Structure Information
Structure

Compound Identification

SMILES

COC1=C(O[C@@H]2OC(CO)[C@@H](O)[C@H](O)C2O)C(O)=C2C(=O)C(OC)=C(OC2=C1)C1=CC(O)=C(O)C=C1

InChIKey

InChIKey=QSJCBTMNXPAKKC-DKDGADBKSA-N

Formula

C23H24O13

Mass

508.432

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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-6-o-glycoside - Flavonoid o-glycoside - 3-methoxyflavonoid-skeleton - 7-methoxyflavonoid-skeleton - 3'-hydroxyflavonoid - 4'-hydroxyflavonoid - 5-hydroxyflavonoid - Flavone - Hydroxyflavonoid - Phenolic glycoside - 3-methoxychromone - Hexose monosaccharide - Chromone - Glycosyl compound - O-glycosyl compound - Benzopyran - 1-benzopyran - Anisole - Catechol - Pyranone - Phenol - Alkyl aryl ether - 1-hydroxy-2-unsubstituted benzenoid - 1-hydroxy-4-unsubstituted benzenoid - Oxane - Pyran - Monosaccharide - Benzenoid - Monocyclic benzene moiety - Vinylogous acid - Heteroaromatic compound - Secondary alcohol - Oxacycle - Organoheterocyclic compound - Polyol - Acetal - Ether - Organooxygen compound - Alcohol - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Primary alcohol - 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 (LMPK12112920) : Flavones and Flavonols

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