Metabolomics Structure Database

MDLMOL SDF CSV TSV

MW REGNO:	13693
Common Name:	PC(6:0/6:0)
Systematic Name:	1,2-dihexanoyl-sn-glycero-3-phosphocholine
Synonyms:	3,5,9-Trioxa-4-phosphapentadecan-1-aminium, 4-hydroxy-N,N,N-trimethyl-10-oxo-7-[(1-oxohexyl)oxy]-, inner salt, 4-oxide, (R)-; Choline, hydroxide, dihydrogen phosphate, inner salt, ester with 1,2-dihexanoin, L-; 1,2-Dihexanoyl-L-alpha-glycerophosphorylcholine; 1,2-Dihexanoyl-sn-3-glycerophosphocholine; 1,2-Dihexanoyl-sn-glycerol-3-phosphocholine; Dicaproyl-L-alpha-lecithin; Dihexanoyllecithin; L-alpha-Dihexanoyllecithin; L-alpha-Dihexanoylphosphatidylcholine; L-1,2-Dihexanoyllecithin [PubChem Synonyms]
Exact Mass:	453.2492 (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:	C20H40NO8P
InChIKey:	DVZARZBAWHITHR-GOSISDBHSA-N
LIPID MAPS Category:	Glycerophospholipids [GP]
LIPID MAPS mainclass:	Glycerophosphocholines [GP01]
LIPID MAPS subclass:	Diacylglycerophosphocholines [GP0101]
SMILES:	CCCCCC(=O)OC[C@H](COP(=O)([O-])OCC[N+](C)(C)C)OC(=O)CCCCC
Studies:	-

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External database links:

PubChem CID:	10072611
LIPID MAPS ID:	LMGP01011229
CHEBI ID:	138194

Calculated physicochemical properties (?):

Heavy Atoms:	30
Rings:	0
Aromatic Rings:	0
Rotatable Bonds:	20
van der Waals Molecular volume:	450.43 Å3 molecule-1
Toplogical Polar Sufrace Area:	111.19 Å2 molecule-1
Hydrogen Bond Donors:	0
Hydrogen Bond Acceptors:	9
logP:	4.24
Molar Refractivity:	114.00
Fraction sp3 Carbons:	0.90
sp3 Carbons:	18

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