Structure Information
Structure

Compound Identification

SMILES

COC1=C(OC(C)=O)C2=C(C(O)=C1)C(=O)C(O[C@@H]1O[C@@H](C)[C@H](O)[C@@H](O)[C@H]1O)=C(O2)C1=CC(O)=C(O)C=C1

InChIKey

InChIKey=XCQNRWMPPLJRCM-PZSVWFBASA-N

Formula

C24H24O13

Mass

520.443

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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

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