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> Main
CHEBI:80486 - phlorizin chalcone
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ChEBI Name
phlorizin chalcone
ChEBI ID
CHEBI:80486
Definition
A monosaccharide derivative that is
trans
-chalcone substituted by hydroxy groups at positions 4, 4' and 6 and a β-
D
-glucopyranosyloxy group at position 2' respectively.
Stars
This entity has been manually annotated by the ChEBI Team.
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Formula
C21H22O10
Net Charge
0
Average Mass
434.39340
Monoisotopic Mass
434.12130
InChI
InChI=1S/C21H22O10/c22-
9-
16-
18(27)
19(28)
20(29)
21(31-
16)
30-
15-
8-
12(24)
7-
14(26)
17(15)
13(25)
6-
3-
10-
1-
4-
11(23)
5-
2-
10/h1-
8,16,18-
24,26-
29H,9H2/b6-
3+/t16-
,18-
,19+,20-
,21-
/m1/s1
InChIKey
WQCWELFQKXIPCN-JSYAWONVSA-N
SMILES
OC[C@H]1O[C@@H](Oc2cc(O)cc(O)c2C(=O)\C=C\c2ccc(O)cc2)[C@H](O)[C@@H](O)[C@@H]1O
Metabolite of Species
Details
Corylopsis coreana
(NCBI:txid292912)
See:
PubMed
Acacia saligna
(NCBI:txid420411)
See:
PubMed
Roles Classification
Chemical Role
(s):
antioxidant
A substance that opposes oxidation or inhibits reactions brought about by dioxygen or peroxides.
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
phlorizin chalcone (
CHEBI:80486
)
has functional parent
trans
-chalcone (
CHEBI:48965
)
phlorizin chalcone (
CHEBI:80486
)
has role
antioxidant (
CHEBI:22586
)
phlorizin chalcone (
CHEBI:80486
)
has role
plant metabolite (
CHEBI:76924
)
phlorizin chalcone (
CHEBI:80486
)
is a
β-
D
-glucoside (
CHEBI:22798
)
phlorizin chalcone (
CHEBI:80486
)
is a
chalcones (
CHEBI:23086
)
phlorizin chalcone (
CHEBI:80486
)
is a
monosaccharide derivative (
CHEBI:63367
)
phlorizin chalcone (
CHEBI:80486
)
is a
resorcinols (
CHEBI:33572
)
IUPAC Name
3,5-
dihydroxy-
2-
[(2
E
)-
3-
(4-
hydroxyphenyl)prop-
2-
enoyl]phenyl β-
D
-
glucopyranoside
Synonyms
Sources
Chalcone 2'-O-glucoside
KEGG COMPOUND
Isosalipurposide
KNApSAcK
Manual Xrefs
Databases
C00007881
KNApSAcK
C16406
KEGG COMPOUND
LMPK12120250
LIPID MAPS
View more database links
Registry Numbers
Types
Sources
100179
Reaxys Registry Number
Reaxys
4547-85-7
CAS Registry Number
ChemIDplus
Citations
Types
Sources
25183120
PubMed citation
Europe PMC
26028482
PubMed citation
Europe PMC
Last Modified
05 June 2015