Structure Information
Structure

Compound Identification

SMILES

COC(=O)C1OC(OC2=CC=C(NC(C)=O)C=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C

InChIKey

InChIKey=UGPNIYXOVJVQGC-UHFFFAOYSA-N

Formula

C24H43NO8Si3

Mass

557.862

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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 - O-glucuronide - 1-o-glucuronide - Glucuronic acid or derivatives - O-glycosyl compound - Acetanilide - N-acetylarylamine - Anilide - Phenol ether - N-arylamide - Phenoxy compound - Monocyclic benzene moiety - Benzenoid - Pyran - Oxane - Monosaccharide - Trialkylheterosilane - Acetamide - Methyl ester - Secondary carboxylic acid amide - Silyl ether - Carboxamide group - Carboxylic acid ester - Acetal - Organoheterosilane - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Oxacycle - Organic metalloid salt - Organoheterocyclic compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Carbonyl group - Organic nitrogen compound - Organic salt - Organonitrogen compound - Organosilicon 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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