Metabolomics Structure Database

MDLMOL SDF CSV TSV

MW REGNO:	13463
Common Name:	PC(18:0/14:0)
Systematic Name:	1-octadecanoyl-2-tetradecanoyl-sn-glycero-3-phosphocholine
RefMet Name:	PC 18:0/14:0
Synonyms:	3,5,9-Trioxa-4-phosphaheptacosan-1-aminium, 4-hydroxy-N,N,N-trimethyl-10-oxo-7-[(1-oxotetradecyl)oxy]-, inner salt, 4-oxide, (R)-; Choline, hydroxide, dihydrogen phosphate, inner salt, ester with 2-myristo-1-stearin, L-; Myristin, 1-stearo-2-, dihydrogen phosphate, monoester with choline hydroxide, inner salt, L-; Stearin, 2-myristo-1-, dihydrogen phosphate, monoester with choline hydroxide, inner salt, (R)-; 1-Stearoyl-2-myristoyl-sn-glycero-3-phosphoryl choline; 1-Stearoyl-2-myristoylphosphatidylcholine [PubChem Synonyms]
Exact Mass:	733.5622 (neutral)    Calculate m/z: (Choose adduct) [M+H]+ [M+H-H2O]+ [M.]+ [M+2H]2+ [M+3H]3+ [M+4H]4+ [M+K]+ [M+2K]2+ [M-H+2K]+ [M+Na]+ [M+2Na]2+ [M-H+2Na]+ [M+Li]+ [M+2Li]2+ [M+NH4]+ [M-H]- [M-2H]2- [M-3H]3- [M-4H]4- [M+Cl]- [M+OAc]- [M+HCOO]- M(neutral)
Formula:	C40H80NO8P
InChIKey:	MZWGYEJOZNRLQE-KXQOOQHDSA-N
LIPID MAPS Category:	Glycerophospholipids [GP]
LIPID MAPS mainclass:	Glycerophosphocholines [GP01]
LIPID MAPS subclass:	Diacylglycerophosphocholines [GP0101]
SMILES:	CCCCCCCCCCCCCCCCCC(=O)OC[C@H](COP(=O)([O-])OCC[N+](C)(C)C)OC(=O)CCCCCCCCCCCCC
Studies:	Available studies (via RefMet name)

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All Database Links Calculated Properties Human Pathways

External database links:

PubChem CID:	3082163
LIPID MAPS ID:	LMGP01010739
CHEBI ID:	86089
HMDB ID:	HMDB0008031
Chemspider ID:	2339631

References

LIPID MAPS classification: "Update of the LIPID MAPS comprehensive classification system for lipids", Fahy E, Subramaniam S, Murphy RC, Nishijima M, Raetz CR, Shimizu T, Spener F, van Meer G, Wakelam MJ, and Dennis EA, J. Lipid Res. (2009) 50: S9-S14. DOI: 10.1194/jlr.R800095-JLR200
ClassyFire classification: "ClassyFire: automated chemical classification with a comprehensive, computable taxonomy", Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS, J. Cheminformatics (2016) 8:61. DOI: 10.1186/s13321-016-0174-y