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 Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Formula C5H9NO3 Net Charge 0 Average Mass 131.12990 Monoisotopic Mass 131.05824 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 View more database links Registry Numbers Types Sources 1704370 Beilstein Registry Number Beilstein 496-92-4 CAS Registry Number ChemIDplus Last Modified 20 November 2019