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] 1.14.11.- : Apigeninidin + O2 + 2-Ketoglutaric acid = 4',5,7-Trihydroxyflavone + CO2 + Butanedionic acid
- [Fig] 1.14.11.- : Apigeninidin + O2 + 2-Ketoglutaric acid = 4',5,7-Trihydroxyflavone + CO2 + Butanedionic acid + H+
- [Fig] 1.14.13.- : 4',5,7-Trihydroxyflavone + H2O + NAD+ = Apigeninidin + NADH + O2
- [Fig] 1.14.13.- : 4',5,7-Trihydroxyflavone + H2O + NAD+ = Apigeninidin + NADH + O2 + H+
- [Fig] 1.14.13.- : 4',5,7-Trihydroxyflavone + H2O + NADP+ = Apigeninidin + NADPH + O2
- [Fig] 1.14.13.- : 4',5,7-Trihydroxyflavone + H2O + NADP+ = Apigeninidin + NADPH + O2 + H+
- [Fig] 1.14.13.- : 1-Benzopyrylium, 3,5,7-trihydroxy-2-(4-hydroxyphenyl)-, chloride + H2O + NAD+ = Apigeninidin + NADH + O2 + H+
- [Fig] 1.14.13.- : 1-Benzopyrylium, 3,5,7-trihydroxy-2-(4-hydroxyphenyl)-, chloride + H2O + NADP+ = Apigeninidin + NADPH + O2 + H+
- [Fig] 1.14.13.- : Luteolinidin + H2O + NAD+ = Apigeninidin + NADH + O2 + H+
- [Fig] 1.14.13.- : Luteolinidin + H2O + NADP+ = Apigeninidin + NADPH + O2 + H+
- [Fig] 1.14.16.- : 4',5,7-Trihydroxyflavone + 6,7-Dihydrobiopterin + H2O = Apigeninidin + 2-Amino-6-(1,2-dihydroxypropyl)-5,6,7,8-tetrahydoro-4(1H)- pteridinone + O2
- [Fig] 1.14.17.- : Apigeninidin + Vitamin C + O2 = 4',5,7-Trihydroxyflavone + Dehydroascorbate + H2O
- [Fig] 1.17.1.- : Apigeninidin + H2O + NAD+ = 4',5,7-Trihydroxyflavone + NADH + H+
- [Fig] 1.17.1.- : Apigeninidin + H2O + NADP+ = 4',5,7-Trihydroxyflavone + NADPH + H+
- [Fig] 1.17.3.- : Apigeninidin + H2O + O2 = 4',5,7-Trihydroxyflavone + H2O2
- [Fig] 1.17.4.- : Apigeninidin + H2O + Oxidized thioredoxin = 4',5,7-Trihydroxyflavone + Reduced thioredoxin
- [Fig] 1.17.4.- : Apigeninidin + H2O + Oxidized dithiothreitol = 4',5,7-Trihydroxyflavone + 1,4-Dithiothreitol
- [Fig] 4.2.1.- : Apigeninidin + H2O = 4',5,7-Trihydroxyflavanone
Reported reactions
- No reported reactions found.
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.