CHEBI:32814 - N-carbamoyl-L-aspartate(2−)

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ChEBI Name N-carbamoyl-L-aspartate(2−) ChEBI ID CHEBI:32814 ChEBI ASCII Name N-carbamoyl-L-aspartate(2-) Definition An N-carbamoyl-L-α-amino acid anion obtained by deprotonation of the carboxy groups of N-carbamoyl-L-aspartic acid. Stars This entity has been manually annotated by the ChEBI Team. Secondary ChEBI IDs CHEBI:12593, CHEBI:21687 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 C5H6N2O5 Net Charge -2 Average Mass 174.11150 Monoisotopic Mass 174.02877 InChI InChI=1S/C5H8N2O5/c6-5(12)7-2(4(10)11)1-3(8)9/h2H,1H2,(H,8,9)(H,10,11)(H3,6,7,12)/p-2/t2-/m0/s1 InChIKey HLKXYZVTANABHZ-REOHCLBHSA-L SMILES NC(=O)N[C@@H](CC([O-])=O)C([O-])=O Metabolite of Species Details Saccharomyces cerevisiae (NCBI:txid4932) Source: yeast.sf.net See: PubMed Homo sapiens (NCBI:txid9606) See: DOI Roles Classification Biological Role(s): 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). View more via ChEBI Ontology ChEBI Ontology Outgoing N-carbamoyl-L-aspartate(2−) (CHEBI:32814) has role Saccharomyces cerevisiae metabolite (CHEBI:75772) N-carbamoyl-L-aspartate(2−) (CHEBI:32814) has role human metabolite (CHEBI:77746) N-carbamoyl-L-aspartate(2−) (CHEBI:32814) is a N-carbamoyl-L-α-amino acid anion (CHEBI:58865) N-carbamoyl-L-aspartate(2−) (CHEBI:32814) is conjugate base of N-carbamoyl-L-aspartic acid (CHEBI:15859) Incoming N-carbamoyl-L-aspartic acid (CHEBI:15859) is conjugate acid of N-carbamoyl-L-aspartate(2−) (CHEBI:32814) IUPAC Name N-carbamoyl-L-aspartate Synonyms Sources L-ureidosuccinate HMDB N-carbamoyl-L-aspartate ChEBI N-carbamoyl-L-aspartate UniProt N-carbamoyl-L-aspartate dianion ChEBI Manual Xrefs Databases CARBAMYUL-L-ASPARTATE MetaCyc HMDB0000828 HMDB View more database links Registry Number Type Source 3671739 Reaxys Registry Number Reaxys Citation Type Source 21045288 PubMed citation Europe PMC Last Modified 13 November 2017