LBGPEccp:R:R:p - Revision history

Editor: LBGPEccp:R:R:ppppppppp:01 moved to LBGPEccp:R:R:p

2010-04-14T21:00:00Z

LBGPEccp:R:R:ppppppppp:01 moved to LBGPEccp:R:R:p

← Older revision		Revision as of 06:00, 15 April 2010
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	\|LipidBank=PGP2404		\|LipidBank=PGP2404
	\|SysName=1,2-di-acyl-sn-glycero- (3) -phospho-N,N-dimethylethanolamine		\|SysName=1,2-di-acyl-sn-glycero- (3) -phospho-N,N-dimethylethanolamine
	\|Common Name=&&phosphatidyl-N,N-dimethylethanolamine&&N,N-dimethylphosphatidylethanolamine ~~&&1,2-di-acyl-sn-glycero- (3) -phospho-N,N-dimethylethanolamine~~&&		\|Common Name=&&phosphatidyl-N,N-dimethylethanolamine&&N,N-dimethylphosphatidylethanolamine&&
	\|Melting Point=1,2-distearoyl-L-N,N-dimethylphosphatidylethanolamine, 168-169°C; 1,2-distearoyl-DL-N,N-dimethylphosphatidylethanolamine, 160-162°C; 1,2-dipalmitoyl-L-N,N-dimethylphosphatidylethanolamine, 164-165°C; 1,2-dipalmitoyl-DL-N,N-dimethylphosphatidylethanolamine, 160-161°C <<2437>>		\|Melting Point=1,2-distearoyl-L-N,N-dimethylphosphatidylethanolamine, 168-169°C; 1,2-distearoyl-DL-N,N-dimethylphosphatidylethanolamine, 160-162°C; 1,2-dipalmitoyl-L-N,N-dimethylphosphatidylethanolamine, 164-165°C; 1,2-dipalmitoyl-DL-N,N-dimethylphosphatidylethanolamine, 160-161°C <<2437>>
	\|Reflactive=1,2-distearoyl-L-N-methylphosphatidylethanolamine, [ alpha ]^{25}_D +5.8°; 1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, [ alpha ]^{25}_D +5.8° <<2437>>		\|Reflactive=1,2-distearoyl-L-N-methylphosphatidylethanolamine, [ alpha ]^{25}_D +5.8°; 1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, [ alpha ]^{25}_D +5.8° <<2437>>

