Structure Information
Structure

Compound Identification

SMILES

CS(=O)(=O)CC(=O)NC1=CC=C(OC2OC(CO)C(O)C(O)C2O)C=C1

InChIKey

InChIKey=BJDAYGMALSZAAU-UHFFFAOYSA-N

Formula

C15H21NO9S

Mass

391.39

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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 - Hexose monosaccharide - O-glycosyl compound - Anilide - Phenoxy compound - N-arylamide - Phenol ether - Monocyclic benzene moiety - Monosaccharide - Oxane - Benzenoid - Sulfonyl - Sulfone - Carboxamide group - Secondary carboxylic acid amide - Secondary alcohol - Acetal - Carboxylic acid derivative - Oxacycle - Organoheterocyclic compound - Polyol - Hydrocarbon derivative - Organic oxide - Alcohol - Organopnictogen compound - Organonitrogen compound - Organosulfur compound - Organic nitrogen compound - Primary alcohol - Carbonyl group - 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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