Structure Information
Structure

Compound Identification

SMILES

OCC1OC(OC2=C(O)C=C3C[C@H](N(C(=O)\C=C\C4=CC=C(O)C=C4)C3=C2)C(O)=O)C(O)C(O)C1O

InChIKey

InChIKey=VICXKBPMEPRWFK-RWOIVYKOSA-N

Formula

C24H25NO11

Mass

503.46

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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 - N-acyl-l-alpha-amino acid - Indolecarboxylic acid derivative - Indolecarboxylic acid - Hydroxycinnamic acid or derivatives - Hexose monosaccharide - Coumaric acid or derivatives - Cinnamic acid or derivatives - O-glycosyl compound - Alpha-amino acid or derivatives - Indole or derivatives - Styrene - Phenol - 1-hydroxy-2-unsubstituted benzenoid - Oxane - Benzenoid - Monosaccharide - Monocyclic benzene moiety - Tertiary carboxylic acid amide - Secondary alcohol - Carboxamide group - Acetal - Carboxylic acid derivative - Carboxylic acid - Oxacycle - Azacycle - Organoheterocyclic compound - Polyol - Monocarboxylic acid or derivatives - Organic nitrogen compound - Hydrocarbon derivative - Organopnictogen compound - Carbonyl group - Primary alcohol - Organic oxide - Organonitrogen compound - Alcohol - 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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