Structure Information
Structure

Compound Identification

SMILES

CC1=C(O)C(C(=O)C=CC2=CC(O)=CC=C2)=C(O)C(C)=C1OC1OC(C(O)C(O)C1O)C(O)=O

InChIKey

InChIKey=DMTBDEGNVXIAEQ-UHFFFAOYSA-N

Formula

C23H24O11

Mass

476.434

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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'-hydroxychalcone - Phenolic glycoside - Linear 1,3-diarylpropanoid - Cinnamylphenol - 1-o-glucuronide - O-glucuronide - Glucuronic acid or derivatives - Hexose monosaccharide - Hydroxycinnamic acid or derivatives - Glycosyl compound - O-glycosyl compound - Xylenol - Benzoyl - Phenoxy compound - M-xylene - Xylene - O-cresol - P-cresol - Phenol ether - Resorcinol - Styrene - Aryl ketone - Phenol - Beta-hydroxy acid - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Benzenoid - Oxane - Monocyclic benzene moiety - Pyran - Monosaccharide - Hydroxy acid - Alpha,beta-unsaturated ketone - Vinylogous acid - Enone - Acryloyl-group - Secondary alcohol - Ketone - Carboxylic acid - Monocarboxylic acid or derivatives - Polyol - Carboxylic acid derivative - Oxacycle - Organoheterocyclic compound - Acetal - Alcohol - Hydrocarbon derivative - Carbonyl group - Organooxygen compound - Organic oxygen compound - Organic oxide - 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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