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Table 3 In vitro antifungal activity of compounds 3 and 4

From: A facile iodine(III)-mediated synthesis of 3-(3-aryl-1-phenyl-1H-pyrazol-4-yl)-[1,2,4]triazolo[4,3-a]pyridines via oxidation of 2-((3-aryl-1-phenyl-1H-pyrazol-4-yl)methylene)-1-(pyridin-2-yl)hydrazines and their antimicrobial evaluations

Compounds

Mycelial growth of inhibition (%)

 

Aspergillus niger

Aspergillus flavus

3a

52.5

51.1

3b

51.1

50.6

3c

52.5

51.1

3d

50.0

49.8

3e

44.4

45.5

3f

45.5

44.4

3g

47.7

45.5

4a

66.5

58.8

4b

62.3

62.5

4c

60.5

60.6

4d

52.5

51.1

4e

48.8

50.0

4f

69.5

68.5

4g

51.1

50.0

Fluconazole

81.1

77.7