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Table 3 Antimicrobial and anticancer screening results of synthesized thiazole molecules (p1–p10)

From: 4-(4-Bromophenyl)-thiazol-2-amine derivatives: synthesis, biological activity and molecular docking study with ADME profile

Compound

(Antimicrobial screening) MIC = µM

aIC50 = µM

Microbial species

Bacterial

Fungal

Cancer cell line

S.A.

B.S.

E.C.

C.A.

A.N.

MCF7

p1

31

62.0

31

31

31

17.4

p2

16.1

32.1

16.1

32.1

32.1

10.5

p3

32.4

32.4

32.4

32.4

16.2

37.4

p4

28.8

28.8

28.8

28.8

28.8

38.0

p5

29.6

29.6

29.6

29.6

29.6

40.3

p6

30.5

30.5

30.5

15.3

30.5

73.3

p7

33.1

33.1

33.1

16.5

33.1

47.6

p8

31

31.0

62.0

15.5

62.0

52.1

p9

33.5

67.0

67.0

33.5

33.5

17.2

p10

17.4

34.8

34.8

34.8

34.8

21.4

Norfloxacin

4.7

4.7

4.7

–

–

–

Fluconazole

–

–

–

5.0

5.0

–

5-Fluorouracil

–

–

–

–

–

5.2

  1. S.A.: Staphylococcus aureus (MTCC3160); B.S.: Bacillus subtilis (MTCC441); E.C.: Escherichia coli (MTCC443); C.A.: Candida albicans (MTCC227) and A.N.: Aspergillus niger (MTCC281)
  2. aIC50 is the concentration required to inhibit 50% of cell growth