Structure Information
Structure

Compound Identification

SMILES

CCCCCCCCCCCCCCCC(=O)O[C@H](COC(=O)CCCCCNC(=O)CCCCCNC1=CC=C(C2=NON=C12)[N+]([O-])=O)COP(O)(=O)OCC

InChIKey

InChIKey=QGFKGFRLRJQCQZ-JGCGQSQUSA-N

Formula

C39H66N5O12P

Mass

827.954

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Lipids and lipid-like molecules

Class

Glycerophospholipids

Subclass

Phosphatidylethanols

Intermediate Tree Nodes

Not available

Direct Parent

Phosphatidylethanols

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Phosphatidylethanol - Benzoxadiazole - Nitroaromatic compound - Secondary aliphatic/aromatic amine - Dialkyl phosphate - Fatty acid ester - Phosphoric acid ester - Alkyl phosphate - Organic phosphoric acid derivative - Benzenoid - N-acyl-amine - Fatty amide - Fatty acyl - Dicarboxylic acid or derivatives - Azole - Furazan - Heteroaromatic compound - Oxadiazole - C-nitro compound - Secondary carboxylic acid amide - Amino acid or derivatives - Carboxamide group - Organic nitro compound - Carboxylic acid ester - Carboxylic acid derivative - Oxacycle - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic oxoazanium - Secondary amine - Organic oxygen compound - Organic salt - Organic oxide - Carbonyl group - Hydrocarbon derivative - Amine - Organic zwitterion - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as phosphatidylethanols. These are glycerophospholipids where the central glycerol is acylated at the 1- and 2-positions by two acyl chains, and is linked at the 3-position to a phosphoethanol. They are phospholipids formed only in the presence of ethanol via the action of phospholipase D.

External Descriptors

Not available

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