CHEBI:61521 - γ-glutamyl-γ-aminobutyraldehyde

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ChEBI Name γ-glutamyl-γ-aminobutyraldehyde
ChEBI ID CHEBI:61521
ChEBI ASCII Name gamma-glutamyl-gamma-aminobutyraldehyde
Definition An L-glutamine derivative that is L-glutamine in which a hydrogen attached to the amide nitrogen is replaced by a 4-oxobutyl group.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C9H16N2O4
Net Charge 0
Average Mass 216.23430
Monoisotopic Mass 216.111
InChI InChI=1S/C9H16N2O4/c10-7(9(14)15)3-4-8(13)11-5-1-2-6-12/h6-7H,1-5,10H2,(H,11,13)(H,14,15)/t7-/m0/s1
InChIKey JZNLEPLZUABCSQ-ZETCQYMHSA-N
SMILES [H]C(=O)CCCNC(=O)CC[C@H](N)C(O)=O
Metabolite of Species Details
Escherichia coli (NCBI:txid562) See: PubMed
Roles Classification
Chemical Role(s): Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
Biological Role(s): Escherichia coli metabolite
Any bacterial metabolite produced during a metabolic reaction in Escherichia coli.
mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
(via L-alpha-amino acid )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing γ-glutamyl-γ-aminobutyraldehyde (CHEBI:61521) has role Escherichia coli metabolite (CHEBI:76971)
γ-glutamyl-γ-aminobutyraldehyde (CHEBI:61521) is a L-glutamine derivative (CHEBI:24317)
γ-glutamyl-γ-aminobutyraldehyde (CHEBI:61521) is a aldehyde (CHEBI:17478)
γ-glutamyl-γ-aminobutyraldehyde (CHEBI:61521) is a non-proteinogenic L-α-amino acid (CHEBI:83822)
γ-glutamyl-γ-aminobutyraldehyde (CHEBI:61521) is tautomer of γ-glutamyl-γ-aminobutyraldehyde zwitterion (CHEBI:61508)
Incoming γ-glutamyl-γ-aminobutyraldehyde zwitterion (CHEBI:61508) is tautomer of γ-glutamyl-γ-aminobutyraldehyde (CHEBI:61521)
IUPAC Name
N-(4-oxobutyl)-L-glutamine
Synonym Source
γ-glutamyl-γ-aminobutanal ChEBI
Manual Xref Database
C15700 KEGG COMPOUND
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Last Modified
25 January 2016