N-carbamoyl-beta-alanine (CHEBI:18261)

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ChEBI Name	N-carbamoyl-β-alanine

ChEBI ID	CHEBI:18261

ChEBI ASCII Name	N-carbamoyl-beta-alanine

Definition	A β-alanine derivative that is propionic acid bearing a ureido group at position 3.

Stars	This entity has been manually annotated by the ChEBI Team.

Secondary ChEBI IDs	CHEBI:21690, CHEBI:46352, CHEBI:12495, CHEBI:1671

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Formula

C4H8N2O3

Net Charge

Average Mass

132.11800

Monoisotopic Mass

132.05349

InChI

InChI=1S/C4H8N2O3/c5-4(9)6-2-1-3(7)8/h1-2H2,(H,7,8)(H3,5,6,9)

InChIKey

JSJWCHRYRHKBBW-UHFFFAOYSA-N

SMILES

NC(=O)NCCC(O)=O

Metabolite of Species	Details
Mus musculus (NCBI:txid10090)	Source: BioModels - MODEL1507180067 See: PubMed

Roles Classification
Biological Role(s):	metabolite Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites. mouse metabolite Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).

ChEBI Ontology
Outgoing	N-carbamoyl-β-alanine (CHEBI:18261) has functional parent propionic acid (CHEBI:30768) N-carbamoyl-β-alanine (CHEBI:18261) has role metabolite (CHEBI:25212) N-carbamoyl-β-alanine (CHEBI:18261) has role mouse metabolite (CHEBI:75771) N-carbamoyl-β-alanine (CHEBI:18261) is a β-alanine derivative (CHEBI:22823) N-carbamoyl-β-alanine (CHEBI:18261) is conjugate acid of N-carbamoyl-β-alaninate (CHEBI:11892)

Incoming	N-carbamoyl-β-alaninate (CHEBI:11892) is conjugate base of N-carbamoyl-β-alanine (CHEBI:18261)

IUPAC Names

3-(carbamoylamino)propanoic acid

N-carbamoyl-β-alanine

Synonyms	Sources
3-[(aminocarbonyl)amino]propanoic acid	ChEBI
3-Ureidopropanoate	KEGG COMPOUND
3-ureidopropanoic acid	HMDB
3-Ureidopropionate	KEGG COMPOUND
3-Ureidopropionic acid	HMDB
beta-Ureidopropionic acid	KEGG COMPOUND
N-(AMINOCARBONYL)-BETA-ALANINE	PDBeChem
N-(aminocarbonyl)-β-alanine	ChemIDplus
N-Carbamoyl-beta-alanine	KEGG COMPOUND
N-carbamoyl-beta-alanine	PDBeChem
N-carbamoyl-beta-alanine	ChEBI
Ureidopropanoic acid	ChEBI
Ureidopropionic acid	HMDB

Last Modified

27 January 2016