Structure Information
Structure

Compound Identification

SMILES

COC(=O)C1=C(NC(=O)C2=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)C=CC(O)=C2)C=CC(O)=C1OC

InChIKey

InChIKey=SIEMSGVHIQLEBF-RMZWBFLNSA-N

Formula

C22H25NO12

Mass

495.437

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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

Benzanilide - Phenolic glycoside - Aromatic anilide - Hexose monosaccharide - M-hydroxybenzoic acid ester - O-methoxybenzoic acid or derivatives - O-glycosyl compound - Benzoate ester - Methoxyphenol - Benzamide - 4-alkoxyphenol - Benzoic acid or derivatives - Methoxyaniline - Benzoyl - Methoxybenzene - Phenol ether - Phenoxy compound - Anisole - Alkyl aryl ether - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Monocyclic benzene moiety - Monosaccharide - Benzenoid - Oxane - Vinylogous amide - Methyl ester - Secondary carboxylic acid amide - Carboxylic acid ester - Carboxamide group - Secondary alcohol - Acetal - Monocarboxylic acid or derivatives - Organoheterocyclic compound - Oxacycle - Ether - Carboxylic acid derivative - Polyol - Organonitrogen compound - Organopnictogen compound - Organic oxide - Alcohol - Organic nitrogen compound - Primary 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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