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π§ͺ 4-Methylaminobutyrate
Appears in:
1 pathway
Produces:
5 compounds
Produced by:
1 transformation
Chemical Structure
π Properties
SMILES:
O=C([O-])CCCNC
InChI:
InChI=1S/C5H11NO2/c1-6-4-2-3-5(7)8/h6H,2-4H2,1H3,(H,7,8)/p-1
Database ID:
590
External:
View on PubChem β
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π¬ Reactant
4-Methylaminobutyrate
β
Methylamine
4-methylaminobutanoate oxidase (methylamine-forming)
(Eawag BBD reaction r1828)
(EC 1.5.3.21)
In pathway:
Nicotine
4-Methylaminobutyrate
β
Succinic semialdehyde
4-methylaminobutanoate oxidase (methylamine-forming)
(Eawag BBD reaction r1828)
(EC 1.5.3.21)
In pathway:
Nicotine
4-Methylaminobutyrate
β
4-aminobutanoate
4-methylaminobutanoate oxidase
(Eawag BBD reaction r1827)
(EC 1.5.3.19)
In pathway:
Nicotine
4-Methylaminobutyrate
β
Formaldehyde
4-methylaminobutanoate oxidase
(Eawag BBD reaction r1827)
(EC 1.5.3.19)
In pathway:
Nicotine
4-Methylaminobutyrate
β
Carbon Dioxide
Eawag BBD reaction r0503
In pathway:
Nicotine
π¬ Product
2,6-Dihydroxypseudooxynicotine
β
4-Methylaminobutyrate
2,6-dihydroxypseudooxynicotine hydrolase
(Eawag BBD reaction r0482)
(EC 3.7.1.9)
In pathway:
Nicotine
πΊοΈ All Pathways Containing This Compound
Nicotine
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