Table 1 The EC₅₀ values of target compounds against R. solani^A

BTL-1

H

y = 1.4403x + 3.3581

0.9932

13.8 i,j

BTL-2

4-F

y = 1.2104x + 3.6327

0.9630

13.4 j

BTL-3

4-Cl

y = 1.3063x + 3.8144

0.9856

7.3 p

BTL-4

4-Br

y = 1.2214x + 3.6116

0.9832

13.7 i,j

BTL-5

4-CH₃

y = 1.1803x + 3.2980

0.9966

27.6 e

BTL-6

4-OCH₃

y = 0.9718x + 3.7821

0.9646

17.9 h

BTL-7

5-F

y = 2.4766x + 3.9060

0.9951

2.7 r

BTL-8

5-Cl

y = 2.7841x + 2.6106

0.9671

7.2 p

BTL-9

5-Br

y = 1.3326x + 3.8441

0.9921

9.8 n

BTL-10

6-F

y = 1.1538x + 3.7625

0.9981

11.8 k,l

BTL-11

6-Cl

y = 0.7749x + 4.8997

0.9869

1.3 s

BTL-11@NSCS NPs

–

y = 0.4459x + 5.0719

0.9982

0.7 s

BTL-12

6-Br

y = 1.4780x + 3.6367

0.9801

8.3 o

BTL-13

6-NO₂

y = 1.1031x + 3.5184

0.9849

22.0 g

BTL-14

6-CH₃

y = 1.2208x + 3.6662

0.9966

12.3 k

BTL-15

6-CF₃

y = 1.1606x + 3.8543

0.9940

9.7 n

BTL-16

6-OCH₃

y = 0.9079x + 3.6190

0.9944

33.1 d

BTL-17

6-OCF₃

y = 1.4334x + 3.5432

0.9527

10.3 m,n

BTL-18

6-COCH₂CH₃

y = 1.0012x + 3.5904

0.9657

25.5 f

BTL-19

6-COOCH₃

y = 1.2274x + 3.2635

0.9671

25.9 f

BTL-20

6-OH

–

–

 > 100 a

BTL-21

6-SOOCH₃

y = 1.0350 x + 3.8088

0.9655

14.1 i

BTL-22

4,6-di-F

y = 0.8438x + 4.3754

0.9728

5.4 q

BTL-23

4,6-di-Cl

y = 2.4080x + 4.0733

0.9813

2.4 r

BTL-24

4,6-di-CH₃

y = 0.7123x + 3.6862

0.9950

69.9 c

Fluopyram

–

y = 1.4736x + 2.1763

0.9508

82.4 b

Azoxystrobin

–

y = 0.7673x + 4.1994

0.9735

11.1 l,m