Structure Information
Structure

Compound Identification

SMILES

C\C(CO)=C1/C[C@H]2[C@H]3C[C@H]4C[C@]56C=CC[C@]78Oc9ccc%10C(CO)=C([C@H](CCO)COCO)C(=O)Oc%10c9[C@@H](OC(=O)C[C@@H]9C[C@H](C=C[C@@H]9c9ccc2c4c9)c2cccc4c2CC[C@@H]2CCC[C@@H]9C=Cc%10ccc(Cc%11ccc(cc%11)[C@@]33CCC[C@H]3C#CC3=Cc%11ccccc%11[C@@H](C[C@@H]57)[C@@H]63)cc%10[C@]429)[C@@H]8OC1=O

InChIKey

InChIKey=FJQSKUUEVYAHNY-VTDYFKSESA-N

Formula

C95H92O12

Mass

1425.769

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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

Aromatic heteropolycyclic compounds

Substituents

Retinoid ester - Diterpenoid - Diterpene lactone - Lignan lactone - Norlignan skeleton - C8-prenylated coumarin - Angular pyranocoumarin - Pyranocoumarin - Pyranochromene - Phenanthrene - Fatty alcohol ester - Coumarin - 1-benzopyran - Tetralin - Naphthalene - Benzopyran - Chromane - Fatty alcohol - Pyranone - Fatty acid ester - Alkyl aryl ether - Fatty acyl - Benzenoid - Pyran - Dicarboxylic acid or derivatives - Heteroaromatic compound - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Lactone - Hemiacetal - Carboxylic acid ester - Haloacetylene or derivatives - Oxacycle - Organoheterocyclic compound - Ether - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Aromatic alcohol - Organooxygen compound - Alcohol - Aromatic heteropolycyclic 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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