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 No supplier information found for this compound. 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