Structure Information
Structure

Compound Identification

SMILES

CC(C)C1(O)C(CO)OC(OC2=CC=CC=C2)C(O)(OC2OC(CO)C(O)C(O)C2O)C1O

InChIKey

InChIKey=CLEXUMAQDPYDCU-UHFFFAOYSA-N

Formula

C21H32O12

Mass

476.475

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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

O-glycosyl compounds Disaccharides Phenoxy compounds Phenol ethers Oxanes Tertiary alcohols Secondary alcohols Hemiacetals Polyols Oxacyclic compounds Acetals Primary alcohols Hydrocarbon derivatives

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Phenolic glycoside - Disaccharide - O-glycosyl compound - Phenoxy compound - Phenol ether - Monocyclic benzene moiety - Oxane - Benzenoid - Tertiary alcohol - Hemiacetal - Secondary alcohol - Polyol - Organoheterocyclic compound - Oxacycle - Acetal - Primary alcohol - Alcohol - 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

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