Summary

IMPPAT Phytochemical identifier: IMPHY000845

Phytochemical name: Taxifolin 3-O-beta-D-xylopyranoside

Synonymous chemical names:
taxifolin-3-o-beta-d xylopyranosyl-beta-d-arbinopyranoside

External chemical identifiers:
CID:493319, ChEMBL:CHEMBL2332676, ChEBI:75739, ZINC:ZINC000032066887, MolPort-028-599-885

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Chemical structure information

SMILES:
Oc1cc(O)c2c(c1)O[C@@H]([C@H](C2=O)O[C@@H]1OC[C@H]([C@@H]([C@H]1O)O)O)c1ccc(c(c1)O)O

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-ARLBNVOWSA-N

DeepSMILES:
OcccO)ccc6)O[C@@H][C@H]C6=O))O[C@@H]OC[C@H][C@@H][C@H]6O))O))O)))))))cccccc6)O))O

Functional groups:
CO, CO[C@H](C)OC, cC(C)=O, cO, cOC

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Molecular scaffolds

Scaffold Graph/Node/Bond level:
O=C1c2ccccc2OC(c2ccccc2)C1OC1CCCCO1

Scaffold Graph/Node level:
OC1C2CCCCC2OC(C2CCCCC2)C1OC1CCCCO1

Scaffold Graph level:
CC1C2CCCCC2CC(C2CCCCC2)C1CC1CCCCC1

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Chemical classification

ClassyFire Kingdom: Organic compounds

ClassyFire Superclass: Phenylpropanoids and polyketides

ClassyFire Class: Flavonoids

ClassyFire Subclass: Flavonoid glycosides

NP Classifier Biosynthetic pathway: Shikimates and Phenylpropanoids

NP Classifier Superclass: Flavonoids

NP Classifier Class: Dihydroflavonols

NP-Likeness score: 2.433

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Chemical structure download