Structure Information
Structure

Compound Identification

SMILES

OC[C@H]1O[C@@H](OC2=C(OC3=CC(O)=CC(O)=C3C2=O)C2=CC(OS([O-])(=O)=O)=C(O)C=C2)[C@H](O)[C@@H](O)[C@@H]1O

InChIKey

InChIKey=YXZPJASIVFGNHX-QSOFNFLRSA-M

Formula

C21H19O15S

Mass

543.43

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Phenylpropanoids and polyketides

Class

Flavonoids

Subclass

Flavonoid glycosides

Intermediate Tree Nodes

Flavonoid O-glycosides

Direct Parent

Flavonoid-3-O-glycosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Flavonoid-3-o-glycoside - Hydroxyflavonoid - 4'-hydroxyflavonoid - 5-hydroxyflavonoid - Flavone - 7-hydroxyflavonoid - Hexose monosaccharide - Phenylsulfate - O-glycosyl compound - Glycosyl compound - Chromone - Arylsulfate - 1-benzopyran - Benzopyran - Phenoxy compound - 1-hydroxy-2-unsubstituted benzenoid - 1-hydroxy-4-unsubstituted benzenoid - Pyranone - Phenol - Monocyclic benzene moiety - Benzenoid - Monosaccharide - Sulfuric acid ester - Oxane - Sulfate-ester - Sulfuric acid monoester - Pyran - Organic sulfuric acid or derivatives - Vinylogous acid - Heteroaromatic compound - Secondary alcohol - Acetal - Organoheterocyclic compound - Oxacycle - Polyol - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Alcohol - Organic oxygen compound - Primary alcohol - Organic anion - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as flavonoid-3-o-glycosides. These are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C3-position.

External Descriptors

Not available

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