Structure Information
Structure

Compound Identification

SMILES

COC1=C2C(=O)C(O)=C(OC2=CC(O)=C1O)C1=CC=C(O[C@@H]2OC(C)[C@H](O)C(O)[C@@H]2O)C=C1

InChIKey

InChIKey=COJAFCZHQKNUSI-CHSYGBCRSA-N

Formula

C22H22O11

Mass

462.407

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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-4p-o-glycoside - 5-methoxyflavonoid-skeleton - 3-hydroxyflavone - 3-hydroxyflavonoid - 6-hydroxyflavonoid - 7-hydroxyflavonoid - Hydroxyflavonoid - Flavone - Phenolic glycoside - Fatty acyl glycoside - Fatty acyl glycoside of mono- or disaccharide - Alkyl glycoside - Hexose monosaccharide - Glycosyl compound - Chromone - O-glycosyl compound - Benzopyran - 1-benzopyran - Phenol ether - Anisole - Phenoxy compound - Alkyl aryl ether - 1-hydroxy-2-unsubstituted benzenoid - Pyranone - Pyran - Monocyclic benzene moiety - Monosaccharide - Fatty acyl - Benzenoid - Oxane - Heteroaromatic compound - Vinylogous ester - Secondary alcohol - Ether - Polyol - Oxacycle - Organoheterocyclic compound - Acetal - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Organic oxide - 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 (LMPK12112831) : Flavones and Flavonols

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