Structure Information
Structure

Compound Identification

SMILES

CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCCCCCN(C)C1=CC=C(C2=NON=C12)[N+]([O-])=O

InChIKey

InChIKey=ORIATWTXJGGODP-PSXMRANNSA-N

Formula

C42H74N5O11P

Mass

856.052

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Lipids and lipid-like molecules

Class

Glycerophospholipids

Subclass

Glycerophosphocholines

Intermediate Tree Nodes

Not available

Direct Parent

Phosphatidylcholines

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Diacylglycero-3-phosphocholine - Phosphocholine - Nitroaromatic compound - Dialkylarylamine - Tertiary aliphatic/aromatic amine - Fatty acid ester - Fatty acyl - Benzenoid - Alkyl phosphate - Phosphoric acid ester - Organic phosphoric acid derivative - Dicarboxylic acid or derivatives - Tetraalkylammonium salt - Heteroaromatic compound - Quaternary ammonium salt - Oxadiazole - Furazan - Azole - Organic nitro compound - Tertiary aliphatic amine - Tertiary amine - C-nitro compound - Carboxylic acid ester - Amino acid or derivatives - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic oxoazanium - Enamine - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organic salt - Organooxygen compound - Organonitrogen compound - Organic hyponitrite - Amine - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as phosphatidylcholines. These are glycerophosphocholines in which the two free -OH are attached to one fatty acid each through an ester linkage.

External Descriptors

Not available

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