CHEBI:75741 - (−)-taxifolin 3-O-β-D-xylopyranoside

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ChEBI Name (−)-taxifolin 3-O-β-D-xylopyranoside
ChEBI ID CHEBI:75741
ChEBI ASCII Name (-)-taxifolin 3-O-beta-D-xylopyranoside
Definition A flavanone glycoside that is (−)-taxifolin substituted by a β-D-xylopyranosyl residue at position 3.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C20H20O11
Net Charge 0
Average Mass 436.36620
Monoisotopic Mass 436.10056
InChI InChI=1S/C20H20O11/c21-8-4-11(24)14-13(5-8)30-18(7-1-2-9(22)10(23)3-7)19(16(14)27)31-20-17(28)15(26)12(25)6-29-20/h1-5,12,15,17-26,28H,6H2/t12-,15+,17-,18+,19-,20+/m1/s1
InChIKey UKSPRKDZNYSFRL-HMMBQGTNSA-N
SMILES O[C@@H]1CO[C@@H](O[C@H]2[C@@H](Oc3cc(O)cc(O)c3C2=O)c2ccc(O)c(O)c2)[C@H](O)[C@H]1O
Roles Classification
Biological Role(s): metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
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ChEBI Ontology
Outgoing (−)-taxifolin 3-O-β-D-xylopyranoside (CHEBI:75741) has functional parent β-D-xylose (CHEBI:28161)
(−)-taxifolin 3-O-β-D-xylopyranoside (CHEBI:75741) has functional parent (−)-taxifolin (CHEBI:41963)
(−)-taxifolin 3-O-β-D-xylopyranoside (CHEBI:75741) has role metabolite (CHEBI:25212)
(−)-taxifolin 3-O-β-D-xylopyranoside (CHEBI:75741) is a β-D-xyloside (CHEBI:27926)
(−)-taxifolin 3-O-β-D-xylopyranoside (CHEBI:75741) is a 3'-hydroxyflavanones (CHEBI:48024)
(−)-taxifolin 3-O-β-D-xylopyranoside (CHEBI:75741) is a 4'-hydroxyflavanones (CHEBI:140331)
(−)-taxifolin 3-O-β-D-xylopyranoside (CHEBI:75741) is a flavanone glycoside (CHEBI:72730)
(−)-taxifolin 3-O-β-D-xylopyranoside (CHEBI:75741) is a monosaccharide derivative (CHEBI:63367)
(−)-taxifolin 3-O-β-D-xylopyranoside (CHEBI:75741) is a tetrahydroxyflavanone (CHEBI:38742)
IUPAC Name
(2S,3S)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxo-3,4-dihydro-2H-chromen-3-yl β-D-xylopyranoside
Synonym Source
(2S,3S)-taxifolin 3-O-β-D-xyloside ChEBI
Registry Number Type Source
5783158 Reaxys Registry Number Reaxys
Last Modified
06 April 2018