Structure database (LMSD)
|Synonyms||Tetradecanoic acid, 2-hydroxy-3-(phosphonooxy)propyl ester, (R)-; 1-Myristoyl-|
sn-glycero-3-phosphate; 1-Myristoyl-sn-glycerol 3-phosphate
|Main Class||Glycerophosphates [GP10]|
|Sub Class||Monoacylglycerophosphates [GP1005]|
|PubChem Compound ID (CID)||9547180|
|InChIKey||FAZBDRGXCKPVJU-MRXNPFEDSA-N Show lipids differing only in stereochemistry/bond geometry|
|MS Standard||View lipid standard|
LIPID MAPS abbreviations for glycerophospholipids (GP)
The LIPID MAPS glycerophospholipid abbreviations (PC, PE, etc.) are used here to refer to species with one or two radyl side-chains where the structures of the side chains are indicated within parentheses in the 'Headgroup(sn1/sn2)' format (e.g. PC(16:0/18:1(9Z)). By default, R stereochemistry at the C-2 carbon of glycerol and attachment of the headgroup at the sn3 position is assumed. Also, acyl chains are assumed by default. The 'O-' prefix is used to indicate the presence of an alkyl ether substituent e.g. PC(O-16:0/18:1(9Z)), whereas the 'P-' prefix is used for the 1Z-alkenyl ether (Plasmalogen) substituent e.g. PC(P-16:0/18:1(9Z)).
For molecules with opposite (S) stereochemistry at C2 of the glycerol group and attachment of the headgroup at the sn1 position, the stereochemistry specification of [S] is appended to the abbreviation. The 'Headgroup(sn3/sn2)' abbreviation format is used.
For molecules with unknown stereochemistry at the C-2 carbon of the glycerol group, the stereochemistry specification of [U] is appended to the abbreviation and the structure is drawn with C-2 stereochemistry unspecified.