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Table 1 Antifungal activity of the title compounds 7a-7s at 50 mg/L

From: Synthesis and antifungal activity of novel pyrazolecarboxamide derivatives containing a hydrazone moiety

Compound

Inhibition ratea (%)

G. zeae

F. oxysporum

C. mandshurica

7a

40.82 ± 0.88

8.05 ± 1.61

16.11 ± 1.09

7b

39.87 ± 0.92

10.40 ± 3.34

15.44 ± 1.54

7c

31.96 ± 1.59

12.75 ± 1.48

12.75 ± 1.39

7d

33.23 ± 1.0

33.22 ± 1.99

16.78 ± 1.43

7e

35.76 ± 2.32

34.56 ± 3.11

19.46 ± 1.58

7f

47.78 ± 1.54

10.07 ± 2.92

12.75 ± 1.39

7g

50.32 ± 2.57

8.72 ± 1.45

7.38 ± 1.19

7h

40.82 ± 0.88

5.03 ± 1.22

16.11 ± 1.21

7i

49.05 ± 3.02

27.85 ± 1.62

37.25 ± 1.40

7j

48.73 ± 2.74

11.41 ± 1.32

20.13 ± 1.24

7k

37.66 ± 1.78

15.10 ± 2.03

8.39 ± 1.17

7l

40.19 ± 2.05

8.39 ± 1.54

16.11 ± 1.21

7m

29.11 ± 1.38

13.42 ± 1.43

12.08 ± 1.18

7n

36.39 ± 2.64

14.09 ± 1.40

15.10 ± 1.57

7o

36.08 ± 1.58

5.03 ± 1.40

14.09 ± 1.20

7p

37.34 ± 1.13

11.07 ± 1.45

11.07 ± 1.26

7q

45.89 ± 3.91

9.73 ± 1.25

16.44 ± 1.06

7r

6.65 ± 2.98

10.40 ± 1.47

22.48 ± 1.68

7s

39.24 ± 1.43

5.03 ± 1.31

11.07 ± 1.15

Carbendazimb

100.00 ± 3.74

100 ± 10.90

100 ± 8.76

  1. aAverage of three replicates, bThe commercial agricultural fungicide carbendazim was used for the comparison of activity.