Selected compound(s)
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] 1.1.1.255 : Phloretin + NAD+ = 4',5,7-Trihydroxyflavanone + NADH + H+
- [Fig] 1.3.1.- : Phloretin + NAD+ = 2'4'6'4-Tetrahydroxychalcone + NADH + H+
- [Fig] 1.3.1.- : 2'4'6'4-Tetrahydroxychalcone + NADPH + H+ = Phloretin + NADP+
- [Fig] 1.3.3.- : Phloretin + O2 = 2'4'6'4-Tetrahydroxychalcone + H2O2
- [Fig] 1.3.4.- : 2'4'6'4-Tetrahydroxychalcone + 1,4-Dithiothreitol = Phloretin + Oxidized dithiothreitol
- [Fig] 1.3.5.- : 2'4'6'4-Tetrahydroxychalcone + CoQH2 = Phloretin + CoQ
- [Fig] 1.3.99.- : Phloretin + FAD = 2'4'6'4-Tetrahydroxychalcone + FADH2
- [Fig] 1.3.99.- : Phloretin + Coenzyme F420 = 2'4'6'4-Tetrahydroxychalcone + Reduced coenzyme F420
- [Fig] 1.14.13.- : Phloretin + H2O + NAD+ = 4,2',4'-Trihydroxydihydrochalcone + NADH + O2 + H+
- [Fig] 1.14.13.- : Phloretin + H2O + NADP+ = 4,2',4'-Trihydroxydihydrochalcone + NADPH + O2 + H+
- [Fig] 2.1.1.- : Phloretin + S-Adenosyl-L-methionine = Asebogenin + S-Adenosyl-L-homocysteine
- [Fig] 2.1.1.- : Phloretin + S-Adenosyl-L-methionine = Asebogenin + S-Adenosyl-L-homocysteine + H+
- [Fig] 2.4.1.- : Orthophosphate + Phlorhizin = D-Glucose 1-phosphate + Phloretin
- [Fig] 3.2.1.- : Phlorhizin + H2O = D-Glucose + Phloretin
- [Fig] 3.2.1.- : Phlorhizin + H2O = beta-D-Glucose + Phloretin
- [Fig] 3.2.1.- : Glycyphyllin + H2O = 6-Deoxy-L-mannose + Phloretin
- [Fig] 3.3.2.- : Asebogenin + H2O = Phloretin + Methanol
- [Fig] 3.7.1.- : Phloretin + H2O = 1,3,5-Benzenetriol + 3-(4-Hydroxyphenyl)propionic acid
- [Fig] 4.2.2.- : Phlorhizin = Phloretin + Lichenan
- [Fig] 6.4.1.- : 1,3,5-Benzenetriol + 3-(4-Hydroxyphenyl)propionic acid + ATP = Phloretin + ADP + Orthophosphate
- [Fig] 6.4.1.- : 1,3,5-Benzenetriol + 3-(4-Hydroxyphenyl)propionic acid + ATP = Phloretin + Diphosphate + 5'-AMP
Reported reactions
- [Fig] EC 3.7.1.4 : Phloretin + H2O = 3-(4-Hydroxyphenyl)propionic acid + 1,3,5-Benzenetriol
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.