Structure Information
Structure

Compound Identification

SMILES

COC1=C(O[C@@H]2OC(CO)[C@@H](O)[C@H](O)C2O)C=C(C=C1)C1=CC(=O)C2=C(O)C([C@H]3C[C@@H](O)[C@@H](O)C(C)O3)=C(O)C=C2O1

InChIKey

InChIKey=UAGXUOZTLLGXAK-TUBSJWQLSA-N

Formula

C28H32O14

Mass

592.55

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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 - Flavonoid c-glycoside - 4p-methoxyflavonoid-skeleton - Flavone - 5-hydroxyflavonoid - 7-hydroxyflavonoid - Hydroxyflavonoid - Phenolic glycoside - Glycosyl compound - Chromone - O-glycosyl compound - 1-benzopyran - Benzopyran - Methoxybenzene - Phenol ether - Phenoxy compound - Anisole - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Alkyl aryl ether - Pyranone - Monocyclic benzene moiety - Benzenoid - Oxane - Pyran - Monosaccharide - Heteroaromatic compound - Vinylogous acid - Secondary alcohol - Ether - Dialkyl ether - Organoheterocyclic compound - Oxacycle - Acetal - Polyol - Primary alcohol - Organic oxide - 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 (LMPK12110809) : Flavones and Flavonols

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