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. 2015 Jun 24;20(7):11660–11675. doi: 10.3390/molecules200711660

Table 1.

Antibacterial activities against Xanthomonas oryzae pv. oryzaeof the title compounds.

Compds. Toxic Regression Equation R EC50 (μg/mL)
2-(Methylsulfonyl)-5-phenyl-1,3,4-oxadiazole y = 2.16x + 2.18 0.98 20.07 ± 1.21
2-(Ethylsulfonyl)-5-phenyl-1,3,4-oxadiazole y = 1.52x + 2.77 0.98 29.00 ± 1.25
2-(Methylsulfonyl)-5-(4-fluorophenyl)-1,3,4-oxadiazole y = 4.13x + 0.89 0.95 9.89 ± 1.52
2-(Ethylsulfonyl)-5-(4-fluorophenyl)-1,3,4-oxadiazole y = 3.28x + 1.61 0.96 10.80 ± 1.43
2-(Methylsulfonyl)-5-(4-chlorophenyl)-1,3,4-oxadiazole y = 1.72x + 2.64 0.99 23.21 ± 0.98
2-(Ethylsulfonyl)-5-(4-chlorophenyl)-1,3,4-oxadiazole y = 1.60x + 2.25 0.99 52.61 ± 1.08
2-(Methylsulfonyl)-5-(2,4-dichlorophenyl)-1,3,4-oxadiazole y = 1.04x + 3.21 0.99 52.14 ± 1.05
2-(Ethylsulfonyl)-5-(2,4-dichlorophenyl)-1,3,4-oxadiazole y = 1.43x + 2.42 0.97 63.95 ± 1.05
Bismerthiazole y = 1.50x + 2.05 0.98 92.61 ± 2.15
Thiodiazole copper y = 1.54x + 1.79 0.98 121.82 ± 3.59