Structure Information
Structure

Compound Identification

SMILES

C[C@@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)[C@H](CO)OC2OC2=CC(O)=C(C(=O)CCC3=CC=C(O)C=C3)C(O)=C2)[C@H](O)[C@H](O)[C@H]1O

InChIKey

InChIKey=CWBZAESOUBENAP-UEOJRISESA-N

Formula

C27H34O14

Mass

582.555

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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'-hydroxy-dihydrochalcone - Fatty acyl glycoside - Fatty acyl glycoside of mono- or disaccharide - Phenolic glycoside - Linear 1,3-diarylpropanoid - Cinnamylphenol - Alkyl-phenylketone - Alkyl glycoside - Butyrophenone - Disaccharide - Glycosyl compound - O-glycosyl compound - Phenylketone - Phenoxy compound - Benzoyl - Phenol ether - Resorcinol - Aryl alkyl ketone - Aryl ketone - Phenol - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Monocyclic benzene moiety - Benzenoid - Oxane - Fatty acyl - Vinylogous acid - Secondary alcohol - Ketone - Acetal - Organoheterocyclic compound - Polyol - Oxacycle - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organooxygen compound - Aldehyde - Alcohol - 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

Not available

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