Structure Information
Structure

Compound Identification

SMILES

OC[C@@H]1O[C@@H](OC2=C(C=C(O)C=C2)C(=O)NC2=C(C=C(O)C=C2)C(O)=O)[C@@H](O)[C@H](O)[C@H]1O

InChIKey

InChIKey=UQULZPHAPMSIMX-SAGLZJIZSA-N

Formula

C20H21NO11

Mass

451.384

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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 - O-glycosyl compound - Hydroxybenzoic acid - Benzamide - 4-alkoxyphenol - Benzoic acid - Benzoic acid or derivatives - Phenoxy compound - Benzoyl - Phenol ether - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Monosaccharide - Benzenoid - Oxane - Monocyclic benzene moiety - Vinylogous amide - Carboxamide group - Secondary carboxylic acid amide - Secondary alcohol - Acetal - Oxacycle - Organoheterocyclic compound - Carboxylic acid derivative - Carboxylic acid - Polyol - Monocarboxylic acid or derivatives - Alcohol - Organic nitrogen compound - Organopnictogen compound - Primary alcohol - Organic oxide - Hydrocarbon derivative - 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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