Structure Information
Structure

Compound Identification

SMILES

CC(=O)NC1=C(Cl)C=CC(CO[C@@H]2O[C@H](COC(=O)C3=CC=CC=C3)[C@@H](O[C@H]3O[C@@H]4CO[C@H](O[C@H]4[C@H](O)[C@H]3O)C3=CC=NC=C3)[C@H](O)[C@H]2O)=C1

InChIKey

InChIKey=VSXUVMKQOMZCFP-HDWSCIHBSA-N

Formula

C34H37ClN2O13

Mass

717.12

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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

O-glycosyl compounds

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

O-glycosyl compound - O-haloacetanilide - Haloacetanilide - Disaccharide - Acetanilide - Pyranodioxin - Benzoate ester - N-acetylarylamine - Anilide - Benzoic acid or derivatives - Benzoyl - N-arylamide - Chlorobenzene - Halobenzene - Oxane - Benzenoid - Aryl chloride - Pyridine - Aryl halide - Meta-dioxane - Monocyclic benzene moiety - Heteroaromatic compound - Acetamide - Carboxamide group - Carboxylic acid ester - Secondary alcohol - Secondary carboxylic acid amide - Oxacycle - Azacycle - Acetal - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Organoheterocyclic compound - Organohalogen compound - Organochloride - Organic nitrogen compound - Hydrocarbon derivative - Alcohol - Carbonyl group - Organonitrogen compound - Organopnictogen compound - Organic oxide - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond.

External Descriptors

Not available

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