Structure Information
Structure

Compound Identification

SMILES

COC1=C(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C=CC(=C1)C(=O)\C=C\C1=CC=C(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C=C1

InChIKey

InChIKey=CCMBJKVXNYVZBT-CVFSNQCTSA-N

Formula

C28H34O14

Mass

594.566

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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 - Retrochalcone - Fatty acyl glycoside - Phenolic glycoside - Fatty acyl glycoside of mono- or disaccharide - Linear 1,3-diarylpropanoid - Alkyl glycoside - Cinnamic acid or derivatives - Glycosyl compound - O-glycosyl compound - Phenoxy compound - Anisole - Benzoyl - Methoxybenzene - Phenol ether - Styrene - Aryl ketone - Alkyl aryl ether - Oxane - Benzenoid - Fatty acyl - Monosaccharide - Monocyclic benzene moiety - Acryloyl-group - Alpha,beta-unsaturated ketone - Enone - Ketone - Secondary alcohol - Polyol - Organoheterocyclic compound - Acetal - Oxacycle - Ether - Primary alcohol - Organooxygen compound - Hydrocarbon derivative - Alcohol - Organic oxygen compound - Organic oxide - Aldehyde - 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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