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π§ͺ 3-Methyl-5-hydroxy-6-(3-carboxy-3-oxopropenyl)-1H-2-pyridon
Appears in:
1 pathway
Produces:
2 compounds
Produced by:
1 transformation
Chemical Structure
π Properties
SMILES:
O=C([O-])C(=O)C=CC=1NC(=O)C(=CC1O)C
InChI:
InChI=1S/C10H9NO5/c1-5-4-8(13)6(11-9(5)14)2-3-7(12)10(15)16/h2-4,13H,1H3,(H,11,14)(H,15,16)/p-1/b3-2+
Database ID:
480
External:
View on PubChem β
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π¬ Reactant
3-Methyl-5-hydroxy-6-(3-carboxy-3-oxopropenyl)-1H-2-pyridon
β
2,5,6-Trihydroxy-3-methylpyridine
3-methyl-5-hydroxy-6-(3-carboxy-3-oxopropenyl)-1H-2-pyridon hydratase-adolase
(Eawag BBD reaction r0051)
(EC 4.2.1.-)
In pathway:
3-Methylquinoline
3-Methyl-5-hydroxy-6-(3-carboxy-3-oxopropenyl)-1H-2-pyridon
β
2-Oxobut-3-enanoate
3-methyl-5-hydroxy-6-(3-carboxy-3-oxopropenyl)-1H-2-pyridon hydratase-adolase
(Eawag BBD reaction r0051)
(EC 4.2.1.-)
In pathway:
3-Methylquinoline
π¬ Product
5,6-Dihydroxy-3-methyl-2-oxo-1,2-dihydroquinoline
β
3-Methyl-5-hydroxy-6-(3-carboxy-3-oxopropenyl)-1H-2-pyridon
5,6-dihydroxy-3-methyl-2-oxo-1,2-dihydroquinoline dioxygenase
(Eawag BBD reaction r0049)
(EC 1.13.11.-)
In pathway:
3-Methylquinoline
πΊοΈ All Pathways Containing This Compound
3-Methylquinoline
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