Structure Information
Structure

Compound Identification

SMILES

CC(C)(C1=CC=C(OCC2=CC=CC(COC3=CC=C(C=C3)C(N)=N)=C2)C=C1)C1=CC=C(O[C@@H]2O[C@@H]([C@@H](O)[C@H](O)[C@H]2O)C(O)=O)C=C1

InChIKey

InChIKey=FIMQVXNJBFDOAA-RSENBJTISA-N

Formula

C36H38N2O9

Mass

642.705

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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

Fatty acyl glycoside of mono- or disaccharide - Phenolic glycoside - Fatty acyl glycoside - 1-o-glucuronide - O-glucuronide - Glucuronic acid or derivatives - Diphenylmethane - Hexose monosaccharide - Alkyl glycoside - O-glycosyl compound - Phenylpropane - Phenol ether - Phenoxy compound - Alkyl aryl ether - Beta-hydroxy acid - Benzenoid - Monocyclic benzene moiety - Pyran - Monosaccharide - Oxane - Hydroxy acid - Fatty acyl - Secondary alcohol - Acetal - Amidine - Carboxylic acid amidine - Carboxylic acid derivative - Carboxylic acid - Oxacycle - Ether - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Polyol - Carboximidamide - Alcohol - Organic oxide - Hydrocarbon derivative - Carbonyl group - Organic nitrogen compound - Organonitrogen compound - Organopnictogen 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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