EC Number   |
Substrates |
Products |
Reversibility |
|---|
    3.5.5.7 | (E)-2-methyl-2-butenenitrile + H2O |
regioselective hydrolysis, no detectable conversion of (Z)-2-methyl-2-butenenitrile |
(E)-2-methyl-2-butenoic acid + NH3 |
- |
? |
| 3.5.5.7 | 1,4-dicyano-2-butene + H2O |
42.6% of the activity with crotononitrile |
? |
- |
? |
| 3.5.5.7 | 1,4-dicyanobutane + H2O |
114.3% activity compared to 3-cyanopyridine |
? |
- |
? |
| 3.5.5.7 | 1,8-dicyanooctane + H2O |
114.3% activity compared to 3-cyanopyridine |
? |
- |
? |
| 3.5.5.7 | 1-cyclohexeneacetonitrile + H2O |
18.2% of the activity with crotononitrile |
1-cyclohexene carboxylate + NH3 |
- |
? |
| 3.5.5.7 | 1-cyclopenteneacetonitrile + H2O |
24.9% of the activity with crotononitrile |
1-cyclopentene carboxylate + NH3 |
- |
? |
| 3.5.5.7 | 2 fumarodinitrile + 3 H2O |
11% compared to the activity with 3-hexenedinitrile. Fumarodinitrile is converted to the monocarboxylate and the monocarboxamide in a ratio of about 65:35 |
3-cyanoacrylamide + 3-cyanoacrylic acid + NH3 |
- |
? |
| 3.5.5.7 | 2,4-dicyano-1-butene + H2O |
127% of the activity with crotononitrile |
? |
- |
? |
| 3.5.5.7 | 2,6-dichlorobenzonitrile + H2O |
- |
2,6-dichlorobenzamide + ? |
- |
? |
| 3.5.5.7 | 2-aminocrotononitrile + H2O |
30.3% of the activity with crotononitrile |
2-aminocrotonic acid + NH3 |
- |
? |
