Structure Information
Structure

Compound Identification

SMILES

COC1=CC(OC)=C(OC)C=C1C1=COC2=C(C(O)=CC(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)=C2OC)C1=O

InChIKey

InChIKey=VDIAQGCUYKTVQT-KNGJJONBSA-N

Formula

C25H28O13

Mass

536.486

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Phenylpropanoids and polyketides

Class

Isoflavonoids

Subclass

Isoflavonoid O-glycosides

Intermediate Tree Nodes

Not available

Direct Parent

Isoflavonoid O-glycosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Isoflavonoid o-glycoside - Isoflavonoid-7-o-glycoside - 3p-methoxyisoflavone - 4p-o-methylisoflavone - Hydroxyisoflavonoid - Isoflavone - Phenolic glycoside - Hexose monosaccharide - Chromone - Glycosyl compound - O-glycosyl compound - Benzopyran - 1-benzopyran - Phenoxy compound - Anisole - Methoxybenzene - Phenol ether - Pyranone - Alkyl aryl ether - 1-hydroxy-2-unsubstituted benzenoid - Benzenoid - Pyran - Monocyclic benzene moiety - Monosaccharide - Oxane - Heteroaromatic compound - Vinylogous acid - Secondary alcohol - Acetal - Oxacycle - Ether - Organoheterocyclic compound - Polyol - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Alcohol - Primary alcohol - Organooxygen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as isoflavonoid o-glycosides. These are o-glycosylated derivatives of isoflavonoids, which are natural products derived from 3-phenylchromen-4-one.

External Descriptors

Not available

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