Structure Information
Structure

Compound Identification

SMILES

NC(C(O)=O)C1=CC=C(OC2OC(CO)C(O)C(O)C2OC2OC(CO)C(O)C(O)C2O)C=C1

InChIKey

InChIKey=PHPOPZGUOBMSPZ-UHFFFAOYSA-N

Formula

C20H29NO13

Mass

491.446

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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 - Disaccharide - O-glycosyl compound - Alpha-amino acid - Alpha-amino acid or derivatives - Phenoxy compound - Phenol ether - Aralkylamine - Monocyclic benzene moiety - Oxane - Benzenoid - Secondary alcohol - Amino acid or derivatives - Amino acid - Oxacycle - Organoheterocyclic compound - Polyol - Acetal - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Carboxylic acid - Primary amine - Organic oxide - Primary aliphatic amine - Organonitrogen compound - Carbonyl group - Alcohol - Hydrocarbon derivative - Amine - Organopnictogen compound - Organic nitrogen compound - Primary alcohol - 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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