EC Number |
Substrates |
Organism |
Products |
Reversibility |
---|
1.14.17.1 | 1-(4-hydroxybenzyl)imidazole + ascorbate + O2 |
- |
Bos taurus |
4-hydroxybenzaldehyde + dehydroascorbate + H2O + ? |
- |
? |
1.14.17.1 | 1-(4-hydroxybenzyl)imidazole + ascorbate + O2 |
- |
Bos taurus |
? |
- |
? |
1.14.17.1 | 1-phenyl-1-aminomethylethene + ascorbate + O2 |
ascorbate and ferrocyanide can function as a electron donors |
Bos taurus |
2,3-dihydroxy-2-phenylpropylamine + dehydroascorbate + H2O + ? |
- |
? |
1.14.17.1 | 1-phenylethylamine + ascorbate + O2 |
- |
Bos taurus |
? |
- |
? |
1.14.17.1 | 2-(4-hydroxyphenyl)prop-2-enylamine + ascorbate + O2 |
- |
Bos taurus |
? |
- |
? |
1.14.17.1 | 2-aminoindane + ascorbate + O2 |
Stereochemistry is in contrast to the stereochemical course of pro-R hydroxylation of the DBH/phenethylamine reaction. Studies with stereospecifically deuterium labelled substrate show that the production of (1S)-aminoindanol ir the result of sterospecific pro-S hydrogen abstraction followed by the oxygen binding with overall retention of configuration |
Bos taurus |
trans-(1S,2S)-2-amino-1-indanol + H2O |
- |
? |
1.14.17.1 | 2-bromo-3-(p-hydroxyphenyl)-1-propene + ascorbate + O2 |
- |
Bos taurus |
2-bromo-3-hydroxy-3-(p-hydroxyphenyl)-1-propene + H2O |
- |
? |
1.14.17.1 | 2-chlorophenethylamine + ascorbate + O2 |
- |
Bos taurus |
2-amino-1-chloro-1-phenylethanol + dehydroascorbate + H2O |
- |
? |
1.14.17.1 | 2-hydroxyphenethylamine + ascorbate + O2 |
- |
Bos taurus |
2-amino-1-phenylethane-1,1-diol + dehydroascorbate + H2O |
- |
? |
1.14.17.1 | 2-phenylethylamine + ascorbate + O2 |
- |
Bos taurus |
? |
- |
? |