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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