Summary

IMPPAT Phytochemical identifier: IMPHY006615

Phytochemical name: Taxifolin 4'-glucoside

Synonymous chemical names:
dihydroquercetin-4'-monoglucoside

External chemical identifiers:
CID:71587141, ZINC:ZINC000206169740, FDASRS:7CE5093NYZ

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Chemical structure information

SMILES:
OC[C@H]1O[C@@H](Oc2ccc(cc2O)[C@H]2Oc3cc(O)cc(c3C(=O)[C@@H]2O)O)[C@@H]([C@H]([C@@H]1O)O)O

InChI:
InChI=1S/C21H22O12/c22-6-13-15(26)17(28)19(30)21(33-13)32-11-2-1-7(3-9(11)24)20-18(29)16(27)14-10(25)4-8(23)5-12(14)31-20/h1-5,13,15,17-26,28-30H,6H2/t13-,15-,17+,18+,19-,20-,21-/m1/s1

InChIKey:
JLLGHNNPZQRLOQ-JUIPTLLLSA-N

DeepSMILES:
OC[C@H]O[C@@H]Occcccc6O)))[C@H]OcccO)ccc6C=O)[C@@H]%10O))))O)))))))))))))[C@@H][C@H][C@@H]6O))O))O

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

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Molecular scaffolds

Scaffold Graph/Node/Bond level:
O=C1CC(c2ccc(OC3CCCCO3)cc2)Oc2ccccc21

Scaffold Graph/Node level:
OC1CC(C2CCC(OC3CCCCO3)CC2)OC2CCCCC12

Scaffold Graph level:
CC1CC(C2CCC(CC3CCCCC3)CC2)CC2CCCCC12

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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: 2.455

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Chemical structure download