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Table 1 Physical constants, antimycobacterial activity, and docking score of target compounds (4a–o)

From: Design and synthesis of new 3-((7-chloroquinolin-4-yl)amino)thiazolidin-4-one analogs as Mycobacterium tuberculosis DNA gyrase inhibitors

Code

Ar

M.P. (°C)

Yield (%)

MIC (μM)

Docking score

4a

4-Fluorobenzaldehyde

282

85

6.25

− 4.395

4b

2-Chlorobenzaldehyde

280

61

6.25

− 3.891

4c

4-Chlorobenzaldehyde

150

67

6.25

− 3.943

4d

2,3-Dichlorobenzaldehyde

300

73

12.5

− 3.223

4e

2,4-Dichlorobenzaldehyde

308

77

1.56

− 3.945

4f

4-Bromobenzaldehyde

140

81

3.12

− 4.291

4g

3-Bromo,4-fluorobenzaldehyde

294

66

1.56

− 3.771

4h

p-anisaldehyde

260

62

3.12

− 4.437

4i

3,4-Dimethoxybenzaldehyde

130

60

3.12

− 3.553

4j

3,4,5-Trimethoxybenzaldehyde

280

50

12.5

− 3.637

4k

4-Nitrobenzaldehyde

300

61

6.25

− 3.573

4l

4-Hydroxybenzaldehyde

312

62

12.5

− 4.533

4m

4-Cyanobenzaldehyde

304

58

12.5

− 4.439

4n

p-dimethylaminobenzaldehyde

195

60

1.56

− 3.14

4o

Thiophene-2-carbaldehyde

330

67

1.56

− 4.496

Ethambutol

1.56

− 6.245

Pyrazinamide

3.12

− 3.61

Ciprofloxacin

3.12

− 5.913