Structure Information
Structure

Compound Identification

SMILES

COC1=CC=C(C=C1)C1=C(O[C@H]2O[C@@H](C)[C@H](OC(C)=O)[C@@H](CO[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@H]2O)C(=O)C2=C(O1)C(CC=C(C)C)=C(O)C=C2O

InChIKey

InChIKey=YXQNIHHKJSDXTM-PVDHIVFCSA-N

Formula

C36H44O16

Mass

732.732

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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

8-prenylated flavone - Flavonoid-3-o-glycoside - 4p-methoxyflavonoid-skeleton - Hydroxyflavonoid - Flavone - 5-hydroxyflavonoid - 7-hydroxyflavonoid - O-glycosyl compound - Glycosyl compound - Chromone - Benzopyran - 1-benzopyran - Phenoxy compound - Phenol ether - Anisole - Methoxybenzene - 1-hydroxy-2-unsubstituted benzenoid - Pyranone - Alkyl aryl ether - Benzenoid - Monocyclic benzene moiety - Pyran - Monosaccharide - Oxane - Heteroaromatic compound - Vinylogous acid - Secondary alcohol - Carboxylic acid ester - Acetal - Ether - Oxacycle - Carboxylic acid derivative - Organoheterocyclic compound - Polyol - Monocarboxylic acid or derivatives - Organic oxygen compound - Carbonyl group - Organooxygen compound - Alcohol - Primary alcohol - Hydrocarbon derivative - Organic oxide - 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

Not available

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