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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2008-09-12 01:27:25 UTC
Update Date2022-11-30 19:03:05 UTC
HMDB IDHMDB0007866
Secondary Accession Numbers
  • HMDB07866
Metabolite Identification
Common NamePC(14:0/14:0)
DescriptionPC(14:0/14:0) is a phosphatidylcholine (PC or GPCho). It is a glycerophospholipid in which a phosphorylcholine moiety occupies a glycerol substitution site. As is the case with diacylglycerols, glycerophosphocholines can have many different combinations of fatty acids of varying lengths and saturation attached at the C-1 and C-2 positions. Fatty acids containing 16, 18 and 20 carbons are the most common. PC(14:0/14:0), in particular, consists of two chains of myristic acid at the C-1 and C-2 positions. The myristic acid moieties are derived from nutmeg and butter. Phospholipids, are ubiquitous in nature and are key components of the lipid bilayer of cells, as well as being involved in metabolism and signaling.While most phospholipids have a saturated fatty acid on C-1 and an unsaturated fatty acid on C-2 of the glycerol backbone, the fatty acid distribution at the C-1 and C-2 positions of glycerol within phospholipids is continually in flux, owing to phospholipid degradation and the continuous phospholipid remodeling that occurs while these molecules are in membranes. PCs can be synthesized via three different routes. In one route, choline is activated first by phosphorylation and then by coupling to CDP prior to attachment to phosphatidic acid. PCs can also synthesized by the addition of choline to CDP-activated 1,2-diacylglycerol. A third route to PC synthesis involves the conversion of either PS or PE to PC.
Structure
Data?1582752508
Synonyms
ValueSource
1,2-Di-O-tetradecanoyl-sn-glycero-3-phosphocholineChEBI
1,2-Dimyristoyl-GPCChEBI
1,2-Dimyristoyl-L-3-phosphatidylcholineChEBI
1,2-Dimyristoyl-sn-glycero-3-phosphocholineChEBI
1,2-DimyristoylphosphatidylcholineChEBI
1,2-Ditetradecanoyl-sn-glycero-3-phosphocholineChEBI
Dimyristoyl lecithinChEBI
Dimyristoyl phosphatidylcholineChEBI
DimyristoylphosphatidylcholineChEBI
DMPCChEBI
GPC(14:0/14:0)ChEBI
GPC(28:0)ChEBI
PC(28:0)ChEBI
Phosphatidylcholine(14:0/14:0)ChEBI
Phosphatidylcholine(28:0)ChEBI
1,2 Ditetradecanoyl glycero 3 phosphocholineHMDB
1,2-Ditetradecanoyl-glycero-3-phosphocholineHMDB
1,2-Ditetradecyl-glycero-3-phosphocholineHMDB
DMCPHMDB
DimyristoyllecithinHMDB
1,2 Dimyristoyl glycero 3 phosphorylcholineHMDB
1,2 Ditetradecyl glycero 3 phosphocholineHMDB
1,2-Dimyristoyl-glycero-3-phosphorylcholineHMDB
LecithinHMDB
1,2-Dimyristoyl-rac-glycero-3-phosphocholineHMDB
GPCho(28:0)HMDB
GPCho(14:0/14:0)HMDB
1,2-Ditetradecanoyl-rac-glycero-3-phosphocholineHMDB
PC(14:0/14:0)Lipid Annotator, ChEBI
Chemical FormulaC36H72NO8P
Average Molecular Weight677.9325
Monoisotopic Molecular Weight677.499554797
IUPAC Name(2-{[(2R)-2,3-bis(tetradecanoyloxy)propyl phosphono]oxy}ethyl)trimethylazanium
Traditional Name(2-{[(2R)-2,3-bis(tetradecanoyloxy)propyl phosphono]oxy}ethyl)trimethylazanium
CAS Registry Number18194-24-6
SMILES
[H][C@@](COC(=O)CCCCCCCCCCCCC)(COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCCCCCCCC
InChI Identifier
InChI=1S/C36H72NO8P/c1-6-8-10-12-14-16-18-20-22-24-26-28-35(38)42-32-34(33-44-46(40,41)43-31-30-37(3,4)5)45-36(39)29-27-25-23-21-19-17-15-13-11-9-7-2/h34H,6-33H2,1-5H3/t34-/m1/s1
InChI KeyCITHEXJVPOWHKC-UUWRZZSWSA-N
Chemical Taxonomy
Description 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.
KingdomOrganic compounds
Super ClassLipids and lipid-like molecules
ClassGlycerophospholipids
Sub ClassGlycerophosphocholines
Direct ParentPhosphatidylcholines
Alternative Parents
Substituents
  • Diacylglycero-3-phosphocholine
  • Phosphocholine
  • Fatty acid ester
  • Dialkyl phosphate
  • Dicarboxylic acid or derivatives
  • Organic phosphoric acid derivative
  • Phosphoric acid ester
  • Alkyl phosphate
  • Fatty acyl
  • Quaternary ammonium salt
  • Tetraalkylammonium salt
  • Carboxylic acid ester
  • Carboxylic acid derivative
  • Organic oxygen compound
  • Organic nitrogen compound
  • Carbonyl group
  • Organooxygen compound
  • Organonitrogen compound
  • Organic oxide
  • Organopnictogen compound
  • Amine
  • Organic salt
  • Hydrocarbon derivative
  • Aliphatic acyclic compound
Molecular FrameworkAliphatic acyclic compounds
External Descriptors
Ontology
Physiological effect
Disposition
Biological locationRoute of exposureSource
Process
Naturally occurring process