Editor: LBGPEccp:R:R:ppppppppp:01 moved to LBGPEccp:R:R:p

2010-02-25T10:00:10Z

LBGPEccp:R:R:ppppppppp:01 moved to LBGPEccp:R:R:p

← Older revision		Revision as of 19:00, 25 February 2010
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	\|Common Name=&&phosphatidyl-N,N-dimethylethanolamine&&N,N-dimethylphosphatidylethanolamine &&1,2-di-acyl-sn-glycero- (3) -phospho-N,N-dimethylethanolamine&&		\|Common Name=&&phosphatidyl-N,N-dimethylethanolamine&&N,N-dimethylphosphatidylethanolamine &&1,2-di-acyl-sn-glycero- (3) -phospho-N,N-dimethylethanolamine&&
	\|Melting Point=1,2-distearoyl-L-N,N-dimethylphosphatidylethanolamine, 168-169°C; 1,2-distearoyl-DL-N,N-dimethylphosphatidylethanolamine, 160-162°C; 1,2-dipalmitoyl-L-N,N-dimethylphosphatidylethanolamine, 164-165°C; 1,2-dipalmitoyl-DL-N,N-dimethylphosphatidylethanolamine, 160-161°C <<2437>>		\|Melting Point=1,2-distearoyl-L-N,N-dimethylphosphatidylethanolamine, 168-169°C; 1,2-distearoyl-DL-N,N-dimethylphosphatidylethanolamine, 160-162°C; 1,2-dipalmitoyl-L-N,N-dimethylphosphatidylethanolamine, 164-165°C; 1,2-dipalmitoyl-DL-N,N-dimethylphosphatidylethanolamine, 160-161°C <<2437>>
	\|Reflactive=1,2-distearoyl-L-N-methylphosphatidylethanolamine, [ alpha ]^~~25_D~~ +5.8°; 1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, [ alpha ]^~~25_D~~ +5.8° <<2437>>		\|Reflactive=1,2-distearoyl-L-N-methylphosphatidylethanolamine, [ alpha ]^{25}_D +5.8°; 1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, [ alpha ]^{25}_D +5.8° <<2437>>
	\|NMR Spectra=^2 H-NMR spectra of PC, PDME, PMME, and PE fully hydrated with D_2 O at the indicated temperatures {{Image200\|LBGPEccp:R:R:pSP0001.gif}} <<2435>>.,		\|NMR Spectra=^2 H-NMR spectra of PC, PDME, PMME, and PE fully hydrated with D_2 O at the indicated temperatures {{Image200\|LBGPEccp:R:R:pSP0001.gif}} <<2435>>.,
	\|Chromatograms=HPLC, mu Bondapak NH_2 , acetonitril-methanol-water (13:7:1, v/v), elution rate 1.6 ml/min, detection ~~OD_2 _0 _3~~ nm, Peaks: SF = solvent front, PC = phosphatidylcholine, SPH = sphingomyelin, LPC = lysophosphatidylcholine, PMME = phosphatidylmonomethylethanolamine, PE = phosphatidylethanolamine, PDME = phosphatidyldimethylethanolamine, LPE = lysophosphatidylethanolamine, {{Image200\|LBGPEccp:R:R:pCH0001.gif}} <<2426>>/<BR>TLC, plate: Silica gel 60 (Merck, 20 X 20 cm, 0.25 mm thick), solvent: 1st dim. chloroform - methanol - water (65:25:4, v/v), 2nd dim. n-butanol - acetic acid - water (6:2:2, v/v) <<2427>>,		\|Chromatograms=HPLC, mu Bondapak NH_2 , acetonitril-methanol-water (13:7:1, v/v), elution rate 1.6 ml/min, detection OD_{203} nm, Peaks: SF = solvent front, PC = phosphatidylcholine, SPH = sphingomyelin, LPC = lysophosphatidylcholine, PMME = phosphatidylmonomethylethanolamine, PE = phosphatidylethanolamine, PDME = phosphatidyldimethylethanolamine, LPE = lysophosphatidylethanolamine, {{Image200\|LBGPEccp:R:R:pCH0001.gif}} <<2426>>/<BR>TLC, plate: Silica gel 60 (Merck, 20 X 20 cm, 0.25 mm thick), solvent: 1st dim. chloroform - methanol - water (65:25:4, v/v), 2nd dim. n-butanol - acetic acid - water (6:2:2, v/v) <<2427>>,
	}}		}}

