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> Main
CHEBI:28297 - hydantoin-5-propionic acid
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ChEBI Ontology
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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
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Formula
C6H8N2O4
Net Charge
0
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 (Br
o
nsted 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.
View more via ChEBI Ontology
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
Manual Xrefs
Databases
C05565
KEGG COMPOUND
HMDB0001212
HMDB
View more database links
Registry Numbers
Types
Sources
5624-26-0
CAS Registry Number
ChemIDplus
83925
Reaxys Registry Number
Reaxys
Citations
Types
Sources
13960896
PubMed citation
Europe PMC
3760095
PubMed citation
Europe PMC
5835442
PubMed citation
Europe PMC
Last Modified
29 September 2016