Structure Information
Structure

Compound Identification

SMILES

OCC1OC(Oc2cccc(O)c2C(=O)OCc2ccccc2OC2OC(COC(=O)c3ccccc3)C(O)C(O)C2O)C(O)C(O)C1O

InChIKey

InChIKey=ISOTWRKLHJHVEB-UHFFFAOYSA-N

Formula

C33H36O16

Mass

688.635

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 heteromonocyclic compounds

Substituents

Phenolic glycoside - O-hydroxybenzoic acid ester - O-glycosyl compound - Benzyloxycarbonyl - Benzoate ester - Salicylic acid or derivatives - Benzoic acid or derivatives - Phenoxy compound - Phenol ether - Benzoyl - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Sugar acid - Monocyclic benzene moiety - Dicarboxylic acid or derivatives - Monosaccharide - Oxane - Benzenoid - Vinylogous acid - Carboxylic acid ester - Secondary alcohol - Acetal - Oxacycle - Organoheterocyclic compound - Carboxylic acid derivative - Polyol - Alcohol - Primary alcohol - Organic oxide - Hydrocarbon derivative - Aromatic heteromonocyclic 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