Structure Information
Structure

Compound Identification

SMILES

OCC1O[C@@H](OC2[C@@H](O)[C@H](O)C(CO)O[C@H]2OC2=CC(O)=C3C(=O)C(=COC3=C2)C2=CC(O)=C(O)C=C2)C(O)[C@@H](O)[C@@H]1O

InChIKey

InChIKey=VGMFHMLQOYWYHN-IBSAKFLHSA-N

Formula

C27H30O16

Mass

610.521

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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-7-o-glycoside - Isoflavonoid o-glycoside - Hydroxyisoflavonoid - Isoflavone - Phenolic glycoside - O-glycosyl compound - Glycosyl compound - Chromone - Disaccharide - Benzopyran - 1-benzopyran - Catechol - Pyranone - 1-hydroxy-4-unsubstituted benzenoid - Phenol - 1-hydroxy-2-unsubstituted benzenoid - Pyran - Oxane - Monocyclic benzene moiety - Benzenoid - Vinylogous acid - Heteroaromatic compound - Secondary alcohol - Acetal - Oxacycle - Organoheterocyclic compound - Polyol - Alcohol - Hydrocarbon derivative - Organic oxide - Primary alcohol - Organic oxygen compound - 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

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