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InChI=1S/CH4O/c1-2/h2H,1H3
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ChEBI
> Main
CHEBI:50616 - iminoaspartic acid
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ChEBI Name
iminoaspartic acid
ChEBI ID
CHEBI:50616
Definition
A succinic acid derivative having an imino group at the 2-position.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:5878, CHEBI:24784
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Formula
C4H5NO4
Net Charge
0
Average Mass
131.08684
Monoisotopic Mass
131.02186
InChI
InChI=1S/C4H5NO4/c5-2(4(8)9)1-3(6)7/h5H,1H2,(H,6,7)(H,8,9)
InChIKey
NMUOATVLLQEYHI-UHFFFAOYSA-N
SMILES
OC(=O)CC(=N)C(O)=O
Metabolite of Species
Details
Escherichia coli
(NCBI:txid562)
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):
Escherichia coli metabolite
Any bacterial metabolite produced during a metabolic reaction in
Escherichia coli
.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
iminoaspartic acid (
CHEBI:50616
)
has functional parent
succinic acid (
CHEBI:15741
)
iminoaspartic acid (
CHEBI:50616
)
has role
Escherichia coli
metabolite (
CHEBI:76971
)
iminoaspartic acid (
CHEBI:50616
)
is a
aspartic acid derivative (
CHEBI:22661
)
iminoaspartic acid (
CHEBI:50616
)
is a
C4-dicarboxylic acid (
CHEBI:66873
)
iminoaspartic acid (
CHEBI:50616
)
is a
ketimine (
CHEBI:33272
)
iminoaspartic acid (
CHEBI:50616
)
is conjugate acid of
iminoaspartate (
CHEBI:58831
)
iminoaspartic acid (
CHEBI:50616
)
is conjugate acid of
iminoaspartate(1−) (
CHEBI:77875
)
Incoming
iminoaspartate (
CHEBI:58831
)
is conjugate base of
iminoaspartic acid (
CHEBI:50616
)
iminoaspartate(1−) (
CHEBI:77875
)
is conjugate base of
iminoaspartic acid (
CHEBI:50616
)
IUPAC Name
2-iminobutanedioic acid
Synonyms
Sources
Iminoaspartate
KEGG COMPOUND
Iminoaspartic acid
KEGG COMPOUND
iminosuccinate
ChEBI
Iminosuccinate
KEGG COMPOUND
iminosuccinic acid
ChEBI
Manual Xrefs
Databases
C00007565
KNApSAcK
C05840
KEGG COMPOUND
View more database links
Registry Number
Type
Source
79067-61-1
CAS Registry Number
ChemIDplus
Last Modified
25 January 2016