Structure Information
Structure

Compound Identification

SMILES

CC1=C(O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)C=CC2=C1OC(=O)C=C2C1=CC=CC=C1

InChIKey

InChIKey=RHTBSKLRGSELHW-XJESJRCUSA-N

Formula

C22H22O8

Mass

414.41

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Phenylpropanoids and polyketides

Class

Neoflavonoids

Subclass

Neoflavonoid 7-O-glycosides

Intermediate Tree Nodes

Not available

Direct Parent

Neoflavonoid 7-O-glycosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Neoflavonoid-7-o-glycoside - Coumarin-7-o-glycoside - Coumarin o-glycoside - 4-phenylcoumarin - Phenolic glycoside - Hexose monosaccharide - Coumarin - Glycosyl compound - O-glycosyl compound - Benzopyran - 1-benzopyran - Pyranone - Oxane - Pyran - Monocyclic benzene moiety - Benzenoid - Monosaccharide - Heteroaromatic compound - Secondary alcohol - Lactone - Polyol - Organoheterocyclic compound - Oxacycle - Acetal - 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 neoflavonoid 7-o-glycosides. These are 7-O-glycosylated neoflavonoids. Neoflavonoids are compounds with a structure based on the 4-phenylchromene backbone.

External Descriptors

Not available

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