|
(2S)-5,7,3',5'-tetrahydroxyflavanone-7-O-β-D-glucopyranoside |
|
CHEBI:66214 |
|
(2S)-5,7,3',5'-tetrahydroxyflavanone-7-O-beta-D-glucopyranoside |
|
A flavanone glycoside that is (2S)-5,7,3',5'-tetrahydroxyflavanone attached to a β-D-glucopyranosyl residue at position 7 via a glycosidic linkage. Isolated from Jasminum lanceolarium, it exhibits radical scavenging activity. |
|
This entity has been manually annotated by the ChEBI Team.
|
|
|
|
Molfile
XML
SDF
|
|
|
|
InChI=1S/C21H22O11/c22-7-16-18(27)19(28)20(29)21(32-16)30-11-4-12(25)17-13(26)6-14(31-15(17)5-11)8-1-9(23)3-10(24)2-8/h1-5,14,16,18-25,27-29H,6-7H2/t14-,16+,18+,19-,20+,21+/m0/s1 |
DCTQXNWQTLOMPD-SFTVRKLSSA-N |
OC[C@H]1O[C@@H](Oc2cc(O)c3C(=O)C[C@H](Oc3c2)c2cc(O)cc(O)c2)[C@H](O)[C@@H](O)[C@@H]1O |
|
Jasminum lanceolarium
(NCBI:txid310427)
|
Found in
stem
(BTO:0001300).
See:
PubMed
|
Jasminum lanceolarium
(NCBI:txid310427)
|
Found in
leaf
(BTO:0000713).
See:
PubMed
|
radical scavenger
A role played by a substance that can react readily with, and thereby eliminate, radicals.
|
|
metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
|
|
View more via ChEBI Ontology
Outgoing
|
(2S)-5,7,3',5'-tetrahydroxyflavanone-7-O-β-D-glucopyranoside
(CHEBI:66214)
has role
metabolite
(CHEBI:25212)
(2S)-5,7,3',5'-tetrahydroxyflavanone-7-O-β-D-glucopyranoside
(CHEBI:66214)
has role
radical scavenger
(CHEBI:48578)
(2S)-5,7,3',5'-tetrahydroxyflavanone-7-O-β-D-glucopyranoside
(CHEBI:66214)
is a
β-D-glucoside
(CHEBI:22798)
(2S)-5,7,3',5'-tetrahydroxyflavanone-7-O-β-D-glucopyranoside
(CHEBI:66214)
is a
flavanone glycoside
(CHEBI:72730)
(2S)-5,7,3',5'-tetrahydroxyflavanone-7-O-β-D-glucopyranoside
(CHEBI:66214)
is a
monosaccharide derivative
(CHEBI:63367)
(2S)-5,7,3',5'-tetrahydroxyflavanone-7-O-β-D-glucopyranoside
(CHEBI:66214)
is a
trihydroxyflavanone
(CHEBI:38739)
|
|
(2S)-2-(3,5-dihydroxyphenyl)-5-hydroxy-4-oxo-3,4-dihydro-2H-chromen-7-yl β-D-glucopyranoside
|
11051130
|
Reaxys Registry Number
|
Reaxys
|
17329896
|
PubMed citation
|
Europe PMC
|
|