EC Number |
Reaction |
Reference |
---|
1.4.3.4 | RCH2NHR' + H2O + O2 = RCHO + R'NH2 + H2O2 |
catalysis occur via proton abstraction mechanisms |
688481 |
1.4.3.4 | RCH2NHR' + H2O + O2 = RCHO + R'NH2 + H2O2 |
mechanism |
394575, 394576 |
1.4.3.4 | RCH2NHR' + H2O + O2 = RCHO + R'NH2 + H2O2 |
mechanism of monoamine oxidase A |
394575 |
1.4.3.4 | RCH2NHR' + H2O + O2 = RCHO + R'NH2 + H2O2 |
mechanism of monoamine oxidase A and B |
394555 |
1.4.3.4 | RCH2NHR' + H2O + O2 = RCHO + R'NH2 + H2O2 |
ping-pong kinetic mechanism |
394559, 394561 |
1.4.3.4 | RCH2NHR' + H2O + O2 = RCHO + R'NH2 + H2O2 |
reaction mechanism of C-H bond cleavage, MAO B shows H tunneling to contribute in the H transfer step, overview |
711205 |
1.4.3.4 | RCH2NHR' + H2O + O2 = RCHO + R'NH2 + H2O2 |
reaction mechanism of C-H bond cleavage, overview |
711205 |
1.4.3.4 | RCH2NHR' + H2O + O2 = RCHO + R'NH2 + H2O2 |
reaction mechanism of C-H bond cleavage, overview. MAO oxidation of benzylamines and phenethylamines exhibit large deuterium kinetic isotope effects showing, in most instances, that C-H bond cleavage is rate limiting in catalysis |
711205 |