Structure Information
Structure

Compound Identification

SMILES

[H][C@@]1(CO)O[C@]([H])(OC2=CC(OC)=CC3=C2C(=O)C=C(O3)C2=CC(OC)=C(O)C=C2)[C@@]([H])(O)[C@]([H])(O)[C@]1([H])O

InChIKey

InChIKey=UHLWPBYBTUVRPB-QZUCXDRTSA-N

Formula

C23H24O11

Mass

476.434

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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-5-o-glycoside - Flavonoid o-glycoside - 3p-methoxyflavonoid-skeleton - 7-methoxyflavonoid-skeleton - Flavone - 4'-hydroxyflavonoid - Monohydroxyflavonoid - Hydroxyflavonoid - Phenolic glycoside - Hexose monosaccharide - Chromone - O-glycosyl compound - Glycosyl compound - Benzopyran - Methoxyphenol - 1-benzopyran - Methoxybenzene - Anisole - Phenoxy compound - Phenol ether - 1-hydroxy-2-unsubstituted benzenoid - Alkyl aryl ether - Pyranone - Phenol - Pyran - Benzenoid - Monosaccharide - Monocyclic benzene moiety - Oxane - Heteroaromatic compound - Vinylogous ester - Secondary alcohol - Acetal - Oxacycle - Organoheterocyclic compound - Polyol - Ether - Hydrocarbon derivative - Organic oxide - Primary alcohol - Organic oxygen compound - Organooxygen compound - 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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