Structure Information
Structure

Compound Identification

SMILES

CC(=O)OC1=CC(O)=C2C(OC(=C(O)C2=O)C2=CC(O[C@@H]3OC(CO)[C@@H](O)[C@H](O)C3O)=C(O)C=C2)=C1

InChIKey

InChIKey=YPRSSMIANKNTIN-DKAYPGPQSA-N

Formula

C23H22O13

Mass

506.416

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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-hydroxyflavone - Hydroxyflavonoid - 3-hydroxyflavonoid - 4'-hydroxyflavonoid - 5-hydroxyflavonoid - Flavone - Phenolic glycoside - Hexose monosaccharide - O-glycosyl compound - Glycosyl compound - Chromone - Benzopyran - 1-benzopyran - Phenoxy compound - Phenol ether - Pyranone - Phenol - 1-hydroxy-2-unsubstituted benzenoid - 1-hydroxy-4-unsubstituted benzenoid - Benzenoid - Oxane - Monocyclic benzene moiety - Monosaccharide - Pyran - Heteroaromatic compound - Vinylogous acid - Secondary alcohol - Carboxylic acid ester - Polyol - Organoheterocyclic compound - Carboxylic acid derivative - Oxacycle - Acetal - Monocarboxylic acid or derivatives - Primary alcohol - Organic oxide - Carbonyl group - Organic oxygen compound - Alcohol - 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 (LMPK12112224) : Flavones and Flavonols

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