CHEBI:17232 - L-glutamic 5-semialdehyde

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ChEBI Name L-glutamic 5-semialdehyde
ChEBI ID CHEBI:17232
ChEBI ASCII Name L-glutamic 5-semialdehyde
Definition A glutamic semialdehyde arising from formal reduction of the side-chain carboxy group of L-glutamic acid.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:6225, CHEBI:13109, CHEBI:21302
Supplier Information
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Formula C5H9NO3
Net Charge 0
Average Mass 131.12990
Monoisotopic Mass 131.058
InChI InChI=1S/C5H9NO3/c6-4(5(8)9)2-1-3-7/h3-4H,1-2,6H2,(H,8,9)/t4-/m0/s1
InChIKey KABXUUFDPUOJMW-BYPYZUCNSA-N
SMILES [H]C(=O)CC[C@H](N)C(O)=O
Metabolite of Species Details
Mus musculus (NCBI:txid10090) Source: BioModels - MODEL1507180067 See: PubMed
Saccharomyces cerevisiae (NCBI:txid4932) Source: yeast.sf.net See: PubMed
Escherichia coli (NCBI:txid562) See: PubMed
Homo sapiens (NCBI:txid9606) See: DOI
Roles Classification
Chemical Role(s): 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.
Saccharomyces cerevisiae metabolite
Any fungal metabolite produced during a metabolic reaction in Baker's yeast (Saccharomyces cerevisiae ).
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing L-glutamic 5-semialdehyde (CHEBI:17232) has role Escherichia coli metabolite (CHEBI:76971)
L-glutamic 5-semialdehyde (CHEBI:17232) has role Saccharomyces cerevisiae metabolite (CHEBI:75772)
L-glutamic 5-semialdehyde (CHEBI:17232) has role human metabolite (CHEBI:77746)
L-glutamic 5-semialdehyde (CHEBI:17232) has role mouse metabolite (CHEBI:75771)
L-glutamic 5-semialdehyde (CHEBI:17232) is a glutamic semialdehyde (CHEBI:24313)
L-glutamic 5-semialdehyde (CHEBI:17232) is tautomer of L-glutamic 5-semialdehyde zwitterion (CHEBI:58066)
Incoming 2-acetamido-5-oxopentanoic acid (CHEBI:16319) has functional parent L-glutamic 5-semialdehyde (CHEBI:17232)
N-succinyl-L-glutamic 5-semialdehyde (CHEBI:27657) has functional parent L-glutamic 5-semialdehyde (CHEBI:17232)
L-4-hydroxyglutamic semialdehyde (CHEBI:27809) has functional parent L-glutamic 5-semialdehyde (CHEBI:17232)
L-glutamic 5-semialdehyde residue (CHEBI:41433) is substituent group from L-glutamic 5-semialdehyde (CHEBI:17232)
L-glutamic 5-semialdehyde zwitterion (CHEBI:58066) is tautomer of L-glutamic 5-semialdehyde (CHEBI:17232)
IUPAC Name
(2S)-2-amino-5-oxopentanoic acid
Synonyms Sources
5-oxo-L-norvaline ChEBI
L-Glutamate 5-semialdehyde KEGG COMPOUND
L-Glutamate gamma-semialdehyde KEGG COMPOUND
Manual Xrefs Databases
C00007475 KNApSAcK
C01165 KEGG COMPOUND
ILG PDBeChem
View more database links
Registry Numbers Types Sources
1704370 Beilstein Registry Number Beilstein
496-92-4 CAS Registry Number ChemIDplus
Last Modified
27 January 2016