Services
Research
Training
Industry
About us
ChEBI
Examples:
iron*
,
InChI=1S/CH4O/c1-2/h2H,1H3
,
caffeine
Advanced
Home
Advanced Search
Browse
Documentation
Download
Tools
About ChEBI
Submit
Contact us
DiNA
Statistics
Entity of the Month
Periodic Table
Ontology
Train online
User Manual
Annotation Manual
Developer Manual
FAQ's
BiNChE
libChEBI
Web Services
ChEBI
> Main
CHEBI:18237 - glutamic acid
Main
ChEBI Ontology
Automatic Xrefs
Reactions
Pathways
Models
ChEBI Name
glutamic acid
ChEBI ID
CHEBI:18237
Definition
An α-amino acid that is glutaric acid bearing a single amino substituent at position 2.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:24314, CHEBI:5431
Supplier Information
Download
Molfile
XML
SDF
Find compounds which contain this structure
Find compounds which resemble this structure
Take structure to the Advanced Search
Wikipedia
License
Read full article at Wikipedia
Formula
C5H9NO4
Net Charge
0
Average Mass
147.12930
Monoisotopic Mass
147.05316
InChI
InChI=1S/C5H9NO4/c6-3(5(9)10)1-2-4(7)8/h3H,1-2,6H2,(H,7,8)(H,9,10)
InChIKey
WHUUTDBJXJRKMK-UHFFFAOYSA-N
SMILES
NC(CCC(O)=O)C(O)=O
Metabolite of Species
Details
Mus musculus
(NCBI:txid10090)
Source: BioModels - MODEL1507180067 See:
PubMed
Daphnia magna
(NCBI:txid35525)
See: Mixtures of similarly acting compounds in Daphnia magna: From gene to metabolite and beyondTine Vandenbrouck, Oliver A.H. Jones, Nathalie Dom, Julian L. Griffin, Wim De CoenEnvironment International 36 (2010) 254-268
Roles Classification
Chemical Role
(s):
Bronsted base
A molecular entity capable of accepting a hydron from a donor (Br
o
nsted acid).
(via
organic amino compound
)
Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Br
o
nsted base).
(via
oxoacid
)
Biological Role
(s):
fundamental metabolite
Any metabolite produced by all living cells.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
glutamic acid (
CHEBI:18237
)
has part
2-carboxyethyl group (
CHEBI:50329
)
glutamic acid (
CHEBI:18237
)
has role
fundamental metabolite (
CHEBI:78675
)
glutamic acid (
CHEBI:18237
)
is a
α-amino acid (
CHEBI:33704
)
glutamic acid (
CHEBI:18237
)
is a
polar amino acid (
CHEBI:26167
)
glutamic acid (
CHEBI:18237
)
is conjugate acid of
glutamate(1−) (
CHEBI:14321
)
Incoming
γ-Glu-Leu (
CHEBI:68433
)
has functional parent
glutamic acid (
CHEBI:18237
)
γ-glutamyl-
Se
-methylselenocysteine (
CHEBI:28776
)
has functional parent
glutamic acid (
CHEBI:18237
)
γ-glutamylphenylalanine (
CHEBI:82966
)
has functional parent
glutamic acid (
CHEBI:18237
)
γ-glutamylthreonine (
CHEBI:82968
)
has functional parent
glutamic acid (
CHEBI:18237
)
γGluCys(IAN)Glu (
CHEBI:64978
)
has functional parent
glutamic acid (
CHEBI:18237
)
glutamic acid derivative (
CHEBI:24315
)
has functional parent
glutamic acid (
CHEBI:18237
)
D
-glutamic acid (
CHEBI:15966
)
is a
glutamic acid (
CHEBI:18237
)
L
-glutamic acid (
CHEBI:16015
)
is a
glutamic acid (
CHEBI:18237
)
glutamate(1−) (
CHEBI:14321
)
is conjugate base of
glutamic acid (
CHEBI:18237
)
α-glutamyl group (
CHEBI:22453
)
is substituent group from
glutamic acid (
CHEBI:18237
)
γ-glutamyl group (
CHEBI:24190
)
is substituent group from
glutamic acid (
CHEBI:18237
)
glutamic acid residue (
CHEBI:32483
)
is substituent group from
glutamic acid (
CHEBI:18237
)
glutamo group (
CHEBI:24321
)
is substituent group from
glutamic acid (
CHEBI:18237
)
glutamoyl group (
CHEBI:24322
)
is substituent group from
glutamic acid (
CHEBI:18237
)
IUPAC Names
2-aminopentanedioic acid
glutamic acid
Synonyms
Sources
2-Aminoglutaric acid
KEGG COMPOUND
DL-Glutamic acid
KEGG DRUG
DL-Glutaminic acid
KEGG COMPOUND
E
ChEBI
Glu
ChEBI
Glutamate
KEGG COMPOUND
Glutamic acid
KEGG COMPOUND
Glutaminic acid
KEGG COMPOUND
Glutaminsäure
ChEBI
Manual Xrefs
Databases
C00001358
KNApSAcK
C00019577
KNApSAcK
C00302
KEGG COMPOUND
D04341
KEGG DRUG
Glutamic_acid
Wikipedia
View more database links
Registry Numbers
Types
Sources
101971
Gmelin Registry Number
Gmelin
1723799
Reaxys Registry Number
Reaxys
617-65-2
CAS Registry Number
ChemIDplus
617-65-2
CAS Registry Number
NIST Chemistry WebBook
Citations
Types
Sources
15739367
PubMed citation
Europe PMC
17190852
PubMed citation
Europe PMC
24616376
PubMed citation
Europe PMC
24984001
PubMed citation
Europe PMC
Last Modified
18 April 2024