Table 1.
Structure and growth-inhibitory activity of ITC and related compounds against B. cereus.
# | Structure | MIC, μg ml−1
|
Synthetic protocol | |
---|---|---|---|---|
E. coli | B. cereus | |||
Aliphatic ITC derivatives | ||||
8. | CH3-NCS | >128 | 128 | * |
22. | CH2=CH-CH2 –NCS | >128 | 128 | * |
7. | CH3CH2CH2CH2-NCS | >128 | 128 | * |
Hydroxy- ITC derivatives | ||||
18. | HO -(CH2)4–NCS | >128 | 16 | * |
5. | HO -(CH2)5–NCS | >128 | 16 | * |
21. | HO -(CH2)6–NCS | >128 | 16 | * |
44. | HO -(CH2)7–NCS | >128 | 16 | * |
45. | HO -(CH2)8–NCS | >128 | 8 | I |
Charged ITC derivative | ||||
6. | −2O3PO -(CH2)5 -NCS | 128 | >128 | III |
Bifunctional ITC derivatives | ||||
38. | SCN -(CH2)4 –NCS | >64 | 2 | I |
39. | SCN -(CH2)5 –NCS | >64 | 2 | I |
40. | SCN -(CH2)6 –NCS | >64 | 2 | I |
41. | SCN -(CH2)7 -NCS | >64 | 2 | I |
42. | SCN -(CH2)8 -NCS | >64 | 2 | I |
43. | SCN-[(CH2)2 -O-]2 -(CH2)2 -NCS | >64 | 4 | I |
37. |
![]() |
8 | 0.5 | I |
16. |
![]() |
64 | 2 | I |
Aromatic and heterocyclic ITC derivatives | ||||
4. |
![]() |
>128 | >128 | * |
1. |
![]() |
64 | 16 | * |
17. |
![]() |
>128 | 16 | * |
3. |
![]() |
>128 | 64 | * |
2. |
![]() |
64 | 8 | * |
20. |
![]() |
128 | 8 | * |
27. |
![]() |
>128 | 16 | I |
19. |
![]() |
>128 | 8 | I |
34. |
![]() |
>128 | 8 | II |
29. |
![]() |
>128 | >128 | II |
30. |
![]() |
>128 | 8 | II |
31. |
![]() |
>128 | 4 | II |
32. |
![]() |
128 | 8 | II |
35. |
![]() |
>128 | 8 | I |
14. |
![]() |
>128 | 64 | ** |
33. |
![]() |
>128 | 0.5 | I |
Control compounds | ||||
23. |
![]() |
>128 | >128 | ** |
25. |
![]() |
>128 | >128 | ** |
Known compounds