CHEBI:64850 - N-carbamoylaspartic acid

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ChEBI Name N-carbamoylaspartic acid
ChEBI ASCII Name N-carbamoylaspartic acid
Definition An N-carbamoylamino acid that is aspartic acid with one of its amino hydrogens replaced by a carbamoyl group.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C5H8N2O5
Net Charge 0
Average Mass 176.12740
Monoisotopic Mass 176.043
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)
Metabolite of Species Details
Mus musculus (NCBI:txid10090) See: MetaboLights Study
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): Saccharomyces cerevisiae metabolite
Any fungal metabolite produced during a metabolic reaction in Baker's yeast (Saccharomyces cerevisiae ).
Escherichia coli metabolite
Any bacterial metabolite produced during a metabolic reaction in Escherichia coli.
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
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ChEBI Ontology
Outgoing N-carbamoylaspartic acid (CHEBI:64850) has role Escherichia coli metabolite (CHEBI:76971)
N-carbamoylaspartic acid (CHEBI:64850) has role Saccharomyces cerevisiae metabolite (CHEBI:75772)
N-carbamoylaspartic acid (CHEBI:64850) has role human metabolite (CHEBI:77746)
N-carbamoylaspartic acid (CHEBI:64850) is a N-carbamoyl-amino acid (CHEBI:21689)
N-carbamoylaspartic acid (CHEBI:64850) is a aspartic acid derivative (CHEBI:22661)
N-carbamoylaspartic acid (CHEBI:64850) is a C4-dicarboxylic acid (CHEBI:66873)
N-carbamoylaspartic acid (CHEBI:64850) is conjugate acid of N-carbamoylaspartate(2-) (CHEBI:90158)
Incoming N-carbamoyl-D-aspartic acid (CHEBI:64852) is a N-carbamoylaspartic acid (CHEBI:64850)
N-carbamoyl-L-aspartic acid (CHEBI:15859) is a N-carbamoylaspartic acid (CHEBI:64850)
N-carbamoylaspartate(2-) (CHEBI:90158) is conjugate base of N-carbamoylaspartic acid (CHEBI:64850)
N-carbamoylaspartic acid
Synonyms Sources
2-Ureidobutanedioic acid HMDB
Carbamylaspartic acid HMDB
N-(Aminocarbonyl)-DL-aspartic acid ChemIDplus
Ureidosuccinic acid ChemIDplus
Manual Xref Database
Carbamoyl_aspartic_acid Wikipedia
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Registry Numbers Types Sources
1726859 Reaxys Registry Number Reaxys
923-37-5 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
131912 PubMed citation Europe PMC
13831 PubMed citation Europe PMC
13882306 PubMed citation Europe PMC
14367323 PubMed citation Europe PMC
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Last Modified
08 June 2016