Structure Information
Structure

Compound Identification

SMILES

COC1=CC(O)=C2C(=O)C(O[C@@H]3OC(CO[C@@H]4OCC(O)(CO)[C@@H]4O)[C@@H](O)[C@H](O[C@@H]4OC(C)[C@H](O)C(O)[C@@H]4O)C3O)=C(OC2=C1)C1=CC=C(O)C=C1

InChIKey

InChIKey=ORQXPQKGHOWSDB-KPGRKQHDSA-N

Formula

C33H40O19

Mass

740.664

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Phenylpropanoids and polyketides

Class

Flavonoids

Subclass

Flavonoid glycosides

Intermediate Tree Nodes

Flavonoid O-glycosides

Direct Parent

Flavonoid-3-O-glycosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Oligosaccharide - Flavonoid-3-o-glycoside - 7-methoxyflavonoid-skeleton - 4'-hydroxyflavonoid - 5-hydroxyflavonoid - Flavone - Hydroxyflavonoid - Chromone - Glycosyl compound - O-glycosyl compound - Benzopyran - 1-benzopyran - Anisole - 1-hydroxy-2-unsubstituted benzenoid - Pyranone - Alkyl aryl ether - Phenol - 1-hydroxy-4-unsubstituted benzenoid - Benzenoid - Pyran - Monocyclic benzene moiety - Oxane - Tertiary alcohol - Oxolane - Heteroaromatic compound - Vinylogous acid - Secondary alcohol - Ether - Polyol - Oxacycle - Organoheterocyclic compound - Acetal - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Primary alcohol - Alcohol - Organic oxygen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as flavonoid-3-o-glycosides. These are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C3-position.

External Descriptors

LIPIDMAPS (LMPK12112581) : Flavones and Flavonols

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