Structure Information
Structure

Compound Identification

SMILES

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

InChIKey

InChIKey=QJTYCCFDQWFJHU-WNZLTNKYSA-N

Formula

C21H20O12

Mass

464.379

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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-5-o-glycoside - 3-hydroxyflavone - Hydroxyflavonoid - 3'-hydroxyflavonoid - Flavone - 7-hydroxyflavonoid - 4'-hydroxyflavonoid - 3-hydroxyflavonoid - Phenolic glycoside - Hexose monosaccharide - O-glycosyl compound - Chromone - Glycosyl compound - 1-benzopyran - Benzopyran - Catechol - Pyranone - Phenol - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Monocyclic benzene moiety - Oxane - Monosaccharide - Pyran - Benzenoid - Heteroaromatic compound - Vinylogous ester - Secondary alcohol - Organoheterocyclic compound - Oxacycle - Acetal - Polyol - Primary alcohol - Organic oxide - Alcohol - Organic oxygen compound - 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

Not available

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