Structure Information
Structure

Compound Identification

SMILES

OCC1OC(OC2=C(O)C(=CC=C2)C(=O)OC2C(O)[C@H](O)C(CO)O[C@H]2O[C@@H]2OC=C3[C@@H](CCOC3=O)[C@H]2C=C)C(O)C(O)C1O

InChIKey

InChIKey=XYZDSXRSOLCDDD-GYCHHVCBSA-N

Formula

C29H36O17

Mass

656.59

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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-hydroxybenzoic acid ester - O-glycosyl compound - Salicylic acid or derivatives - Benzoate ester - Benzoic acid or derivatives - Benzoyl - Phenoxy compound - Phenol ether - Delta valerolactone - Delta_valerolactone - Sugar acid - 1-hydroxy-4-unsubstituted benzenoid - Phenol - Monocyclic benzene moiety - Dicarboxylic acid or derivatives - Benzenoid - Monosaccharide - Oxane - Vinylogous ester - Vinylogous acid - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Lactone - Carboxylic acid ester - Secondary alcohol - Acetal - Carboxylic acid derivative - Organoheterocyclic compound - Oxacycle - Polyol - Alcohol - Carbonyl group - Hydrocarbon derivative - Organic oxide - Primary 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

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