hydantoin-5-propionic acid (CHEBI:28297)

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ChEBI Name	hydantoin-5-propionic acid

ChEBI ID	CHEBI:28297

Definition	A imidazolidine-2,4-dione that is hydantoin substituted by a 2-carboxyethyl group at position 4.

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

Secondary ChEBI IDs	CHEBI:5774, CHEBI:24626, CHEBI:24627

Supplier Information

Download	Molfile XML SDF

Formula

C6H8N2O4

Net Charge

Average Mass

172.13870

Monoisotopic Mass

172.04841

InChI

InChI=1S/C6H8N2O4/c9-4(10)2-1-3-5(11)8-6(12)7-3/h3H,1-2H2,(H,9,10)(H2,7,8,11,12)

InChIKey

VWFWNXQAMGDPGG-UHFFFAOYSA-N

SMILES

OC(=O)CCC1NC(=O)NC1=O

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

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

ChEBI Ontology
Outgoing	hydantoin-5-propionic acid (CHEBI:28297) has functional parent hydantoin (CHEBI:27612) hydantoin-5-propionic acid (CHEBI:28297) has role metabolite (CHEBI:25212) hydantoin-5-propionic acid (CHEBI:28297) has role mouse metabolite (CHEBI:75771) hydantoin-5-propionic acid (CHEBI:28297) is a imidazolidine-2,4-dione (CHEBI:24628) hydantoin-5-propionic acid (CHEBI:28297) is a monocarboxylic acid (CHEBI:25384) hydantoin-5-propionic acid (CHEBI:28297) is conjugate acid of hydantoin-5-propionate (CHEBI:133476)

Incoming	hydantoin-5-propionate (CHEBI:133476) is conjugate base of hydantoin-5-propionic acid (CHEBI:28297)

IUPAC Name

3-(2,5-dioxoimidazolidin-4-yl)propanoic acid

Last Modified

29 September 2016