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Results 1 - 8 of 8
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EC Number Reaction Commentary Reference
Show all pathways known for 1.4.3.4Display the word mapDisplay the reaction diagram Show all sequences 1.4.3.4RCH2NHR' + H2O + O2 = RCHO + R'NH2 + H2O2 catalysis occur via proton abstraction mechanisms 688481
Show all pathways known for 1.4.3.4Display the word mapDisplay the reaction diagram Show all sequences 1.4.3.4RCH2NHR' + H2O + O2 = RCHO + R'NH2 + H2O2 mechanism 394575, 394576
Show all pathways known for 1.4.3.4Display the word mapDisplay the reaction diagram Show all sequences 1.4.3.4RCH2NHR' + H2O + O2 = RCHO + R'NH2 + H2O2 mechanism of monoamine oxidase A 394575
Show all pathways known for 1.4.3.4Display the word mapDisplay the reaction diagram Show all sequences 1.4.3.4RCH2NHR' + H2O + O2 = RCHO + R'NH2 + H2O2 mechanism of monoamine oxidase A and B 394555
Show all pathways known for 1.4.3.4Display the word mapDisplay the reaction diagram Show all sequences 1.4.3.4RCH2NHR' + H2O + O2 = RCHO + R'NH2 + H2O2 ping-pong kinetic mechanism 394559, 394561
Show all pathways known for 1.4.3.4Display the word mapDisplay the reaction diagram Show all sequences 1.4.3.4RCH2NHR' + 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
Show all pathways known for 1.4.3.4Display the word mapDisplay the reaction diagram Show all sequences 1.4.3.4RCH2NHR' + H2O + O2 = RCHO + R'NH2 + H2O2 reaction mechanism of C-H bond cleavage, overview 711205
Show all pathways known for 1.4.3.4Display the word mapDisplay the reaction diagram Show all sequences 1.4.3.4RCH2NHR' + 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
Results 1 - 8 of 8
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