Structure Information
Structure

Compound Identification

SMILES

COC1=C(OC2=CC(O)=CC(O)=C2C1=O)C1=CC(O)=C(O)C(O[C@@H]2OC(CO)[C@@H](O)C(O)C2O)=C1

InChIKey

InChIKey=BWVLOICUZVJWAO-OSYQZDLNSA-N

Formula

C22H22O13

Mass

494.405

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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-3p-o-glycoside - Flavonoid o-glycoside - 3-methoxyflavonoid-skeleton - Hydroxyflavonoid - Flavone - 7-hydroxyflavonoid - 5-hydroxyflavonoid - 4'-hydroxyflavonoid - 3'-hydroxyflavonoid - Phenolic glycoside - 3-methoxychromone - Hexose monosaccharide - Glycosyl compound - O-glycosyl compound - Chromone - 1-benzopyran - Benzopyran - Catechol - Phenol ether - Phenoxy compound - Phenol - 1-hydroxy-2-unsubstituted benzenoid - Alkyl aryl ether - 1-hydroxy-4-unsubstituted benzenoid - Pyranone - Monosaccharide - Oxane - Benzenoid - Monocyclic benzene moiety - Pyran - Heteroaromatic compound - Vinylogous acid - Secondary alcohol - Polyol - Organoheterocyclic compound - Acetal - Oxacycle - Ether - Primary alcohol - Organic oxide - Alcohol - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - 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 (LMPK12112775) : Flavones and Flavonols

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