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> Main
CHEBI:68986 - luteolin-4'-
O
-β-
D
-glucopyranoside
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ChEBI Name
luteolin-4'-
O
-β-
D
-glucopyranoside
ChEBI ID
CHEBI:68986
ChEBI ASCII Name
luteolin-4'-O-beta-D-glucopyranoside
Definition
A glycosyloxyflavone that is luteolin substituted by a β-
D
-glucopyranosyl residue at position 4' via a glycosidic linkage. It has been isolated from
Olea europaea
.
Stars
This entity has been manually annotated by the ChEBI Team.
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Formula
C21H20O11
Net Charge
0
Average Mass
448.37690
Monoisotopic Mass
448.10056
InChI
InChI=1S/C21H20O11/c22-
7-
16-
18(27)
19(28)
20(29)
21(32-
16)
31-
13-
2-
1-
8(3-
10(13)
24)
14-
6-
12(26)
17-
11(25)
4-
9(23)
5-
15(17)
30-
14/h1-
6,16,18-
25,27-
29H,7H2/t16-
,18-
,19+,20-
,21-
/m1/s1
InChIKey
UHNXUSWGOJMEFO-QNDFHXLGSA-N
SMILES
OC[C@H]1O[C@@H](Oc2ccc(cc2O)-c2cc(=O)c3c(O)cc(O)cc3o2)[C@H](O)[C@@H](O)[C@@H]1O
Metabolite of Species
Details
Olea europaea
(NCBI:txid4146)
Found in leaf
(BTO:0000713)
. Methanolic and aqueous extract of dried olive leaves 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.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
luteolin-4'-
O
-β-
D
-glucopyranoside (
CHEBI:68986
)
has functional parent
luteolin (
CHEBI:15864
)
luteolin-4'-
O
-β-
D
-glucopyranoside (
CHEBI:68986
)
has role
plant metabolite (
CHEBI:76924
)
luteolin-4'-
O
-β-
D
-glucopyranoside (
CHEBI:68986
)
is a
β-
D
-glucoside (
CHEBI:22798
)
luteolin-4'-
O
-β-
D
-glucopyranoside (
CHEBI:68986
)
is a
glycosyloxyflavone (
CHEBI:50018
)
luteolin-4'-
O
-β-
D
-glucopyranoside (
CHEBI:68986
)
is a
monosaccharide derivative (
CHEBI:63367
)
luteolin-4'-
O
-β-
D
-glucopyranoside (
CHEBI:68986
)
is a
trihydroxyflavone (
CHEBI:27116
)
IUPAC Name
4-
(5,7-
dihydroxy-
4-
oxo-
4
H
-
1-
benzopyran-
2-
yl)-
2-
hydroxyphenyl β-
D
-
glucopyranoside
Synonym
Source
5,7,3'-trihydroxyflavone 4'-
O
-β-
D
-glucopyranoside
ChEBI
Registry Number
Type
Source
65285
Reaxys Registry Number
Reaxys
Citation
Type
Source
22014168
PubMed citation
Europe PMC
Last Modified
05 June 2015