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] 1.14.13.- : Petunidin + H2O + NAD+ = 3,5,7-Trihydroxy-2-(4-hydroxy-3-methoxyphenyl)-1-benzopyrylium chloride + NADH + O2 + H+
- [Fig] 1.14.13.- : Petunidin + H2O + NADP+ = 3,5,7-Trihydroxy-2-(4-hydroxy-3-methoxyphenyl)-1-benzopyrylium chloride + NADPH + O2 + H+
- [Fig] 2.1.1.- : 1-Benzopyrylium, 3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)-, chloride + S-Adenosyl-L-methionine = Petunidin + S-Adenosyl-L-homocysteine
- [Fig] 2.1.1.- : 1-Benzopyrylium, 3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)-, chloride + S-Adenosyl-L-methionine = Petunidin + S-Adenosyl-L-homocysteine + H+
- [Fig] 2.1.1.- : Petunidin + S-Adenosyl-L-methionine = Malvidin + S-Adenosyl-L-homocysteine
- [Fig] 2.1.1.- : Petunidin + S-Adenosyl-L-methionine = Malvidin + S-Adenosyl-L-homocysteine + H+
- [Fig] 3.3.2.- : Malvidin + H2O = Petunidin + Methanol
- [Fig] 3.3.2.- : Petunidin + H2O = 1-Benzopyrylium, 3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)-, chloride + Methanol
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.