Structure Information
Structure

Compound Identification

SMILES

OC1C(O)C(OC2=CC(O)=CC3=C2C(OS(O)(=O)=O)C(C(=O)C3=O)C2=C(O)C=C(O)C3=C2C(O)C(=O)C=C3O)OC(C1O)C(O)=O

InChIKey

InChIKey=RAXFWRUUSVQZJN-UHFFFAOYSA-N

Formula

C26H22O19S

Mass

670.5

Export to:

JSON SDF CSV

Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organic oxygen compounds

Class

Organooxygen compounds

Subclass

Carbohydrates and carbohydrate conjugates

Intermediate Tree Nodes

Glycosyl compounds

Direct Parent

Phenolic glycosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Phenolic glycoside - O-glucuronide - 1-o-glucuronide - Glucuronic acid or derivatives - Naphthoquinone - O-glycosyl compound - 1-naphthol - Tetralin - Naphthalene - Aryl ketone - Quinone - 1-hydroxy-2-unsubstituted benzenoid - Beta-hydroxy acid - Benzenoid - Sulfuric acid ester - Alkyl sulfate - Sulfate-ester - Sulfuric acid monoester - Pyran - Oxane - Monosaccharide - Hydroxy acid - Vinylogous acid - Organic sulfuric acid or derivatives - Cyclic ketone - Secondary alcohol - Ketone - Oxacycle - Organoheterocyclic compound - Polyol - Monocarboxylic acid or derivatives - Enol - Carboxylic acid - Carboxylic acid derivative - Acetal - Organic oxide - Hydrocarbon derivative - Carbonyl group - Alcohol - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose.

External Descriptors

Not available

Previous Back Next