Table 1 Antibacterial activity of synthesized compounds

From: Chiral dependence of multifunctional supramolecular materials in crop protection

Compounds

Inhibition ratio (%)

Regression equation

R2

EC50a (μg·mL-1)

100 μg·mL-1

50 μg·mL-1

AIM-10S

100

100

y = 13.507x + 0.3806

0.9386

2.20 ± 0.02

AIM-10R

100

100

y = 23.852x − 0.5440

0.9711

1.71 ± 0.01

AIM-12S

100

100

y = 6.9179x + 4.0826

0.9733

1.36 ± 0.03

AIM-12R

100

100

y = 12.354x + 3.8282

0.9999

1.24 ± 0.07

AIM-14S

100

100

y = 16.760x + 1.9238

0.9821

1.53 ± 0.01

AIM-14R

100

100

y = 14.738x + 2.7247

0.9757

1.43 ± 0.02

AIM-16S

0

0

/

/

>100

AIM-16R

100

100

y = 10.276x − 6.9906

0.9946

14.68 ± 0.03

AIM-18S

0

0

/

/

>100

AIM-18R

0

0

/

/

>100

AIM-12S@β-CD

100

100

y = 8.5075x + 4.9695

0.9428

1.01 ± 0.05

AIM-12R@β-CD

100

100

y = 7.1056x + 5.6470

0.9623

0.81 ± 0.02

β-CD

0

0

/

/

>100

KSMb

80.18 ± 1.69

55.72 ± 5.88

y = 2.1312x + 1.5648

0.9968

40.91 ± 2.06

TCb

67.11 ± 2.38

/

y = 5.9455x + 6.4599

0.9992

84.62 ± 2.10

  1. Compounds AIM-10S/R to AIM-18S/R were assessed for their inhibitory efficacy against Xoo at 50 and 100 μg·mL⁻¹, with corresponding EC50 values determined.
  2. Note: aEC50 values are indicated as means ± SD (standard deviation); bCommercialized bactericide as the positive control. KSM kasugamycin, TC thiodiazole-copper.