Structure Information
Structure

Compound Identification

SMILES

C[C@H]1O[C@@H](OC[C@@H]2O[C@@H](OC3=CC(=CC=C3O)C3=CC(=O)C4=C(O3)C=C(OS(O)(=O)=O)C=C4O)[C@@H](O)[C@H](O)[C@@H]2O)[C@H](O)[C@@H](O)[C@H]1O

InChIKey

InChIKey=XEPFWJSKSWCFRK-QIZHAKPKSA-N

Formula

C27H30O18S

Mass

674.58

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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-3p-o-glycoside - Hydroxyflavonoid - Flavone - 5-hydroxyflavonoid - 4'-hydroxyflavonoid - Phenolic glycoside - O-glycosyl compound - Glycosyl compound - Disaccharide - Chromone - Arylsulfate - 1-benzopyran - Benzopyran - Phenoxy compound - Phenol ether - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Pyranone - Phenol - Benzenoid - Sulfuric acid ester - Sulfate-ester - Sulfuric acid monoester - Pyran - Oxane - Monocyclic benzene moiety - Heteroaromatic compound - Vinylogous acid - Organic sulfuric acid or derivatives - Secondary alcohol - Oxacycle - Organoheterocyclic compound - Polyol - Acetal - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - 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

Not available

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