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ChEBI
> Main
CHEBI:136713 -
N
-oleoyl-
L
-glutamic acid
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ChEBI Name
N
-oleoyl-
L
-glutamic acid
ChEBI ID
CHEBI:136713
ChEBI ASCII Name
N-oleoyl-L-glutamic acid
Definition
A fatty amide resulting from the formal condensation of the carboxy group of oleic acid with the amino group of
L
-glutamic acid.
Stars
This entity has been manually annotated by the ChEBI Team.
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Formula
C23H41NO5
Net Charge
0
Average Mass
411.576
Monoisotopic Mass
411.29847
InChI
InChI=1S/C23H41NO5/c1-
2-
3-
4-
5-
6-
7-
8-
9-
10-
11-
12-
13-
14-
15-
16-
17-
21(25)
24-
20(23(28)
29)
18-
19-
22(26)
27/h9-
10,20H,2-
8,11-
19H2,1H3,(H,24,25)
(H,26,27)
(H,28,29)
/b10-
9-
/t20-
/m0/s1
InChIKey
UUFVSGRELDGPGL-QJRAZLAKSA-N
SMILES
C(\CCCCCCCC(=O)N[C@H](C(O)=O)CCC(=O)O)=C\CCCCCCCC
Roles Classification
Chemical Role
(s):
Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Br
o
nsted base).
(via
oxoacid
)
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
N
-oleoyl-
L
-glutamic acid (
CHEBI:136713
)
has functional parent
oleic acid (
CHEBI:16196
)
N
-oleoyl-
L
-glutamic acid (
CHEBI:136713
)
is a
N
-(fatty acyl)-
L
-α-amino acid (
CHEBI:137550
)
N
-oleoyl-
L
-glutamic acid (
CHEBI:136713
)
is a
N
-acyl-
L
-glutamic acid (
CHEBI:21650
)
N
-oleoyl-
L
-glutamic acid (
CHEBI:136713
)
is conjugate acid of
N
-oleoyl-
L
-glutamate(2−) (
CHEBI:134122
)
Incoming
N
-oleoyl-
L
-glutamate(2−) (
CHEBI:134122
)
is conjugate base of
N
-oleoyl-
L
-glutamic acid (
CHEBI:136713
)
IUPAC Name
N
-[(9
Z
)-octadec-9-enoyl]-
L
-glutamic acid
Synonyms
Sources
(2
S
)-2-{[(9
Z
)-octadec-9-enoyl]amino}pentanedioic acid
ChEBI
N-(9Z-octadecenoyl)-glutamic acid
LIPID MAPS
N
-(9
Z
-octadecenoyl)-
L
-glutamic acid
ChEBI
N
-(9
Z
-octadecenoyl)glutamic acid
ChEBI
N
-[(9
Z
)-octadecenoyl]-
L
-glutamic acid
ChEBI
N
-[(9
Z
)-octadecenoyl]glutamic acid
ChEBI
N-oleoyl glutamic acid
LIPID MAPS
N
-oleoylglutamic acid
ChEBI
Oleoyl glutamic acid
ChemIDplus
oleoylglutamic acid
ChEBI
Manual Xref
Database
LMFA08020088
LIPID MAPS
View more database links
Registry Numbers
Types
Sources
1717063
Reaxys Registry Number
Reaxys
4627-61-6
CAS Registry Number
ChemIDplus
Citation
Type
Source
27374330
PubMed citation
Europe PMC
Last Modified
27 June 2017