Structure Information
Structure

Compound Identification

SMILES

COC1=C(O)C=C(C=C1O[C@@H]1OC[C@@H](O)C(O)C1O)C1=C(OC)C(=O)C2=C(O)C=C(O)C=C2O1

InChIKey

InChIKey=OEFVQTLECRIMST-ODCKNITQSA-N

Formula

C22H22O12

Mass

478.406

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Phenylpropanoids and polyketides

Class

Flavonoids

Subclass

Flavonoid glycosides

Intermediate Tree Nodes

Not available

Direct Parent

Flavonoid O-glycosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Flavonoid o-glycoside - Flavonoid-3p-o-glycoside - 3-methoxyflavonoid-skeleton - 4p-methoxyflavonoid-skeleton - Hydroxyflavonoid - 3'-hydroxyflavonoid - Flavone - 5-hydroxyflavonoid - 7-hydroxyflavonoid - Phenolic glycoside - 3-methoxychromone - O-glycosyl compound - Glycosyl compound - Chromone - 1-benzopyran - Benzopyran - Methoxyphenol - Phenol ether - Phenoxy compound - Anisole - Methoxybenzene - 1-hydroxy-2-unsubstituted benzenoid - 1-hydroxy-4-unsubstituted benzenoid - Pyranone - Alkyl aryl ether - Phenol - Monocyclic benzene moiety - Benzenoid - Pyran - Monosaccharide - Oxane - Heteroaromatic compound - Vinylogous acid - Secondary alcohol - Oxacycle - Organoheterocyclic compound - Acetal - Polyol - Ether - Hydrocarbon derivative - Alcohol - Organic oxygen compound - Organooxygen compound - Organic oxide - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as flavonoid o-glycosides. These are compounds containing a carbohydrate moiety which is O-glycosidically linked to the 2-phenylchromen-4-one flavonoid backbone.

External Descriptors

LIPIDMAPS (LMPK12112785) : Flavones and Flavonols

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