	{{Lipid/Footer}}		{{Lipid/Footer}}

Editor: LBGPEccp:R:R:ppppppppp:01 moved to LBGPEccp:R:R:p

2010-02-19T14:00:10Z

LBGPEccp:R:R:ppppppppp:01 moved to LBGPEccp:R:R:p

← Older revision		Revision as of 23:00, 19 February 2010
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	\|Common Name=&&phosphatidyl-N,N-dimethylethanolamine&&N,N-dimethylphosphatidylethanolamine &&1,2-di-acyl-sn-glycero- (3) -phospho-N,N-dimethylethanolamine&&		\|Common Name=&&phosphatidyl-N,N-dimethylethanolamine&&N,N-dimethylphosphatidylethanolamine &&1,2-di-acyl-sn-glycero- (3) -phospho-N,N-dimethylethanolamine&&
	\|Melting Point=1,2-distearoyl-L-N,N-dimethylphosphatidylethanolamine, 168-169°C; 1,2-distearoyl-DL-N,N-dimethylphosphatidylethanolamine, 160-162°C; 1,2-dipalmitoyl-L-N,N-dimethylphosphatidylethanolamine, 164-165°C; 1,2-dipalmitoyl-DL-N,N-dimethylphosphatidylethanolamine, 160-161°C <<2437>>		\|Melting Point=1,2-distearoyl-L-N,N-dimethylphosphatidylethanolamine, 168-169°C; 1,2-distearoyl-DL-N,N-dimethylphosphatidylethanolamine, 160-162°C; 1,2-dipalmitoyl-L-N,N-dimethylphosphatidylethanolamine, 164-165°C; 1,2-dipalmitoyl-DL-N,N-dimethylphosphatidylethanolamine, 160-161°C <<2437>>
	\|Reflactive=1,2-distearoyl-L-N-methylphosphatidylethanolamine, [alpha]^25_D +5.8°; 1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, [alpha]^25_D +5.8° <<2437>>		\|Reflactive=1,2-distearoyl-L-N-methylphosphatidylethanolamine, [ alpha ]^25_D +5.8°; 1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, [ alpha ]^25_D +5.8° <<2437>>
	\|NMR Spectra=^2 H-NMR spectra of PC, PDME, PMME, and PE fully hydrated with D_2 O at the indicated temperatures {{Image200\|LBGPEccp:R:R:pSP0001.gif}} <<2435>>.,		\|NMR Spectra=^2 H-NMR spectra of PC, PDME, PMME, and PE fully hydrated with D_2 O at the indicated temperatures {{Image200\|LBGPEccp:R:R:pSP0001.gif}} <<2435>>.,
	\|Chromatograms=HPLC, ~~muBondapak~~ NH_2 , acetonitril-methanol-water (13:7:1, v/v), elution rate 1.6 ml/min, detection OD_2 _0 _3 nm, Peaks: SF = solvent front, PC = phosphatidylcholine, SPH = sphingomyelin, LPC = lysophosphatidylcholine, PMME = phosphatidylmonomethylethanolamine, PE = phosphatidylethanolamine, PDME = phosphatidyldimethylethanolamine, LPE = lysophosphatidylethanolamine, {{Image200\|LBGPEccp:R:R:pCH0001.gif}} <<2426>>/<BR>TLC, plate: Silica gel 60 (Merck, 20 X 20 cm, 0.25 mm thick), solvent: 1st dim. chloroform - methanol - water (65:25:4, v/v), 2nd dim. n-butanol - acetic acid - water (6:2:2, v/v) <<2427>>,		\|Chromatograms=HPLC, mu Bondapak NH_2 , acetonitril-methanol-water (13:7:1, v/v), elution rate 1.6 ml/min, detection OD_2 _0 _3 nm, Peaks: SF = solvent front, PC = phosphatidylcholine, SPH = sphingomyelin, LPC = lysophosphatidylcholine, PMME = phosphatidylmonomethylethanolamine, PE = phosphatidylethanolamine, PDME = phosphatidyldimethylethanolamine, LPE = lysophosphatidylethanolamine, {{Image200\|LBGPEccp:R:R:pCH0001.gif}} <<2426>>/<BR>TLC, plate: Silica gel 60 (Merck, 20 X 20 cm, 0.25 mm thick), solvent: 1st dim. chloroform - methanol - water (65:25:4, v/v), 2nd dim. n-butanol - acetic acid - water (6:2:2, v/v) <<2427>>,
	}}		}}

