Structure Information
Structure

Compound Identification

SMILES

CC1=C(O)C(C(=O)CCC2=CC=C(O)C=C2)=C(O)C(C)=C1OC1OC(C(O)C(O)C1O)C(O)=O

InChIKey

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