Structure Information
Structure

Compound Identification

SMILES

CC1=C(O)C(C(=O)CCC2=CC=C(OC3OC(C(O)C(O)C3O)C(O)=O)C=C2)=C(O)C(C)=C1O

InChIKey

InChIKey=RSDRJJSXDKVLJY-UHFFFAOYSA-N

Formula

C23H26O11

Mass

478.45

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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 heteromonocyclic compounds

Substituents

Flavonoid o-glycoside - 2'-hydroxy-dihydrochalcone - Cinnamylphenol - Linear 1,3-diarylpropanoid - Phenolic glycoside - O-glucuronide - 1-o-glucuronide - Alkyl-phenylketone - Glucuronic acid or derivatives - Acylphloroglucinol derivative - Butyrophenone - O-glycosyl compound - Glycosyl compound - Benzenetriol - Phenylketone - Xylenol - Phloroglucinol derivative - Phenoxy compound - Benzoyl - M-xylene - Xylene - O-cresol - P-cresol - Phenol ether - Aryl alkyl ketone - Aryl ketone - Beta-hydroxy acid - Phenol - Benzenoid - Pyran - Oxane - Monocyclic benzene moiety - Hydroxy acid - Monosaccharide - Vinylogous acid - Ketone - Secondary alcohol - Polyol - Organoheterocyclic compound - Oxacycle - Carboxylic acid - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Acetal - Organooxygen compound - Organic oxide - Organic oxygen compound - Carbonyl group - Alcohol - Hydrocarbon derivative - Aromatic heteromonocyclic 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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