Structure Information
Structure

Compound Identification

SMILES

COC1=C(OC)C=C(\C=C\C(=O)C2=C(O)C=CC=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C=C1

InChIKey

InChIKey=NXFQYTVQTDBITH-WLUAWGNHSA-N

Formula

C23H26O10

Mass

462.451

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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 - Linear 1,3-diarylpropanoid - Cinnamylphenol - Phenolic glycoside - Cinnamic acid or derivatives - Hexose monosaccharide - Glycosyl compound - O-glycosyl compound - O-dimethoxybenzene - Dimethoxybenzene - Styrene - Anisole - Phenoxy compound - Phenol ether - Benzoyl - Methoxybenzene - Aryl ketone - Alkyl aryl ether - 1-hydroxy-4-unsubstituted benzenoid - Phenol - 1-hydroxy-2-unsubstituted benzenoid - Monocyclic benzene moiety - Monosaccharide - Oxane - Benzenoid - Alpha,beta-unsaturated ketone - Vinylogous acid - Acryloyl-group - Enone - Ketone - Secondary alcohol - Acetal - Oxacycle - Organoheterocyclic compound - Polyol - Ether - Organic oxygen compound - Hydrocarbon derivative - Alcohol - Primary alcohol - Aldehyde - Organic oxide - 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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