	{{Lipid/Footer}}		{{Lipid/Footer}}

Editor: LBGPEccp:R:R:ppppppppp:01 moved to LBGPEccp:R:R:p

2010-02-19T14:00:00Z

LBGPEccp:R:R:ppppppppp:01 moved to LBGPEccp:R:R:p

← Older revision		Revision as of 23:00, 19 February 2010
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	\|Common Name=&&phosphatidyl-N,N-dimethylethanolamine&&N,N-dimethylphosphatidylethanolamine &&1,2-di-acyl-sn-glycero- (3) -phospho-N,N-dimethylethanolamine&&		\|Common Name=&&phosphatidyl-N,N-dimethylethanolamine&&N,N-dimethylphosphatidylethanolamine &&1,2-di-acyl-sn-glycero- (3) -phospho-N,N-dimethylethanolamine&&
	\|Melting Point=1,2-distearoyl-L-N,N-dimethylphosphatidylethanolamine, 168-169°C; 1,2-distearoyl-DL-N,N-dimethylphosphatidylethanolamine, 160-162°C; 1,2-dipalmitoyl-L-N,N-dimethylphosphatidylethanolamine, 164-165°C; 1,2-dipalmitoyl-DL-N,N-dimethylphosphatidylethanolamine, 160-161°C <<2437>>		\|Melting Point=1,2-distearoyl-L-N,N-dimethylphosphatidylethanolamine, 168-169°C; 1,2-distearoyl-DL-N,N-dimethylphosphatidylethanolamine, 160-162°C; 1,2-dipalmitoyl-L-N,N-dimethylphosphatidylethanolamine, 164-165°C; 1,2-dipalmitoyl-DL-N,N-dimethylphosphatidylethanolamine, 160-161°C <<2437>>
	\|Reflactive=1,2-distearoyl-L-N-methylphosphatidylethanolamine, [~~<FONT FACE="Symbol">a</FONT>~~]~~<sub>D</sub><sup>25</sup>~~ +5.8°; 1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, [~~<FONT FACE="Symbol">a</FONT>~~]~~<sub>D</sub><sup>25</sup>~~ +5.8° <<2437>>		\|Reflactive=1,2-distearoyl-L-N-methylphosphatidylethanolamine, [alpha]^25_D +5.8°; 1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, [alpha]^25_D +5.8° <<2437>>
	\|NMR Spectra=~~<SUP><FONT SIZE=-1>~~2~~</FONT></SUP>~~H-NMR spectra of PC, PDME, PMME, and PE fully hydrated with ~~D<SUB><FONT SIZE=-1>2</FONT></SUB>~~O at the indicated temperatures {{Image200\|LBGPEccp:R:R:pSP0001.gif}} <<2435>>.,		\|NMR Spectra=^2 H-NMR spectra of PC, PDME, PMME, and PE fully hydrated with D_2 O at the indicated temperatures {{Image200\|LBGPEccp:R:R:pSP0001.gif}} <<2435>>.,
	\|Chromatograms=HPLC, ~~<FONT FACE="Symbol">m</FONT>Bondapak NH<SUB><FONT SIZE=-1>2</FONT></SUB>~~, acetonitril-methanol-water (13:7:1, v/v), elution rate 1.6 ml/min, detection ~~OD<SUB><FONT SIZE=-1>2</FONT></SUB><SUB><FONT SIZE=-1>0</FONT></SUB><SUB><FONT SIZE=-1>3</FONT></SUB>~~ nm, Peaks: SF = solvent front, PC = phosphatidylcholine, SPH = sphingomyelin, LPC = lysophosphatidylcholine, PMME = phosphatidylmonomethylethanolamine, PE = phosphatidylethanolamine, PDME = phosphatidyldimethylethanolamine, LPE = lysophosphatidylethanolamine, {{Image200\|LBGPEccp:R:R:pCH0001.gif}} <<2426>>/<BR>TLC, plate: Silica gel 60 (Merck, 20 X 20 cm, 0.25 mm thick), solvent: 1st dim. chloroform - methanol - water (65:25:4, v/v), 2nd dim. n-butanol - acetic acid - water (6:2:2, v/v) <<2427>>,		\|Chromatograms=HPLC, muBondapak NH_2 , acetonitril-methanol-water (13:7:1, v/v), elution rate 1.6 ml/min, detection OD_2 _0 _3 nm, Peaks: SF = solvent front, PC = phosphatidylcholine, SPH = sphingomyelin, LPC = lysophosphatidylcholine, PMME = phosphatidylmonomethylethanolamine, PE = phosphatidylethanolamine, PDME = phosphatidyldimethylethanolamine, LPE = lysophosphatidylethanolamine, {{Image200\|LBGPEccp:R:R:pCH0001.gif}} <<2426>>/<BR>TLC, plate: Silica gel 60 (Merck, 20 X 20 cm, 0.25 mm thick), solvent: 1st dim. chloroform - methanol - water (65:25:4, v/v), 2nd dim. n-butanol - acetic acid - water (6:2:2, v/v) <<2427>>,
	}}		}}

