Structure Information
Structure

Compound Identification

SMILES

OC[C@H]1OC(OC2=C(O)C=CC(=C2)C2=CC(=O)C3=C(O)C=C(OS(O)(=O)=O)C=C3O2)[C@H](O)[C@@H](O)[C@@H]1O

InChIKey

InChIKey=OTZOUMPODICORE-MKJMBMEGSA-N

Formula

C21H20O14S

Mass

528.44

Export to:

JSON SDF CSV

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 - 4'-hydroxyflavonoid - 5-hydroxyflavonoid - Flavone - Phenolic glycoside - Hexose monosaccharide - O-glycosyl compound - Glycosyl compound - Chromone - Arylsulfate - Benzopyran - 1-benzopyran - Phenoxy compound - Phenol ether - Phenol - 1-hydroxy-4-unsubstituted benzenoid - Pyranone - 1-hydroxy-2-unsubstituted benzenoid - Monosaccharide - Sulfuric acid ester - Benzenoid - Sulfate-ester - Monocyclic benzene moiety - Pyran - Oxane - Sulfuric acid monoester - Heteroaromatic compound - Vinylogous acid - Organic sulfuric acid or derivatives - Secondary alcohol - Organoheterocyclic compound - Oxacycle - Polyol - 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 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

Previous Back Next