Selected compound(s)
- C01624 3,4-Dihydro-3,8-dihydroxy-1(2H)-naphthalenone
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.- : 3,4-Dihydro-3,8-dihydroxy-1(2H)-naphthalenone + NAD+ = 1,3,8-Naphthalenertriol + NADH + H+
- [Fig] 1.1.3.- : 3,4-Dihydro-3,8-dihydroxy-1(2H)-naphthalenone + O2 = 1,3,8-Naphthalenertriol + H2O2
- [Fig] 1.1.4.- : 1,3,8-Naphthalenertriol + 1,4-Dithiothreitol = 3,4-Dihydro-3,8-dihydroxy-1(2H)-naphthalenone + Oxidized dithiothreitol
- [Fig] 1.1.4.- : 1,3,8-Naphthalenertriol + Reduced thioredoxin = 3,4-Dihydro-3,8-dihydroxy-1(2H)-naphthalenone + Oxidized thioredoxin
- [Fig] 1.1.5.- : 1,3,8-Naphthalenertriol + CoQH2 = 3,4-Dihydro-3,8-dihydroxy-1(2H)-naphthalenone + CoQ
- [Fig] 1.1.99.- : 3,4-Dihydro-3,8-dihydroxy-1(2H)-naphthalenone + FAD = 1,3,8-Naphthalenertriol + FADH2
- [Fig] 1.1.99.- : 3,4-Dihydro-3,8-dihydroxy-1(2H)-naphthalenone + Coenzyme F420 = 1,3,8-Naphthalenertriol + Reduced coenzyme F420
Reported reactions
- [Fig] EC 1.1.1.252 : 3,4-Dihydro-3,8-dihydroxy-1(2H)-naphthalenone + NADP+ = 1,3,8-Naphthalenertriol + NADPH
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.