Structure Information
Structure

Compound Identification

SMILES

CC1O[C@@H](OC2C(O)[C@H](O)C(CO)O[C@H]2OC2=C(O)C=C(C=C2)C2=CC(=O)C3=C(O)C=C(O)C=C3O2)[C@@H](O)C(O)[C@H]1O

InChIKey

InChIKey=SUDIELTVVOYEKB-OKGGZUOPSA-N

Formula

C27H30O15

Mass

594.522

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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 heteropolycyclic compounds

Substituents

Flavonoid o-glycoside - Flavonoid-4p-o-glycoside - 3'-hydroxyflavonoid - 5-hydroxyflavonoid - 7-hydroxyflavonoid - Hydroxyflavonoid - Flavone - Phenolic glycoside - Fatty acyl glycoside of mono- or disaccharide - Fatty acyl glycoside - Alkyl glycoside - Chromone - O-glycosyl compound - Glycosyl compound - Disaccharide - Benzopyran - 1-benzopyran - Phenoxy compound - Phenol ether - Phenol - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Pyranone - Oxane - Pyran - Benzenoid - Monocyclic benzene moiety - Fatty acyl - Vinylogous acid - Heteroaromatic compound - Secondary alcohol - Polyol - Acetal - Organoheterocyclic compound - Oxacycle - Organic oxygen compound - Alcohol - Organooxygen compound - Organic oxide - Hydrocarbon derivative - Primary alcohol - Aromatic heteropolycyclic 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 (LMPK12110674) : Flavones and Flavonols

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