Structure Information
Structure

Compound Identification

SMILES

[Na+].CCCCCCCCCCCCCCCCCCOC[C@H](COP([O-])(=O)OC[C@@H](O)CO)OC(=O)CCCCCOC(=O)\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C

InChIKey

InChIKey=WGSLIDUYVUBRPN-DYWODMRVSA-M

Formula

C50H86NaO11P

Mass

917.191

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Lipids and lipid-like molecules

Class

Prenol lipids

Subclass

Retinoids

Intermediate Tree Nodes

Not available

Direct Parent

Retinoid esters

Alternative Parents

Molecular Framework

Aliphatic homomonocyclic compounds

Substituents

Retinoid ester - Diterpenoid - 1-alkyl,2-acylglycerophosphoglycerol - Glycero-3-phospho-1p-glycerol - Glycerophospholipid - Fatty acid ester - Dialkyl phosphate - Glycerol ether - Organic phosphoric acid derivative - Fatty acyl - Phosphoric acid ester - Dicarboxylic acid or derivatives - Alkyl phosphate - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Carboxylic acid ester - 1,2-diol - Secondary alcohol - Dialkyl ether - Ether - Organic alkali metal salt - Carboxylic acid derivative - Organic oxide - Alcohol - Organooxygen compound - Primary alcohol - Organic oxygen compound - Organic salt - Organic sodium salt - Hydrocarbon derivative - Carbonyl group - Organic cation - Aliphatic homomonocyclic compound

Description

This compound belongs to the class of organic compounds known as retinoid esters. These are ester derivatives of retinoic acid. These are obtained by formal condensation of the hydroxy group of retinol with the carboxy group of any carboxylic acid.

External Descriptors

Not available

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