Summary

IMPPAT Phytochemical identifier: IMPHY002996

Phytochemical name: Bracteatin 6-glucoside

Synonymous chemical names:
bracteatin 6-glucoside

External chemical identifiers:
CID:42607774

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Chemical structure information

SMILES:
OCC1O[C@@H](Oc2cc3OC(=Cc4cc(O)c(c(c4)O)O)C(=O)c3c(c2)O)C([C@H]([C@@H]1O)O)O

InChI:
InChI=1S/C21H20O12/c22-6-14-18(28)19(29)20(30)21(33-14)31-8-4-9(23)15-12(5-8)32-13(17(15)27)3-7-1-10(24)16(26)11(25)2-7/h1-5,14,18-26,28-30H,6H2/t14?,18-,19+,20?,21-/m1/s1

InChIKey:
SFXSFWVZPKEDPA-YHYCZKRCSA-N

DeepSMILES:
OCCO[C@@H]OcccOC=CcccO)ccc6)O))O))))))C=O)c5cc9)O))))))))))C[C@H][C@@H]6O))O))O

Functional groups:
CO, cC=C1OccC1=O, cO, cO[C@@H](C)OC

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Molecular scaffolds

Scaffold Graph/Node/Bond level:
O=C1C(=Cc2ccccc2)Oc2cc(OC3CCCCO3)ccc21

Scaffold Graph/Node level:
OC1C(CC2CCCCC2)OC2CC(OC3CCCCO3)CCC21

Scaffold Graph level:
CC1C(CC2CCCCC2)CC2CC(CC3CCCCC3)CCC21

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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: Aurones

NP-Likeness score: 1.646

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Chemical structure download