EC Number   |
Inhibitors |
Structure |
|---|
    3.2.1.1 | (2H)-1,4-benzoxazin-3(4H)-one |
- |
   |
| 3.2.1.1 | (NH4)2SO4 |
- |
|
| 3.2.1.1 | (NH4)2SO4 |
slight inhibition at 5-10 mM |
|
| 3.2.1.1 | 1,10-phenanthroline |
1 mM, 39% loss of activity of the membrane-bound enzyme |
|
| 3.2.1.1 | 1,10-phenanthroline |
10.7% inhibition at 10 mM |
|
| 3.2.1.1 | 1,10-phenanthroline |
22% inhibition at 10 mM |
|
| 3.2.1.1 | 1,2,3,4,6-pentagalloyl-beta-D-glucose |
mixed non-competitive inhibition, KEI: 0.0026 mM, KEIS: 0.0039 mM, tested in a concentration range of 0.04 to 0.5 mM, reduced inhibitory efficiency of the mutants W58L and Y151M with 92 and 97% remaining enzyme activity at 0.00235 mM inhibitor concentration, respectively, pH 6.0, 37°C |
|
| 3.2.1.1 | 1-cyclohexyl-3-(morpholinyl-4-ethyl)-carbodiimide |
40 mM, 50% inhibition after 20 min, 100 mM, 44% inhibition after 10 min in the presence of 1% starch |
|
| 3.2.1.1 | 2,4-dihydroxy-7-methoxy-(2H)-1,4-benzoxazin-3(4H)-one |
- |
|
| 3.2.1.1 | 2,4-Dinitro-1-fluorobenzene |
6 mM |
|
