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InChI=1S/CH4O/c1-2/h2H,1H3
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ChEBI
> Main
CHEBI:9380 - syringin
Main
ChEBI Ontology
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ChEBI Name
syringin
ChEBI ID
CHEBI:9380
Definition
A monosaccharide derivative that is
trans
-sinapyl alcohol attached to a β-
D
-glucopyranosyl residue at position 1 via a glycosidic linkage.
Stars
This entity has been manually annotated by the ChEBI Team.
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Wikipedia
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Read full article at Wikipedia
Formula
C17H24O9
Net Charge
0
Average Mass
372.36706
Monoisotopic Mass
372.14203
InChI
InChI=1S/C17H24O9/c1-
23-
10-
6-
9(4-
3-
5-
18)
7-
11(24-
2)
16(10)
26-
17-
15(22)
14(21)
13(20)
12(8-
19)
25-
17/h3-
4,6-
7,12-
15,17-
22H,5,8H2,1-
2H3/b4-
3+/t12-
,13-
,14+,15-
,17+/m1/s1
InChIKey
QJVXKWHHAMZTBY-GCPOEHJPSA-N
SMILES
COc1cc(cc(OC)c1O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)\C=C\CO
Roles Classification
Biological Role
(s):
plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
apoptosis inducer
Any substance that induces the process of apoptosis (programmed cell death) in multi-celled organisms.
autophagy inducer
Any compound that induces the process of autophagy (the self-digestion of one or more components of a cell through the action of enzymes originating within the same cell).
Application
(s):
hepatoprotective agent
Any compound that is able to prevent damage to the liver.
anti-inflammatory agent
Any compound that has anti-inflammatory effects.
neuroprotective agent
Any compound that can be used for the treatment of neurodegenerative disorders.
antidepressant
Antidepressants are mood-stimulating drugs used primarily in the treatment of affective disorders and related conditions.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
syringin (
CHEBI:9380
)
has functional parent
trans
-sinapyl alcohol (
CHEBI:64557
)
syringin (
CHEBI:9380
)
has role
anti-inflammatory agent (
CHEBI:67079
)
syringin (
CHEBI:9380
)
has role
antidepressant (
CHEBI:35469
)
syringin (
CHEBI:9380
)
has role
apoptosis inducer (
CHEBI:68495
)
syringin (
CHEBI:9380
)
has role
autophagy inducer (
CHEBI:138880
)
syringin (
CHEBI:9380
)
has role
hepatoprotective agent (
CHEBI:62868
)
syringin (
CHEBI:9380
)
has role
neuroprotective agent (
CHEBI:63726
)
syringin (
CHEBI:9380
)
has role
plant metabolite (
CHEBI:76924
)
syringin (
CHEBI:9380
)
is a
β-
D
-glucoside (
CHEBI:22798
)
syringin (
CHEBI:9380
)
is a
dimethoxybenzene (
CHEBI:51681
)
syringin (
CHEBI:9380
)
is a
monosaccharide derivative (
CHEBI:63367
)
syringin (
CHEBI:9380
)
is a
primary alcohol (
CHEBI:15734
)
IUPAC Name
4-[(1
E
)-3-hydroxyprop-1-en-1-yl]-2,6-dimethoxyphenyl β-
D
-glucopyranoside
Synonyms
Sources
(
E
)-sinapyl alcohol 4-glucoside
ChEBI
4-[(1
E
)-3-hydroxy-1-propen-1-yl]-2,6-dimethoxyphenyl β-
D
-glucopyranoside
ChEBI
4-
O
-(β-
D
-glucosyl)-
trans
-4-sinapoyl alcohol
UniProt
beta-Terpineol
ChemIDplus
eleutheroside B
KEGG COMPOUND
eleutheroside B
ChemIDplus
ligustrin
ChemIDplus
lilacin
ChemIDplus
magnolenin A
ChemIDplus
methoxyconiferine
ChemIDplus
syrigin
ChemIDplus
syringenin
ChemIDplus
syringin
KEGG COMPOUND
syringoside
ChemIDplus
Manual Xrefs
Databases
C00000010
KNApSAcK
C01533
KEGG COMPOUND
CPD-63
MetaCyc
FDB011657
FooDB
Syringin
Wikipedia
View more database links
Registry Numbers
Types
Sources
118-34-3
CAS Registry Number
KEGG COMPOUND
118-34-3
CAS Registry Number
ChemIDplus
97166
Reaxys Registry Number
Reaxys
Citations
Types
Sources
23620140
PubMed citation
Europe PMC
23666001
PubMed citation
Europe PMC
23678812
PubMed citation
Europe PMC
31661774
PubMed citation
Europe PMC
33867336
PubMed citation
Europe PMC
34658231
PubMed citation
Europe PMC
35580997
PubMed citation
Europe PMC
35598514
PubMed citation
Europe PMC
35706960
PubMed citation
Europe PMC
35794555
PubMed citation
Europe PMC
36411652
PubMed citation
Europe PMC
36840496
PubMed citation
Europe PMC
37243678
PubMed citation
Europe PMC
37278329
PubMed citation
Europe PMC
37882327
PubMed citation
Europe PMC
38212029
PubMed citation
Europe PMC
38520788
PubMed citation
Europe PMC
38611823
PubMed citation
Europe PMC
Last Modified
07 May 2024