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Structure Information
Structure

Compound Identification

SMILES

[Na+].CC(=O)NC1=CC=C(O[C@@H]2O[C@@H]([C@@H](O)[C@H](O)[C@H]2O)C([O-])=O)C=C1

InChIKey

InChIKey=OINXIJJEOMGKPB-CYRSAHDMSA-M

Formula

C14H16NNaO8

Mass

349.271

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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 - O-glucuronide - 1-o-glucuronide - Glucuronic acid or derivatives - Hexose monosaccharide - O-glycosyl compound - Acetanilide - N-acetylarylamine - Anilide - Phenol ether - Phenoxy compound - N-arylamide - Beta-hydroxy acid - Monosaccharide - Pyran - Monocyclic benzene moiety - Benzenoid - Oxane - Hydroxy acid - Acetamide - Secondary carboxylic acid amide - Secondary alcohol - Carboxamide group - Carboxylic acid salt - Polyol - Carboxylic acid derivative - Organoheterocyclic compound - Acetal - Monocarboxylic acid or derivatives - Organic alkali metal salt - Oxacycle - Carboxylic acid - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Organic sodium salt - Organic salt - Organonitrogen compound - Carbonyl group - Organic oxide - Organopnictogen compound - Organic cation - 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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