Structure Information
Structure

Compound Identification

SMILES

COC1=CC2=C(C=C1)C(=O)C(=CO2)C1=CC=C(OC2OC(CO)C(O)C(O)C2O)C=C1

InChIKey

InChIKey=YAYJWUXAGVZHGX-UHFFFAOYSA-N

Formula

C22H22O9

Mass

430.409

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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-4p-o-glycoside - 7-o-methylisoflavone - Isoflavone - Fatty acyl glycoside - Phenolic glycoside - Fatty acyl glycoside of mono- or disaccharide - Alkyl glycoside - Hexose monosaccharide - Chromone - Glycosyl compound - O-glycosyl compound - Benzopyran - 1-benzopyran - Phenoxy compound - Anisole - Phenol ether - Pyranone - Alkyl aryl ether - Monosaccharide - Fatty acyl - Pyran - Benzenoid - Monocyclic benzene moiety - Oxane - Heteroaromatic compound - Secondary alcohol - Organoheterocyclic compound - Oxacycle - Acetal - Ether - Polyol - Primary alcohol - Organic oxide - Organic oxygen compound - Hydrocarbon derivative - 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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