	{{Lipid/Footer}}		{{Lipid/Footer}}

Editor: LBGPEccp:R:R:ppppppppp:01 moved to LBGPEccp:R:R:p

2010-02-18T15:00:00Z

LBGPEccp:R:R:ppppppppp:01 moved to LBGPEccp:R:R:p

← Older revision		Revision as of 00:00, 19 February 2010
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	\|LipidBank=PGP2404		\|LipidBank=PGP2404
	\|SysName=1,2-di-acyl-sn-glycero- (3) -phospho-N,N-dimethylethanolamine		\|SysName=1,2-di-acyl-sn-glycero- (3) -phospho-N,N-dimethylethanolamine
	\|Common Name=phosphatidyl-N,N-~~dimethylethanolamineN~~,N-dimethylphosphatidylethanolamine 1,2-di-acyl-sn-glycero- (3) -phospho-N,N-dimethylethanolamine		\|Common Name=&&phosphatidyl-N,N-dimethylethanolamine&&N,N-dimethylphosphatidylethanolamine &&1,2-di-acyl-sn-glycero- (3) -phospho-N,N-dimethylethanolamine&&
	\|Melting Point=1,2-distearoyl-L-N,N-dimethylphosphatidylethanolamine, 168-169°C; 1,2-distearoyl-DL-N,N-dimethylphosphatidylethanolamine, 160-162°C; 1,2-dipalmitoyl-L-N,N-dimethylphosphatidylethanolamine, 164-165°C; 1,2-dipalmitoyl-DL-N,N-dimethylphosphatidylethanolamine, 160-161°C 2437		\|Melting Point=1,2-distearoyl-L-N,N-dimethylphosphatidylethanolamine, 168-169°C; 1,2-distearoyl-DL-N,N-dimethylphosphatidylethanolamine, 160-162°C; 1,2-dipalmitoyl-L-N,N-dimethylphosphatidylethanolamine, 164-165°C; 1,2-dipalmitoyl-DL-N,N-dimethylphosphatidylethanolamine, 160-161°C <<2437>>
	\|Reflactive=1,2-distearoyl-L-N-methylphosphatidylethanolamine, [FONT FACE=~~Symbola~~/FONT]~~subD~~/~~subsup25~~/sup +5.8°; 1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, [FONT FACE=~~Symbola~~/FONT]~~subD~~/~~subsup25~~/sup +5.8° 2437		\|Reflactive=1,2-distearoyl-L-N-methylphosphatidylethanolamine, [<FONT FACE="Symbol">a</FONT>]<sub>D</sub><sup>25</sup> +5.8°; 1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, [<FONT FACE="Symbol">a</FONT>]<sub>D</sub><sup>25</sup> +5.8° <<2437>>
	\|NMR Spectra=~~SUPFONT~~ SIZE=-12/FONT/~~SUPH~~-NMR spectra of PC, PDME, PMME, and PE fully hydrated with ~~DSUBFONT~~ SIZE=-12/FONT/~~SUBO~~ at the indicated temperatures {{Image200\|LBGPEccp:R:R:pSP0001.gif}} 2435.,		\|NMR Spectra=<SUP><FONT SIZE=-1>2</FONT></SUP>H-NMR spectra of PC, PDME, PMME, and PE fully hydrated with D<SUB><FONT SIZE=-1>2</FONT></SUB>O at the indicated temperatures {{Image200\|LBGPEccp:R:R:pSP0001.gif}} <<2435>>.,
	\|Chromatograms=HPLC, FONT FACE=~~Symbolm~~/~~FONTBondapak NHSUBFONT~~ SIZE=-12/FONT/SUB, acetonitril-methanol-water (13:7:1, v/v), elution rate 1.6 ml/min, detection ~~ODSUBFONT~~ SIZE=-12/FONT/~~SUBSUBFONT~~ SIZE=-10/FONT/~~SUBSUBFONT~~ SIZE=-13/FONT/SUB nm, Peaks: SF = solvent front, PC = phosphatidylcholine, SPH = sphingomyelin, LPC = lysophosphatidylcholine, PMME = phosphatidylmonomethylethanolamine, PE = phosphatidylethanolamine, PDME = phosphatidyldimethylethanolamine, LPE = lysophosphatidylethanolamine, {{Image200\|LBGPEccp:R:R:pCH0001.gif}} 2426/~~BRTLC~~, plate: Silica gel 60 (Merck, 20 X 20 cm, 0.25 mm thick), solvent: 1st dim. chloroform - methanol - water (65:25:4, v/v), 2nd dim. n-butanol - acetic acid - water (6:2:2, v/v) 2427,		\|Chromatograms=HPLC, <FONT FACE="Symbol">m</FONT>Bondapak NH<SUB><FONT SIZE=-1>2</FONT></SUB>, acetonitril-methanol-water (13:7:1, v/v), elution rate 1.6 ml/min, detection OD<SUB><FONT SIZE=-1>2</FONT></SUB><SUB><FONT SIZE=-1>0</FONT></SUB><SUB><FONT SIZE=-1>3</FONT></SUB> nm, Peaks: SF = solvent front, PC = phosphatidylcholine, SPH = sphingomyelin, LPC = lysophosphatidylcholine, PMME = phosphatidylmonomethylethanolamine, PE = phosphatidylethanolamine, PDME = phosphatidyldimethylethanolamine, LPE = lysophosphatidylethanolamine, {{Image200\|LBGPEccp:R:R:pCH0001.gif}} <<2426>>/<BR>TLC, plate: Silica gel 60 (Merck, 20 X 20 cm, 0.25 mm thick), solvent: 1st dim. chloroform - methanol - water (65:25:4, v/v), 2nd dim. n-butanol - acetic acid - water (6:2:2, v/v) <<2427>>,
	}}		}}

