1.14.17.1	1-(4-hydroxybenzyl)imidazole + ascorbate + O2	-	Bos taurus	4-hydroxybenzaldehyde + dehydroascorbate + H2O + ?	-	?	288094	
1.14.17.1	1-(4-hydroxybenzyl)imidazole + ascorbate + O2	-	Bos taurus	?	-	?	288096	
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 + ?	-	?	288091	
1.14.17.1	1-phenylethylamine + ascorbate + O2	-	Bos taurus	?	-	?	453851	
1.14.17.1	2-(4-hydroxyphenyl)prop-2-enylamine + ascorbate + O2	-	Bos taurus	?	-	?	288095	
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	-	?	363762	
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	-	?	288106	
1.14.17.1	2-chlorophenethylamine + ascorbate + O2	-	Bos taurus	2-amino-1-chloro-1-phenylethanol + dehydroascorbate + H2O	-	?	288107	
1.14.17.1	2-hydroxyphenethylamine + ascorbate + O2	-	Bos taurus	2-amino-1-phenylethane-1,1-diol + dehydroascorbate + H2O	-	?	288108	
1.14.17.1	2-phenylethylamine + ascorbate + O2	-	Bos taurus	?	-	?	288092