Metabolomics Structure Database

MDLMOL SDF CSV TSV

MW REGNO:	51829
Common Name:	1-linoleoyl-sn-glycero-3-phosphocholine
Systematic Name:	(2R)-2-hydroxy-3-[(9Z,12Z)-nonadeca-9,12-dienoyloxy]propyl 2-(trimethylammonio)ethyl phosphate
RefMet Name:	1-Linoleoyl-sn-glycero-3-phosphocholine
Synonyms:	1-(9Z,12Z-octadecadienoyl)-glycero-3-phosphocholine; 1-(9Z,12Z-octadecadienoyl)-sn-glycero-3-phosphocholine; 1-18:2-lysoPC; 1-linoleoyl-glycero-3-phosphocholine; LPC(18:2); LPC(18:2/0:0); LPC(18:2n6/0:0); LPC(18:2omega6/0:0); LyPC(18:2); LyPC(18:2n6/0:0); LyPC(18:2omega6/0:0); LysoPC(18:2); LysoPC(18:2/0:0); LysoPC(18:2n6/0:0); LysoPC(18:2omega6/0:0); Lysophosphatidylcholine(18:2); Lysophosphatidylcholine(18:2/0:0); Lysophosphatidylcholine(18:2n6/0:0); Lysophosphatidylcholine(18:2omega6/0:0) [PubChem Synonyms]
Exact Mass:	533.3481 (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:	C27H52NO7P
InChIKey:	FKSLBYVOWOXWMB-YTBCMDLOSA-N
LIPID MAPS Category:	Glycerophospholipids [GP]
LIPID MAPS mainclass:	Glycerophosphocholines [GP01]
LIPID MAPS subclass:	Monoacylglycerophosphocholines [GP0105]
SMILES:	CCCCCC/C=C\C/C=C\CCCCCCCC(=O)OC[C@H](COP(=O)([O-])OCC[N+](C)(C)C)O
Studies:	Available studies (via RefMet name)

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All Database Links Calculated Properties Human Pathways

External database links:

PubChem CID:	56955896
LIPID MAPS ID:	LMGP01050035
CHEBI ID:	28733

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