Structure Information
Structure

Compound Identification

SMILES

CC(C)=CCC1=C(O[C@@H]2OC(CO)[C@@H](O)[C@H](O)C2O)C=CC(C(=O)\C=C\C2=CC=C(O)C=C2)=C1O

InChIKey

InChIKey=HNRQFWQDRYQVNP-QTOWGEKLSA-N

Formula

C26H30O9

Mass

486.517

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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 - 3-prenylated chalcone - 2'-hydroxychalcone - Linear 1,3-diarylpropanoid - Cinnamylphenol - Fatty acyl glycoside of mono- or disaccharide - Phenolic glycoside - Fatty acyl glycoside - Hexose monosaccharide - Hydroxycinnamic acid or derivatives - Alkyl glycoside - Cinnamic acid or derivatives - Glycosyl compound - O-glycosyl compound - Aryl ketone - Phenol ether - Benzoyl - Phenoxy compound - Styrene - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Benzenoid - Oxane - Monosaccharide - Fatty acyl - Monocyclic benzene moiety - Alpha,beta-unsaturated ketone - Vinylogous acid - Enone - Acryloyl-group - Secondary alcohol - Ketone - Polyol - Organoheterocyclic compound - Oxacycle - Acetal - Alcohol - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Aldehyde - Organooxygen compound - Primary alcohol - 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

LIPIDMAPS (LMPK12120030) : Chalcones and dihydrochalcones

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