	{{Lipid/Footer}}		{{Lipid/Footer}}

Editor: LBGPEccp:R:R:ppppppppp:01 moved to LBGPEccp:R:R:p

2010-01-27T20:00:00Z

LBGPEccp:R:R:ppppppppp:01 moved to LBGPEccp:R:R:p

← Older revision		Revision as of 05:00, 28 January 2010
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	\|LipidBank=PGP2404		\|LipidBank=PGP2404
	\|SysName=1,2-di-acyl-sn-glycero- (3) -phospho-N,N-dimethylethanolamine		\|SysName=1,2-di-acyl-sn-glycero- (3) -phospho-N,N-dimethylethanolamine
	\|Common Name=&&phosphatidyl-N,N-~~dimethylethanolamine&&N~~,N-dimethylphosphatidylethanolamine &&1,2-di-acyl-sn-glycero- (3) -phospho-N,N-dimethylethanolamine&&		\|Common Name=phosphatidyl-N,N-dimethylethanolamineN,N-dimethylphosphatidylethanolamine 1,2-di-acyl-sn-glycero- (3) -phospho-N,N-dimethylethanolamine
	\|Melting Point=1,2-distearoyl-L-N,N-dimethylphosphatidylethanolamine, 168-169°C; 1,2-distearoyl-DL-N,N-dimethylphosphatidylethanolamine, 160-162°C; 1,2-dipalmitoyl-L-N,N-dimethylphosphatidylethanolamine, 164-165°C; 1,2-dipalmitoyl-DL-N,N-dimethylphosphatidylethanolamine, 160-161°C <<2437>>		\|Melting Point=1,2-distearoyl-L-N,N-dimethylphosphatidylethanolamine, 168-169°C; 1,2-distearoyl-DL-N,N-dimethylphosphatidylethanolamine, 160-162°C; 1,2-dipalmitoyl-L-N,N-dimethylphosphatidylethanolamine, 164-165°C; 1,2-dipalmitoyl-DL-N,N-dimethylphosphatidylethanolamine, 160-161°C 2437
	\|Reflactive=1,2-distearoyl-L-N-methylphosphatidylethanolamine, [<FONT FACE=~~"Symbol">a<~~/FONT>]~~<sub>D<~~/~~sub><sup>25<~~/sup> +5.8°; 1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, [<FONT FACE=~~"Symbol">a<~~/FONT>]~~<sub>D<~~/~~sub><sup>25<~~/sup> +5.8° <<2437>>		\|Reflactive=1,2-distearoyl-L-N-methylphosphatidylethanolamine, [FONT FACE=Symbola/FONT]subD/subsup25/sup +5.8°; 1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, [FONT FACE=Symbola/FONT]subD/subsup25/sup +5.8° 2437
	\|NMR Spectra=~~<SUP><FONT~~ SIZE=-~~1>2<~~/FONT></~~SUP>H~~-NMR spectra of PC, PDME, PMME, and PE fully hydrated with ~~D<SUB><FONT~~ SIZE=-~~1>2<~~/FONT></~~SUB>O~~ at the indicated temperatures {{Image200\|LBGPEccp:R:R:~~ppppppppp:01SP0001~~.gif}} <<2435>>.,		\|NMR Spectra=SUPFONT SIZE=-12/FONT/SUPH-NMR spectra of PC, PDME, PMME, and PE fully hydrated with DSUBFONT SIZE=-12/FONT/SUBO at the indicated temperatures {{Image200\|LBGPEccp:R:R:pSP0001.gif}} 2435.,
