CHEBI:15859 - N-carbamoyl-L-aspartic acid

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ChEBI Name N-carbamoyl-L-aspartic acid
ChEBI ID CHEBI:15859
ChEBI ASCII Name N-carbamoyl-L-aspartic acid
Definition The L-enantiomer N-carbamoylaspartic acid.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:44316, CHEBI:12496, CHEBI:7257, CHEBI:21688
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Formula C5H8N2O5
Net Charge 0
Average Mass 176.12740
Monoisotopic Mass 176.04332
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)/t2-/m0/s1
InChIKey HLKXYZVTANABHZ-REOHCLBHSA-N
SMILES NC(=O)N[C@@H](CC(O)=O)C(O)=O
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): metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
Saccharomyces cerevisiae metabolite
Any fungal metabolite produced during a metabolic reaction in Baker's yeast (Saccharomyces cerevisiae ).
(via N-carbamoylaspartic acid )
Escherichia coli metabolite
Any bacterial metabolite produced during a metabolic reaction in Escherichia coli.
(via N-carbamoylaspartic acid )
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
(via N-carbamoylaspartic acid )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing N-carbamoyl-L-aspartic acid (CHEBI:15859) has role metabolite (CHEBI:25212)
N-carbamoyl-L-aspartic acid (CHEBI:15859) is a N-carbamoyl-L-amino acid (CHEBI:21686)
N-carbamoyl-L-aspartic acid (CHEBI:15859) is a N-carbamoylaspartic acid (CHEBI:64850)
N-carbamoyl-L-aspartic acid (CHEBI:15859) is a L-aspartic acid derivative (CHEBI:83978)
N-carbamoyl-L-aspartic acid (CHEBI:15859) is conjugate acid of N-carbamoyl-L-aspartate(2−) (CHEBI:32814)
Incoming N-carbamoyl-L-aspartate(2−) (CHEBI:32814) is conjugate base of N-carbamoyl-L-aspartic acid (CHEBI:15859)
IUPAC Name
N-carbamoyl-L-aspartic acid
Synonyms Sources
carbamyl-L-aspartic acid ChemIDplus
Carbamyl-L-aspartic acid HMDB
L-ureidosuccinic acid ChemIDplus
N-(aminocarbonyl)-L-aspartic acid ChemIDplus
N-Carbamoyl-L-aspartate KEGG COMPOUND
N-CARBAMOYL-L-ASPARTATE PDBeChem
N-carbamoyl-S-aspartic acid HMDB
Manual Xrefs Databases
C00007265 KNApSAcK
C00438 KEGG COMPOUND
Carbamoyl_aspartic_acid Wikipedia
DB04252 DrugBank
HMDB0000828 HMDB
NCD PDBeChem
View more database links
Registry Numbers Types Sources
13184-27-5 CAS Registry Number ChemIDplus
1726860 Beilstein Registry Number Beilstein
1726860 Reaxys Registry Number Reaxys
Citation Waiting for Citations Type Source
17439666 PubMed citation Europe PMC
Last Modified
23 October 2015