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> Main
CHEBI:16254 - 11-
cis
-retinyl palmitate
Main
ChEBI Ontology
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ChEBI Name
11-
cis
-retinyl palmitate
ChEBI ID
CHEBI:16254
ChEBI ASCII Name
11-cis-retinyl palmitate
Definition
The 11-
cis
-isomer of retinyl palmitate.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:729, CHEBI:11313, CHEBI:19121
Supplier Information
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Formula
C36H60O2
Net Charge
0
Average Mass
524.86040
Monoisotopic Mass
524.45933
InChI
InChI=1S/C36H60O2/c1-
7-
8-
9-
10-
11-
12-
13-
14-
15-
16-
17-
18-
19-
25-
35(37)
38-
30-
28-
32(3)
23-
20-
22-
31(2)
26-
27-
34-
33(4)
24-
21-
29-
36(34,5)
6/h20,22-
23,26-
28H,7-
19,21,24-
25,29-
30H2,1-
6H3/b23-
20-
,27-
26+,31-
22+,32-
28+
InChIKey
VYGQUTWHTHXGQB-SXFSSFKVSA-N
SMILES
CCCCCCCCCCCCCCCC(=O)OC\C=C(C)\C=C/C=C(C)/C=C/C1=C(C)CCCC1(C)C
Metabolite of Species
Details
Homo sapiens
(NCBI:txid9606)
See:
PubMed
Roles Classification
Chemical Role
(s):
antioxidant
A substance that opposes oxidation or inhibits reactions brought about by dioxygen or peroxides.
(via
retinyl palmitate
)
Biological Role
(s):
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (
Homo sapiens
).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
11-
cis
-retinyl palmitate (
CHEBI:16254
)
has functional parent
11-
cis
-retinol (
CHEBI:16302
)
11-
cis
-retinyl palmitate (
CHEBI:16254
)
has role
human metabolite (
CHEBI:77746
)
11-
cis
-retinyl palmitate (
CHEBI:16254
)
is a
11-
cis
-retinyl ester (
CHEBI:195358
)
11-
cis
-retinyl palmitate (
CHEBI:16254
)
is a
retinyl palmitate (
CHEBI:15040
)
IUPAC Name
(2
E
,4
Z
,6
E
,8
E
)-
3,7-
dimethyl-
9-
(2,6,6-
trimethylcyclohex-
1-
en-
1-
yl)nona-
2,4,6,8-
tetraen-
1-
yl hexadecanoate
Synonyms
Sources
11-
cis
-retinyl hexadecanoate
UniProt
11-cis-retinyl palmitate
ChEBI
11-cis-Retinyl palmitate
KEGG COMPOUND
Manual Xrefs
Databases
C03455
KEGG COMPOUND
HMDB0060338
HMDB
LMPR01090052
LIPID MAPS
View more database links
Citations
Types
Sources
3793734
PubMed citation
Europe PMC
3875178
PubMed citation
Europe PMC
Last Modified
24 January 2019