GREP C05332

Selected compound(s)

C05332 2-Phenylethylamine

Each orphan metabolite is emphasized in bold. Click [Fig] on the left hand, and the image of the reaction is shown.
[Suggested reactions | Reported reactions]

Suggested reactions

[Fig] 1.4.1.- : 2-Phenylethylamine + H2O + NAD+ = Phenylacetaldehyde + NADH + Ammonia
[Fig] 1.4.1.- : 2-Phenylethylamine + H2O + NAD+ = Phenylacetaldehyde + NADH + H+ + Ammonia
[Fig] 1.4.1.- : 2-Phenylethylamine + H2O + NADP+ = Phenylacetaldehyde + NADPH + Ammonia
[Fig] 1.4.1.- : 2-Phenylethylamine + H2O + NADP+ = Phenylacetaldehyde + NADPH + H+ + Ammonia
[Fig] 1.4.1.- : 2-Phenylethylamine + NAD+ + H2O = Phenylacetaldehyde + Ammonia + NADH
[Fig] 1.4.1.- : 2-Phenylethylamine + NAD+ + H2O = Phenylacetaldehyde + Ammonia + NADH + H+
[Fig] 1.4.1.- : 2-Phenylethylamine + NADP+ + H2O = Phenylacetaldehyde + Ammonia + NADPH
[Fig] 1.4.1.- : 2-Phenylethylamine + NADP+ + H2O = Phenylacetaldehyde + Ammonia + NADPH + H+
[Fig] 1.4.3.- : 2-Phenylethylamine + H2O + O2 = Phenylacetaldehyde + Ammonia + H2O2
[Fig] 1.14.11.- : 2-Phenylethylamine + O2 + 2-Ketoglutaric acid = 2-Phenylacetamide + CO2 + Butanedionic acid
[Fig] 1.14.13.- : 2-Phenylacetamide + H2O + NAD+ = 2-Phenylethylamine + NADH + O2 + H+
[Fig] 1.14.13.- : 2-Phenylacetamide + H2O + NADP+ = 2-Phenylethylamine + NADPH + O2 + H+
[Fig] 1.14.16.- : 2-Phenylacetamide + 6,7-Dihydrobiopterin + H2O = 2-Phenylethylamine + 2-Amino-6-(1,2-dihydroxypropyl)-5,6,7,8-tetrahydoro-4(1H)- pteridinone + O2
[Fig] 1.14.17.- : 2-Phenylethylamine + Vitamin C + O2 = 2-Phenylacetamide + Dehydroascorbate + H2O
[Fig] 1.17.1.- : 2-Phenylethylamine + H2O + NADP+ = 2-Phenylacetamide + NADPH + H+
[Fig] 1.17.3.- : 2-Phenylethylamine + H2O + O2 = 2-Phenylacetamide + H2O2
[Fig] 2.1.1.- : 2-Phenylethylamine + S-Adenosyl-L-methionine = Amphetamine + S-Adenosyl-L-homocysteine
[Fig] 2.1.1.- : 2-Phenylethylamine + S-Adenosyl-L-methionine = Amphetamine + S-Adenosyl-L-homocysteine + H+
[Fig] 2.1.1.- : 2-Phenylethylamine + S-Adenosyl-L-methionine = Dextroamphetamine + S-Adenosyl-L-homocysteine
[Fig] 2.1.1.- : 2-Phenylethylamine + S-Adenosyl-L-methionine = Dextroamphetamine + S-Adenosyl-L-homocysteine + H+
[Fig] 2.1.2.- : (S)-alpha-Amino-beta-phenylpropionic acid + THF = 2-Phenylethylamine + 10-Formyl-THF
[Fig] 2.3.1.- : 2-Phenylethylamine + Acetyl phosphate = N-(2-phenylethyl)-acetamide + Orthophosphate
[Fig] 2.3.1.- : N-(2-phenylethyl)-acetamide + CoA = 2-Phenylethylamine + Acetyl-CoA
[Fig] 2.6.1.- : Phenylacetaldehyde + L-Glutamate = 2-Phenylethylamine + 2-Ketoglutaric acid
[Fig] 2.6.1.- : 2-Phenylethylamine + Pyridoxal 5'-phosphate = Phenylacetaldehyde + Pyridoxamine 5'-phosphate
[Fig] 3.3.2.- : Amphetamine + H2O = 2-Phenylethylamine + Methanol
[Fig] 3.3.2.- : Dextroamphetamine + H2O = 2-Phenylethylamine + Methanol
[Fig] 3.5.1.- : N-(2-phenylethyl)-acetamide + H2O = 2-Phenylethylamine + Acetate
[Fig] 3.5.99.- : 2-Phenylethylamine + H2O = Phenethyl alcohol + Ammonia
[Fig] 3.7.1.- : (S)-alpha-Amino-beta-phenylpropionic acid + H2O = 2-Phenylethylamine + Formate
[Fig] 4.1.1.- : 2-Phenylethylamine + CO2 = (S)-alpha-Amino-beta-phenylpropionic acid
[Fig] 6.3.4.- : Phenethyl alcohol + ATP + Ammonia = 2-Phenylethylamine + ADP + Orthophosphate
[Fig] 6.3.4.- : Phenethyl alcohol + ATP + Ammonia = 2-Phenylethylamine + Diphosphate + 5'-AMP
[Fig] 6.4.1.- : (S)-alpha-Amino-beta-phenylpropionic acid + ADP + Orthophosphate = 2-Phenylethylamine + Formate + ATP
[Fig] 6.4.1.- : 2-Phenylethylamine + ATP + Acid carbonate = (S)-alpha-Amino-beta-phenylpropionic acid + ADP + Orthophosphate

Reported reactions

[Fig] EC 1.4.99.4 : 2-Phenylethylamine + H2O + Acceptor = Phenylacetaldehyde + Ammonia + Reduced acceptor
[Fig] EC 1.4.3.4 : 2-Phenylethylamine + O2 + H2O = Phenylacetaldehyde + Ammonia + H2O2
[Fig] EC 1.4.3.6 : 2-Phenylethylamine + O2 + H2O = Phenylacetaldehyde + Ammonia + H2O2
[Fig] EC 4.1.1.28 : (S)-alpha-Amino-beta-phenylpropionic acid = 2-Phenylethylamine + CO2
[Fig] EC 4.1.1.53 : (S)-alpha-Amino-beta-phenylpropionic acid = 2-Phenylethylamine + CO2

GREP v1.0.2 http://bisscat.org/GREP/
Developed by Masaaki Kotera (2008), Department of Biochemistry, Trinity College Dublin.
Science Foundation of Ireland is gratefully acknowledged.