Structure Information
Structure

Compound Identification

SMILES

CSC(CC1=CC=C(OCC2=NC3=C(C=C(O[C@@H]4O[C@@H](C(O)[C@H](O)[C@H]4O)C(O)=O)C=C3)N2C)C=C1)C(N)=O

InChIKey

InChIKey=XIJFKAARBURGKF-GLVYVHRTSA-N

Formula

C25H29N3O9S

Mass

547.58

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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 - 1-o-glucuronide - O-glucuronide - Glucuronic acid or derivatives - Hexose monosaccharide - O-glycosyl compound - Benzimidazole - Phenoxy compound - Phenol ether - Alkyl aryl ether - Beta-hydroxy acid - Monocyclic benzene moiety - Fatty amide - Hydroxy acid - Monosaccharide - N-substituted imidazole - Fatty acyl - Oxane - Pyran - Benzenoid - Heteroaromatic compound - Imidazole - Azole - Carboxamide group - Primary carboxylic acid amide - Secondary alcohol - Oxacycle - Azacycle - Monocarboxylic acid or derivatives - Acetal - Thioether - Sulfenyl compound - Polyol - Organoheterocyclic compound - Ether - Carboxylic acid - Carboxylic acid derivative - Dialkylthioether - Organopnictogen compound - Alcohol - Hydrocarbon derivative - Organic nitrogen compound - Organic oxide - Organonitrogen compound - Organosulfur compound - Carbonyl group - 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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