	\|Chromatograms=HPLC, <FONT FACE=~~"Symbol">m<~~/~~FONT>Bondapak NH<SUB><FONT~~ SIZE=-~~1>2<~~/FONT></SUB>, acetonitril-methanol-water (13:7:1, v/v), elution rate 1.6 ml/min, detection ~~OD<SUB><FONT~~ SIZE=-~~1>2<~~/FONT></~~SUB><SUB><FONT~~ SIZE=-~~1>0<~~/FONT></~~SUB><SUB><FONT~~ SIZE=-~~1>3<~~/FONT></SUB> nm, Peaks: SF = solvent front, PC = phosphatidylcholine, SPH = sphingomyelin, LPC = lysophosphatidylcholine, PMME = phosphatidylmonomethylethanolamine, PE = phosphatidylethanolamine, PDME = phosphatidyldimethylethanolamine, LPE = lysophosphatidylethanolamine, {{Image200\|LBGPEccp:R:R:~~ppppppppp:01CH0001~~.gif}} <<2426>>/~~<BR>TLC~~, plate: Silica gel 60 (Merck, 20 X 20 cm, 0.25 mm thick), solvent: 1st dim. chloroform - methanol - water (65:25:4, v/v), 2nd dim. n-butanol - acetic acid - water (6:2:2, v/v) <<2427>>,		\|Chromatograms=HPLC, FONT FACE=Symbolm/FONTBondapak NHSUBFONT SIZE=-12/FONT/SUB, acetonitril-methanol-water (13:7:1, v/v), elution rate 1.6 ml/min, detection ODSUBFONT SIZE=-12/FONT/SUBSUBFONT SIZE=-10/FONT/SUBSUBFONT SIZE=-13/FONT/SUB nm, Peaks: SF = solvent front, PC = phosphatidylcholine, SPH = sphingomyelin, LPC = lysophosphatidylcholine, PMME = phosphatidylmonomethylethanolamine, PE = phosphatidylethanolamine, PDME = phosphatidyldimethylethanolamine, LPE = lysophosphatidylethanolamine, {{Image200\|LBGPEccp:R:R:pCH0001.gif}} 2426/BRTLC, plate: Silica gel 60 (Merck, 20 X 20 cm, 0.25 mm thick), solvent: 1st dim. chloroform - methanol - water (65:25:4, v/v), 2nd dim. n-butanol - acetic acid - water (6:2:2, v/v) 2427,
	}}		}}

	{{Lipid/Footer}}		{{Lipid/Footer}}

Editor: LBGPEccp:R:R:ppppppppp:01 moved to LBGPEccp:R:R:p

2010-01-20T01:39:08Z

LBGPEccp:R:R:ppppppppp:01 moved to LBGPEccp:R:R:p

← Older revision	Revision as of 10:39, 20 January 2010
(No difference)

Editor at 13:00, 26 July 2009

2009-07-26T13:00:00Z

← Older revision		Revision as of 22:00, 26 July 2009
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			{{Lipid/Header}}

