Structure Information
Structure

Compound Identification

SMILES

CC1=C(O)C2=C(O[C@@H](CC2=O)C2=CC=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)C=C2)C(C)=C1O

InChIKey

InChIKey=MFYKJSBELPBPGQ-UZLUQKTDSA-N

Formula

C23H26O10

Mass

462.451

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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-hydroxyflavonoid - 7-hydroxyflavonoid - Hydroxyflavonoid - Flavanone - Flavan - Phenolic glycoside - Fatty acyl glycoside of mono- or disaccharide - Fatty acyl glycoside - Alkyl glycoside - Hexose monosaccharide - O-glycosyl compound - Glycosyl compound - Chromone - Benzopyran - Chromane - 1-benzopyran - Phenoxy compound - Aryl alkyl ketone - Aryl ketone - Phenol ether - Alkyl aryl ether - Oxane - Monosaccharide - Monocyclic benzene moiety - Fatty acyl - Benzenoid - Vinylogous acid - Ketone - Secondary alcohol - Organoheterocyclic compound - Ether - Oxacycle - Acetal - Polyol - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Organic oxide - Alcohol - Aldehyde - 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

Not available

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