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. 2016 Mar 21;21(3):390. doi: 10.3390/molecules21030390

Table 1.

Average inhibition rates of compounds 46 and 7a7x against three phytopathogenic fungi.

Compounds Average Inhibition Rate ± SD (%)
No. R A. solani F. graminearum F. solani
4 - 61.2 ± 0.4 g 100.0 ± 0.0 a 53.4 ± 0.7 n
5 - 71.8 ± 0.5 b 77.7 ± 0.4 d 92.9 ± 0.1 a
6 - 2.0 ± 0.5 q 74.5 ± 0.5 e 57.9 ± 0.6 k
7a C6H5 53.1 ± 0.7 i 48.8 ± 0.4 j 41.7 ± 0.7 q
7b 2′-pyridyl 66.6 ± 0.0 de 47.0 ± 0.7 k 79.8 ± 0.5 d
7c 2′-CH3C6H4 2.7 ± 0.7 q 35.6 ± 0.4 n 65.3 ± 1.5 i
7d 3′-CH3C6H4 45.8 ± 0.9 k 43.6 ± 0.6 l 64.1 ± 0.4 j
7e 4′-CH3C6H4 28.7 ± 0.8 l 23.6 ± 0.2 q 77.0 ± 0.6 e
7f 2′-ClC6H4 2.1 ± 0.8 q 31.8 ± 0.4 p 68.1 ± 0.4 h
7g 3′-ClC6H4 21.4 ± 0.8 n 3.4 ± 0.3 s 86.1 ± 0.6 c
7h 4′-ClC6H4 5.7 ± 0.9 p 3.1 ± 0.6 s 72.2 ± 0.5 g
7i 2′,4′-Cl2C6H3 50.1 ± 0.8 j 7.1 ± 0.5 r 22.8 ± 0.6 u
7j 4′-CH3OC6H4 50.6 ± 0.3 j 6.3 ± 0.4 r 41.9 ± 0.3 q
7k 2′-FC6H4 68.4 ± 0.7 c 37.6 ± 0.5 m 40.5 ± 0.4 r
7l 3′-FC6H4 54.0 ± 0.9 i 33.0 ± 0.7 o 49.4 ± 0.2 p
7m 4′-FC6H4 58.9 ± 1.3 h 51.1 ± 0.6 h 52.1 ± 0.9 o
7n 2′-CF3C6H4 64.4 ± 0.9 f 80.5 ± 0.4 c 13.5 ± 1.0 w
7o 3′-CF3C6H4 25.7 ± 0.7 m 32.6 ± 0.8 po 54.6 ± 0.3 m
7p 4′-CF3C6H4 8.3 ± 0.3 o 80.1 ± 1.0 c 22.9 ± 0.4 u
7q 1′-naphthyl 65.1 ± 1.1 ef 49.9 ± 0.6 i 25.2 ± 0.7 t
7r 2′-naphthyl 25.8 ± 0.2 m 50.2 ± 0.6 hi 20.3 ± 0.1 v
7s CH3 68.4 ± 0.6 c 100.0 ± 0.0 a 86.0 ± 0.2 c
7t CH3CH2 59.1 ± 0.9 h 70.0 ± 0.3 f 80.1 ± 0.3 d
7u CH3(CH2)2 66.9 ± 0.9 cd 44.4 ± 0.7 l 69.2 ± 0.9 h
7v CH3(CH2)3 49.9 ± 0.8 j 85.4 ± 0.4 b 74.2 ± 0.2 f
7w CH3(CH2)4 66.5 ± 0.9 de 55.1 ± 0.2 g 56.6 ± 0.3 l
7x CH3(CH2)10 72.2 ± 0.2 b 85.6 ± 0.4 b 29.8 ± 0.4 s
TBZ - 89.1 ± 0.6 a 100.0 ± 0.0 a 89.3 ± 0.4 b

All values are expressed as means ± SD (n = 3). Tested fungi were treated with each compound at a concentration of 50 μg/mL for 72 h. The differences between data with the different lower case letters within a column are significant for the same tested fungus (p < 0.05).