Structure Information
Structure

Compound Identification

SMILES

C[N+]1([O-])[C@H]2CC[C@@H]1CC(C2)OC(C1=CC=CC=C1)C1=CC=C(O[C@@H]2OC([C@@H](O)[C@H](O)[C@H]2O)C(O)=O)C=C1

InChIKey

InChIKey=VWBJEBJNNLKRKO-AWBXFYKNSA-N

Formula

C27H33NO9

Mass

515.559

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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 heteropolycyclic compounds

Substituents

Phenolic glycoside - Fatty acyl glycoside - Fatty acyl glycoside of mono- or disaccharide - 1-o-glucuronide - O-glucuronide - Diphenylmethane - Glucuronic acid or derivatives - Alkyl glycoside - O-glycosyl compound - Benzylether - Tropane alkaloid - Phenoxy compound - Phenol ether - Beta-hydroxy acid - Monocyclic benzene moiety - Hydroxy acid - Monosaccharide - Fatty acyl - Oxane - Benzenoid - Piperidine - Pyran - N-alkylpyrrolidine - Pyrrolidine - Trialkyl amine oxide - Secondary alcohol - Trisubstituted n-oxide - Polyol - Acetal - Carboxylic acid derivative - Carboxylic acid - Dialkyl ether - Ether - Oxacycle - Azacycle - Monocarboxylic acid or derivatives - Organoheterocyclic compound - N-oxide - Organic salt - Carbonyl group - Hydrocarbon derivative - Organopnictogen compound - Organic zwitterion - Alcohol - Organic nitrogen compound - Organonitrogen compound - Organic oxide - Aromatic heteropolycyclic 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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