Structure Information
Structure

Compound Identification

SMILES

CO[C@@H]1[C@H](O)[C@@H](O)[C@@H](NC(=O)C(\C)=C/C2=CC(O)=C(O[C@@H]3O[C@@H]([C@@H](O)[C@@H]3O)C(C)=O)C=C2)[C@@H](O)[C@@H]1OC

InChIKey

InChIKey=JBVRFSABBMBGGN-GGMQGACSSA-N

Formula

C24H33NO12

Mass

527.523

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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 - Hydroxycinnamic acid or derivatives - Cinnamic acid amide - Cinnamic acid or derivatives - O-glycosyl compound - Pentose monosaccharide - Phenoxy compound - Phenol ether - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Cyclohexanol - Monosaccharide - Cyclitol or derivatives - Monocyclic benzene moiety - Benzenoid - Cyclic alcohol - Tetrahydrofuran - Carboxamide group - Ketone - Secondary alcohol - Secondary carboxylic acid amide - Acetal - Carboxylic acid derivative - Oxacycle - Organoheterocyclic compound - Polyol - Dialkyl ether - Ether - Alcohol - Hydrocarbon derivative - Organic nitrogen compound - Organopnictogen compound - Carbonyl group - Organic oxide - Organonitrogen compound - 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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