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Structure Information
Structure

Compound Identification

SMILES

O[C@H]1[C@H](OC2=CC=CC(C=CC(O)=O)=C2)O[C@@H]([C@@H](O)[C@@H]1O)C(O)=O

InChIKey

InChIKey=XPCHMFOWDFTFNV-DKBOKBLXSA-N

Formula

C15H16O9

Mass

340.284

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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 heteromonocyclic compounds

Substituents

Phenolic glycoside - 1-o-glucuronide - O-glucuronide - Glucuronic acid or derivatives - Cinnamic acid - Cinnamic acid or derivatives - Coumaric acid or derivatives - Hexose monosaccharide - O-glycosyl compound - Styrene - Phenoxy compound - Phenol ether - Beta-hydroxy acid - Oxane - Pyran - Monosaccharide - Hydroxy acid - Monocyclic benzene moiety - Dicarboxylic acid or derivatives - Benzenoid - Secondary alcohol - Polyol - Organoheterocyclic compound - Oxacycle - Acetal - Carboxylic acid - Carboxylic acid derivative - Hydrocarbon derivative - Carbonyl group - Alcohol - Organic oxide - 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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