Structure Information
Structure

Compound Identification

SMILES

CC1O[C@@H](OC2[C@@H](O)[C@H](O)C(CO)O[C@H]2C2=C(O)C=C(O)C3=C2OC(=CC3=O)C2=CC=C(O[C@@H]3OC(CO)[C@@H](O)C(O)C3O)C=C2)C(O)[C@@H](O)[C@H]1O

InChIKey

InChIKey=LJDOSKINEPZMJE-OKNFIAIGSA-N

Formula

C33H40O19

Mass

740.664

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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 - Flavonoid-8-c-glycoside - Flavonoid c-glycoside - Flavone - 5-hydroxyflavonoid - 7-hydroxyflavonoid - Hydroxyflavonoid - Phenolic glycoside - Fatty acyl glycoside of mono- or disaccharide - Fatty acyl glycoside - Alkyl glycoside - C-glycosyl compound - Chromone - Glycosyl compound - Disaccharide - O-glycosyl compound - Benzopyran - 1-benzopyran - Phenoxy compound - Phenol ether - Pyranone - 1-hydroxy-2-unsubstituted benzenoid - Oxane - Pyran - Benzenoid - Fatty acyl - Monocyclic benzene moiety - Heteroaromatic compound - Vinylogous acid - Secondary alcohol - Ether - Dialkyl ether - Organoheterocyclic compound - Oxacycle - Acetal - Polyol - Primary alcohol - Organic oxide - Organic oxygen compound - Hydrocarbon derivative - Alcohol - Organooxygen compound - 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 (LMPK12110299) : Flavones and Flavonols

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