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ChEBI
> Main
CHEBI:5525 - gossypin
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ChEBI Ontology
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ChEBI Name
gossypin
ChEBI ID
CHEBI:5525
Definition
A glycosyloxyflavone that is gossypetin attached to a β-
D
-glucopyranosyl residue at position 8 via a glycosidic linkage.
Stars
This entity has been manually annotated by the ChEBI Team.
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Formula
C21H20O13
Net Charge
0
Average Mass
480.37570
Monoisotopic Mass
480.09039
InChI
InChI=1S/C21H20O13/c22-
5-
11-
13(27)
15(29)
17(31)
21(32-
11)
34-
19-
10(26)
4-
9(25)
12-
14(28)
16(30)
18(33-
20(12)
19)
6-
1-
2-
7(23)
8(24)
3-
6/h1-
4,11,13,15,17,21-
27,29-
31H,5H2/t11-
,13-
,15+,17-
,21+/m1/s1
InChIKey
SJRXVLUZMMDCNG-KKPQBLLMSA-N
SMILES
OC[C@H]1O[C@@H](Oc2c(O)cc(O)c3c2oc(-c2ccc(O)c(O)c2)c(O)c3=O)[C@H](O)[C@@H](O)[C@@H]1O
Metabolite of Species
Details
Fioria vitifolia
(NCBI:txid183231)
See:
PubMed
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.
Application
(s):
neuroprotective agent
Any compound that can be used for the treatment of neurodegenerative disorders.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
gossypin (
CHEBI:5525
)
has functional parent
gossypetin (
CHEBI:16400
)
gossypin (
CHEBI:5525
)
has role
neuroprotective agent (
CHEBI:63726
)
gossypin (
CHEBI:5525
)
has role
plant metabolite (
CHEBI:76924
)
gossypin (
CHEBI:5525
)
is a
7-hydroxyflavonol (
CHEBI:52267
)
gossypin (
CHEBI:5525
)
is a
glycosyloxyflavone (
CHEBI:50018
)
gossypin (
CHEBI:5525
)
is a
monosaccharide derivative (
CHEBI:63367
)
gossypin (
CHEBI:5525
)
is a
pentahydroxyflavone (
CHEBI:25883
)
IUPAC Name
2-
(3,4-
dihydroxyphenyl)-
3,5,7-
trihydroxy-
4-
oxo-
4
H
-
1-
benzopyran-
8-
yl β-
D
-
glucopyranoside
Synonyms
Sources
3,5,7,8,3',4'-Hexahydroxyflavone-8-glucoside
ChemIDplus
Gossypetin 8-O-glucoside
KEGG COMPOUND
Manual Xrefs
Databases
C00005690
KNApSAcK
C10051
KEGG COMPOUND
LSM-36969
LINCS
View more database links
Registry Numbers
Types
Sources
652-78-8
CAS Registry Number
ChemIDplus
71526
Reaxys Registry Number
Reaxys
Citations
Types
Sources
23543365
PubMed citation
Europe PMC
23738444
PubMed citation
Europe PMC
24347764
PubMed citation
Europe PMC
Last Modified
26 February 2016