Metabolomics Structure Database

MDLMOL SDF CSV TSV

MW REGNO:	20029
Common Name:	PA(16:0/16:0)
Systematic Name:	1,2-dihexadecanoyl-sn-glycero-3-phosphate
RefMet Name:	PA 16:0/16:0
Synonyms:	Dipalmitoyl phosphatidic acid; Hexadecanoic acid, 1-[(phosphonooxy)methyl]-1,2-ethanediyl ester, (R)-; Palmitin, 1,2-di-, dihydrogen phosphate, L-; 1,2-Dipalmitoyl-3-sn-phosphatidic acid; 1,2-Dipalmitoyl-sn-glycerol 3-phosphate; 1,2-Dipalmitoyl-sn-glycerol-3-phosphoric acid; Dipalmitoyl [PubChem Synonyms]
Exact Mass:	648.4730 (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:	C35H69O8P
InChIKey:	PORPENFLTBBHSG-MGBGTMOVSA-N
LIPID MAPS Category:	Glycerophospholipids [GP]
LIPID MAPS mainclass:	Glycerophosphates [GP10]
LIPID MAPS subclass:	Diacylglycerophosphates [GP1001]
NP-MRD NMR spectra:	View NMR spectra
SMILES:	CCCCCCCCCCCCCCCC(=O)OC[C@H](COP(=O)(O)O)OC(=O)CCCCCCCCCCCCCCC
Studies:	Available studies (via RefMet name)

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All Database Links Calculated Properties Human Pathways

Calculated physicochemical properties (?):

Heavy Atoms:	44
Rings:	0
Aromatic Rings:	0
Rotatable Bonds:	36
van der Waals Molecular volume:	698.93 Å3 molecule-1
Toplogical Polar Sufrace Area:	119.36 Å2 molecule-1
Hydrogen Bond Donors:	2
Hydrogen Bond Acceptors:	8
logP:	11.71
Molar Refractivity:	180.68
Fraction sp3 Carbons:	0.94
sp3 Carbons:	33

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