Structure Information
Structure

Compound Identification

SMILES

OC(O)C1=NC(=CC(C=CN2C(CC3=C2C=C(O)C(O[C@@H]2O[C@H](COC(=O)CC(O)=O)[C@@H](O)[C@H](O)[C@H]2O)=C3)C(O)=O)=C1)C(O)=O

InChIKey

InChIKey=PLRLSVAQXGDVOS-FGFIORFQSA-N

Formula

C27H28N2O16

Mass

636.519

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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 - Tetracarboxylic acid or derivatives - Indolecarboxylic acid derivative - Indolecarboxylic acid - O-glycosyl compound - Alpha-amino acid or derivatives - Alpha-amino acid - Pyridine carboxylic acid or derivatives - Pyridine carboxylic acid - Indole or derivatives - Tertiary aliphatic/aromatic amine - 1-hydroxy-2-unsubstituted benzenoid - Aralkylamine - Benzenoid - 1,3-dicarbonyl compound - Pyridine - Oxane - Monosaccharide - Heteroaromatic compound - Amino acid - Tertiary amine - Secondary alcohol - Carboxylic acid ester - Amino acid or derivatives - Oxacycle - Azacycle - Organoheterocyclic compound - Polyol - Enamine - Carboxylic acid - Carboxylic acid derivative - Acetal - Organic nitrogen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Aromatic alcohol - Organonitrogen compound - Carbonyl group - Amine - 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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