LBGPEc-p:R::YS2ANe005: Difference between revisions

 
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|LipidBank=PGP2416
|LipidBank=PGP2416
|SysName=1-acyl-sn-glycero- (3) -phosphoethanolamine
|SysName=1-acyl-sn-glycero- (3) -phosphoethanolamine
|Common Name=&&lysophosphatidylethanolamine&&1-acyl &&1-acyl-sn-glycero- (3) -phosphoethanolamine&&
|Common Name=&&lysophosphatidylethanolamine&&1-acyl&&
|Melting Point=205° <<2520>>; 1-palmitoyl-DL-lysoPE, 212°C <<2517>>
|Melting Point=205° <<2520>>; 1-palmitoyl-DL-lysoPE, 212°C <<2517>>
|Chromatograms=Two-dimensional thin-layer chromatography. Silica gel 60 plate (Merch, Germany) was done in the first developement solution, composed of tetrahydrofuran-acetone-methanol-water (50: 20: 40: 8, by volume), and in the second developement solution, composed of chloroform-acetone-methanol-acetic acid-water (50: 20: 10: 15: 5, by volume) {{Image200|LBGPEc-p:R::YS2ANe005:01CH0001.gif}} <<2521>>./<BR>HPLC: PE,dipalmitoyl-phosphatidylethanolamine; LPE,1-palmitoyl-glycerophosphorylethanolamine; PC,dipalmitoyl-phosphatidylcholine; LPC,1-palmitoyl-glycerophosphorylcholine {{Image200|LBGPEc-p:R::YS2ANe005:01CH0002.gif}} <<2522>>.,  
|Chromatograms=Two-dimensional thin-layer chromatography. Silica gel 60 plate (Merch, Germany) was done in the first developement solution, composed of tetrahydrofuran-acetone-methanol-water (50: 20: 40: 8, by volume), and in the second developement solution, composed of chloroform-acetone-methanol-acetic acid-water (50: 20: 10: 15: 5, by volume) {{Image200|LBGPEc-p:R::YS2ANe005CH0001.gif}} <<2521>>./<BR>HPLC: PE,dipalmitoyl-phosphatidylethanolamine; LPE,1-palmitoyl-glycerophosphorylethanolamine; PC,dipalmitoyl-phosphatidylcholine; LPC,1-palmitoyl-glycerophosphorylcholine {{Image200|LBGPEc-p:R::YS2ANe005CH0002.gif}} <<2522>>.,  
}}
}}


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{{Lipid/Footer}}

Latest revision as of 21:00, 14 April 2010

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lysophosphatidylethanolamine
LBGPEc-p:R::YS2ANe005.png
Structural Information
1-acyl-sn-glycero- (3) -phosphoethanolamine
  • lysophosphatidylethanolamine
  • 1-acyl
Formula
Exact Mass
Average Mass
SMILES
Physicochemical Information
205° <<2520>>; 1-palmitoyl-DL-lysoPE, 212°C <<2517>>
Spectral Information
Mass Spectra
UV Spectra
IR Spectra
NMR Spectra
Other Spectra
Chromatograms Two-dimensional thin-layer chromatography. Silica gel 60 plate (Merch, Germany) was done in the first developement solution, composed of tetrahydrofuran-acetone-methanol-water (50: 20: 40: 8, by volume), and in the second developement solution, composed of chloroform-acetone-methanol-acetic acid-water (50: 20: 10: 15: 5, by volume)
LBGPEc-p:R::YS2ANe005CH0001.gif
<<2521>>./
HPLC: PE,dipalmitoyl-phosphatidylethanolamine; LPE,1-palmitoyl-glycerophosphorylethanolamine; PC,dipalmitoyl-phosphatidylcholine; LPC,1-palmitoyl-glycerophosphorylcholine
LBGPEc-p:R::YS2ANe005CH0002.gif
<<2522>>.,
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBGPEc-p:R::YS2ANe005 See above. Billimoria_JD et al. 1968
n.a. LBGPEc-p:R::YS2ANe005 See above. Chattopadhyay_P et al. 1985
n.a. LBGPEc-p:R::YS2ANe005 See above. Dunkley_EA_Jr et al. 1988
n.a. LBGPEc-p:R::YS2ANe005:01 Gruner_SM et al. 1988
n.a. LBGPEc-p:R::YS2ANe005 See above. Holt_SC et al. 1979
n.a. LBGPEc-p:R::YS2ANe005 See above. Ikeda_Y et al. 1997
n.a. LBGPEc-p:R::YS2ANe005 See above. Lee_FC et al. 1980
n.a. LBGPEc-p:R::YS2ANe005 See above. Martiny-Baron_G et al. 1989
n.a. LBGPEc-p:R::YS2ANe005 See above. Pugsley_AP et al. 1985
n.a. LBGPEc-p:R::YS2ANe005 See above. Rosenthal_AF 1975
n.a. LBGPEc-p:R::YS2ANe005 See above. Ryu_SB et al. 1997
n.a. LBGPEc-p:R::YS2ANe005 See above. Senff_LM et al. 1976
n.a. LBGPEc-p:R::YS2ANe005 See above. Slotboom_AJ et al. 1970
n.a. LBGPEc-p:R::YS2ANe005 See above. Thumser_AE et al. 1994