Structure Information
Structure

Compound Identification

SMILES

CC1O[C@@H](O[C@@H]2C(CO)O[C@H](C(OC(C)=O)[C@H]2O)C2=C(O)C=C(O)C3=C2OC(=CC3=O)C2=CC=C(O)C=C2)[C@@H](O)C(O)[C@H]1O

InChIKey

InChIKey=YQZCWVJLTIJRST-QJLMMVJWSA-N

Formula

C29H32O15

Mass

620.56

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Phenylpropanoids and polyketides

Class

Flavonoids

Subclass

Flavonoid glycosides

Intermediate Tree Nodes

Flavonoid C-glycosides

Direct Parent

Flavonoid 8-C-glycosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Flavonoid-8-c-glycoside - 4'-hydroxyflavonoid - 5-hydroxyflavonoid - 7-hydroxyflavonoid - Flavone - Hydroxyflavonoid - Phenolic glycoside - C-glycosyl compound - Chromone - Disaccharide - Glycosyl compound - O-glycosyl compound - Benzopyran - 1-benzopyran - 1-hydroxy-2-unsubstituted benzenoid - Pyranone - Phenol - Pyran - Monocyclic benzene moiety - Oxane - Benzenoid - Vinylogous acid - Heteroaromatic compound - Secondary alcohol - Carboxylic acid ester - Acetal - Oxacycle - Ether - Dialkyl ether - Polyol - Carboxylic acid derivative - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Primary alcohol - Carbonyl group - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Alcohol - Organooxygen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as flavonoid 8-c-glycosides. These are compounds containing a carbohydrate moiety which is C-glycosidically linked to 8-position of a 2-phenylchromen-4-one flavonoid backbone.

External Descriptors

LIPIDMAPS (LMPK12110275) : Flavones and Flavonols

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