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Table 4 Antibacterial activity of synthesized compounds (3a–k and 3l–p) against Gram positive and Gram negative bacteria

From: Palladium(0) catalyzed Suzuki cross-coupling reaction of 2,5-dibromo-3-methylthiophene: selectivity, characterization, DFT studies and their biological evaluations

Entry

Product no

% inhibition (50 μg/ml)

P. aeruginosa

B. subtilis

E. coli

S. aureus

S. typhi

1

3a

67.3 ± 0.76

***

94.5 ± 0.09

33.9 ± 0.37

27.6 ± 0.08

2

3b

39.2 ± 0.45

***

50.1 ± 0.29

9.57 ± 0.15

5.58 ± 0.05

3

3c

***

***

***

***

***

4

3d

34.9 ± 0.27

***

7.8 ± 0.09

***

8.34 ± 0.23

5

3e

***

***

***

***

**

6

3f

***

***

***

***

***

7

3g

***

***

***

***

***

8

3h

37.6 ± 0.26

***

50.4 ± 0.45

***

12.0 ± 0.02

9

3i

41.1 ± 0.47

***

70.4 ± 0.78

***

2.59 ± 0.01

10

3j

***

***

***

***

***

11

3k

50.5 ± 0.58

***

72.5 ± 0.87

20.1 ± 0.06

17.3 ± 0.05

12

3 l

***

***

***

***

***

13

3m

***

***

***

***

***

14

3n

20.8 ± 0.17

***

30.6 ± 0.26

***

*

15

3o

***

***

***

***

***

16

3p

***

***

***

***

***

17

Control

100 ± 1.28

100 ± 1.21

100 ± 1.01

100 ± 0.99

100 ± 0.99

  1. *** Showed no activity. The results are average ± SD of triplicate experiments p < 0.05. Streptomycin was used as control standard drug