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> Main
CHEBI:1670 - 3-ureidoisobutyric acid
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ChEBI Name
3-ureidoisobutyric acid
ChEBI ID
CHEBI:1670
Definition
A ureidocarboxylic acid that is 2-methylpropanoic acid substituted by a carbamoylamino group at position 3.
Stars
This entity has been manually annotated by the ChEBI Team.
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Formula
C5H10N2O3
Net Charge
0
Average Mass
146.14458
Monoisotopic Mass
146.06914
InChI
InChI=1S/C5H10N2O3/c1-3(4(8)9)2-7-5(6)10/h3H,2H2,1H3,(H,8,9)(H3,6,7,10)
InChIKey
PHENTZNALBMCQD-UHFFFAOYSA-N
SMILES
CC(CNC(N)=O)C(O)=O
Metabolite of Species
Details
Mus musculus
(NCBI:txid10090)
Source: BioModels - MODEL1507180067 See:
PubMed
Homo sapiens
(NCBI:txid9606)
See:
DOI
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):
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (
Homo sapiens
).
mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (
Mus musculus
).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
3-ureidoisobutyric acid (
CHEBI:1670
)
has role
human metabolite (
CHEBI:77746
)
3-ureidoisobutyric acid (
CHEBI:1670
)
has role
mouse metabolite (
CHEBI:75771
)
3-ureidoisobutyric acid (
CHEBI:1670
)
is a
ureidocarboxylic acid (
CHEBI:49052
)
3-ureidoisobutyric acid (
CHEBI:1670
)
is conjugate acid of
3-ureidoisobutyrate(1−) (
CHEBI:74414
)
Incoming
3-ureidoisobutyrate(1−) (
CHEBI:74414
)
is conjugate base of
3-ureidoisobutyric acid (
CHEBI:1670
)
IUPAC Name
3-carbamoylamino-2-methylpropanoic acid
Synonyms
Sources
3-((aminocarbonyl)amino)-2-methylpropanoic acid
ChemIDplus
3-Ureidoisobutyrate
KEGG COMPOUND
β-UBA
ChemIDplus
β-ureidoisobutyric acid
ChemIDplus
Manual Xrefs
Databases
3-UREIDO-ISOBUTYRATE
MetaCyc
C05100
KEGG COMPOUND
HMDB0002031
HMDB
View more database links
Registry Numbers
Types
Sources
1768736
Reaxys Registry Number
Reaxys
2905-86-4
CAS Registry Number
ChemIDplus
Citation
Type
Source
11675655
PubMed citation
Europe PMC
Last Modified
27 January 2016