LBGPEccp:14000SC01:18000SC01:YS2ANe005

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IDs and Links
LipidBank	PGP2412
LipidMaps	[1]
CAS
KEGG	{{{KEGG}}}
KNApSAcK	{{{KNApSAcK}}}
mol	LBGPEccp:14000SC01:18000SC01:YS2ANe005

dimyristoyl-phosphatidylethanolamine
Structural Information
Systematic Name	1,2-di-myristoyl-sn-glycero- (3) -phosphoethanolamine
Common Name	dimyristoyl-phosphatidylethanolamine ethanolaminephosphoglyceride 1,2-dimyristoyl- (3-sn-phosphatidyl) ethanolamine dimyristoyl-L-a-phosphatidylethanolamine 1,2-di-myristoyl-sn-glycero- (3) -phosphoethanolamine
Symbol
Formula
Exact Mass
Average Mass
SMILES
Physicochemical Information
Melting Point	175-177°C <<2481/2482>>
Boiling Point
Density
Optical Rotation
Refractive Index
Solubility	Insoluble in water. At 20°C, synthetic PEs are insoluble (<=1mg/100 ml of dry solvent) in acetone, ether, petroleum ether, and ethyl acetate; moderately soluble (80 mg/100 ml of dry solvent) in EtOH, pyridine, benzene, and CCl4; readily soluble (> 1g/100 ml of solvent) in CHCl3. <<2482>>
Source
Chemical Synthesis
Metabolism
Biological Activity
Genetic Information
Note
Spectral Information
Mass Spectra
UV Spectra
IR Spectra	Fourier transform IR spectra for dimyristoyl-PE in the dry state (anhydrous), either in the pure state (A, C and E) or in the presence of 20 mol% of a-tocopherol (B, D and F). Ester C=O stretching vibration mode region,1800-1700 cm-1; CH2 deformation, scissoring band region, 1500-1400 cm-1; headgroup PO2- phosphate band region, 1350-1150 cm-1 File:LBGPEccp:14000SC01:18000SC01:YS2ANe005:01SP0001.gif <<2483>>.
NMR Spectra
Other Spectra
Chromatograms

Reported Metabolites, References

Biospecies ID Compound Name Reference Comment n.a. LBGPEccp:14000SC01:18000SC01:YS2ANe005 See above. Baer_E et al. 1952 n.a. LBGPEccp:14000SC01:18000SC01:YS2ANe005 See above. Blough_HA et al. 1973 n.a. LBGPEccp:14000SC01:18000SC01:YS2ANe005 See above. Kates_M 1964 n.a. LBGPEccp:14000SC01:18000SC01:YS2ANe005 See above. Kates_M 1970 n.a. LBGPEccp:14000SC01:18000SC01:YS2ANe005 See above. Salgado_J et al. 1995