

–

–

–

10

61.1 ± 1.4

–

26.9 ± 0.6

11.6 ± 0.8

–

–

11a

–

–

–

–

–

55.4 ± 1.4

11b

48.4 ± 0.8

–

–

27.7 ± 0.1

–

–

12

11.9 ± 0.9

–

–

–

–

59.7 ± 0.7

13

–

–

–

–

–

–

14a

1.7 ± 0.4

–

–

–

37.9 ± 0.9

–

14b

16.8 ± 0.9

–

–

18.7 ± 0.2

17.5 ± 0.8

–

15

42.8 ± 0.6

54.0 ± 1.7

–

–

29.1 ± 0.5

–

16a

–

–

–

–

–

–

16b

5.7 ± 0.9

–

–

–

–

–

17

–

34.1 ± 1.5

37.8 ± 0.4

66.8 ± 2.0

8.7 ± 0.8

6.4 ± 0.7

18a

–

–

–

–

–

–

18b

3.4 ± 0.3

–

–

19.2 ± 0.9

28.1 ± 0.4

15 ± 0.9

19

–

–

–

–

19.4 ± 0.8

–

Dox

26.1 ± 0.1

28.3 ± 1.3

37.6 ± 0.8

23.8 ± 0.2

21.6 ± 0.8

28.3 ± 0.4