Novel 4-Thiazolidinone Derivatives as Anti-Infective Agents: Synthesis, Characterization, and Antimicrobial Evaluation
Table 2
Mean diameter of zone of inhibition (mm) of synthesized compounds (4a–4f), standard and control against various microorganisms.
S. number
Compounds
Conc. (μg/mL)
Gram +ve strains
Gram –ve strains
Fungal strains
SA
BS
BP
ML
PA
PF
EC
AN
PC
1
(4a-C18H18FN3OS)
50 100 200 400 800 1600
8 9 10 10 11 14
10 11 11 12 13 14
8 9 12 16 18 20
10 10 12 13 14 14
8 10 13 14 16 18
14 14 16 17 18 19
8 10 12 13 13 14
8 10 11 12 13 14
9 10 11 13 15 17
2
(4b-C22H21N3OS)
50 100 200 400 800 1600
8 13 14 15 16 18
12 13 15 16 17 19
13 14 15 17 18 20
15 16 17 18 19 21
12 13 14 15 17 19
12 13 15 16 17 19
8 12 14 15 16 18
12 14 16 17 18 19
12 13 14 15 17 18
3
(4c-C19H21N3O2S)
50 100 200 400 800 1600
8 8 8 8 10 12
8 8 12 14 15 16
8 10 14 16 18 20
8 8 10 13 14 14
9 12 13 14 15 16
10 12 14 15 16 18
10 10 13 14 14 15
8 8 10 12 13 14
10 11 13 15 16 17
4
(4d-C18H19N3O2S)
50 100 200 400 800 1600
8 13 15 17 19 21
13 14 15 17 18 19
12 13 14 16 17 18
14 16 17 18 19 20
15 16 17 18 19 20
13 14 15 16 17 19
12 13 15 16 18 20
8 12 13 14 16 18
8 12 14 16 17 19
5
(4e-C16H17N3O2S)
50 100 200 400 800 1600
12 13 14 15 16 17
14 15 16 20 21 24
12 13 15 16 18 19
13 15 16 17 19 20
8 13 14 15 17 19
8 13 14 16 17 18
8 13 14 15 17 19
8 13 14 15 17 18
12 13 14 16 17 19
6
(4f-C14H15N3OS2)
50 100 200 400 800 1600
8 9 10 12 13 15
9 10 12 14 16 18
8 8 10 12 18 21
8 8 8 10 12 14
10 12 16 18 20 21
10 14 16 17 18 19
8 10 12 14 14 16
8 8 10 12 14 17
8 10 12 13 15 18
7
Norfloxacin
10
25
22
30
24
26
25
27
—
—
8
Fluconazole
10
—
—
—
—
—
—
—
22
23
9
Control (10% DMSO)
—
—
—
—
—
—
—
—
—
—
BS: B. subtilis, SA: S. aureus, BP: B. pumilus, ML: M. luteus, PA: P. aeruginosa, EC: E. coli, PF: P. fluorescens, AN: A. niger, PC: P. chrysogenum, control = 10% v/v DMSO, and (—) = no activity.