Structure Information
Structure

Compound Identification

SMILES

COC1=CC(OC2O[C@H](CO[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O)[C@@H](O)[C@H](O)[C@H]2O)=CC(OC)=C1C(=O)\C=C\C1=CC(OC)=C(OC)C=C1

InChIKey

InChIKey=ABXVFQMDSBBQME-ARHNCLLPSA-N

Formula

C31H40O15

Mass

652.646

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