	{{Metabolite		{{Metabolite
	\|LipidBank=PGP2404		\|LipidBank=PGP2404
Line 8:		Line 10:
	\|Chromatograms=HPLC, <FONT FACE="Symbol">m</FONT>Bondapak NH<SUB><FONT SIZE=-1>2</FONT></SUB>, acetonitril-methanol-water (13:7:1, v/v), elution rate 1.6 ml/min, detection OD<SUB><FONT SIZE=-1>2</FONT></SUB><SUB><FONT SIZE=-1>0</FONT></SUB><SUB><FONT SIZE=-1>3</FONT></SUB> nm, Peaks: SF = solvent front, PC = phosphatidylcholine, SPH = sphingomyelin, LPC = lysophosphatidylcholine, PMME = phosphatidylmonomethylethanolamine, PE = phosphatidylethanolamine, PDME = phosphatidyldimethylethanolamine, LPE = lysophosphatidylethanolamine, {{Image200\|LBGPEccp:R:R:ppppppppp:01CH0001.gif}} <<2426>>/<BR>TLC, plate: Silica gel 60 (Merck, 20 X 20 cm, 0.25 mm thick), solvent: 1st dim. chloroform - methanol - water (65:25:4, v/v), 2nd dim. n-butanol - acetic acid - water (6:2:2, v/v) <<2427>>,		\|Chromatograms=HPLC, <FONT FACE="Symbol">m</FONT>Bondapak NH<SUB><FONT SIZE=-1>2</FONT></SUB>, acetonitril-methanol-water (13:7:1, v/v), elution rate 1.6 ml/min, detection OD<SUB><FONT SIZE=-1>2</FONT></SUB><SUB><FONT SIZE=-1>0</FONT></SUB><SUB><FONT SIZE=-1>3</FONT></SUB> nm, Peaks: SF = solvent front, PC = phosphatidylcholine, SPH = sphingomyelin, LPC = lysophosphatidylcholine, PMME = phosphatidylmonomethylethanolamine, PE = phosphatidylethanolamine, PDME = phosphatidyldimethylethanolamine, LPE = lysophosphatidylethanolamine, {{Image200\|LBGPEccp:R:R:ppppppppp:01CH0001.gif}} <<2426>>/<BR>TLC, plate: Silica gel 60 (Merck, 20 X 20 cm, 0.25 mm thick), solvent: 1st dim. chloroform - methanol - water (65:25:4, v/v), 2nd dim. n-butanol - acetic acid - water (6:2:2, v/v) <<2427>>,
	}}		}}

			{{Lipid/Footer}}

Editor at 12:00, 8 July 2009

2009-07-08T12:00:00Z

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{{Metabolite
|LipidBank=PGP2404
|SysName=1,2-di-acyl-sn-glycero- (3) -phospho-N,N-dimethylethanolamine
|Common Name=&&phosphatidyl-N,N-dimethylethanolamine&&N,N-dimethylphosphatidylethanolamine &&1,2-di-acyl-sn-glycero- (3) -phospho-N,N-dimethylethanolamine&&
|Melting Point=1,2-distearoyl-L-N,N-dimethylphosphatidylethanolamine, 168-169°C; 1,2-distearoyl-DL-N,N-dimethylphosphatidylethanolamine, 160-162°C; 1,2-dipalmitoyl-L-N,N-dimethylphosphatidylethanolamine, 164-165°C; 1,2-dipalmitoyl-DL-N,N-dimethylphosphatidylethanolamine, 160-161°C <<2437>>
|Reflactive=1,2-distearoyl-L-N-methylphosphatidylethanolamine, [a]D25 +5.8°; 1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, [a]D25 +5.8° <<2437>>
|NMR Spectra=2H-NMR spectra of PC, PDME, PMME, and PE fully hydrated with D2O at the indicated temperatures {{Image200|LBGPEccp:R:R:ppppppppp:01SP0001.gif}} <<2435>>.,
|Chromatograms=HPLC, mBondapak NH2, acetonitril-methanol-water (13:7:1, v/v), elution rate 1.6 ml/min, detection OD203 nm, Peaks: SF = solvent front, PC = phosphatidylcholine, SPH = sphingomyelin, LPC = lysophosphatidylcholine, PMME = phosphatidylmonomethylethanolamine, PE = phosphatidylethanolamine, PDME = phosphatidyldimethylethanolamine, LPE = lysophosphatidylethanolamine, {{Image200|LBGPEccp:R:R:ppppppppp:01CH0001.gif}} <<2426>>/ TLC, plate: Silica gel 60 (Merck, 20 X 20 cm, 0.25 mm thick), solvent: 1st dim. chloroform - methanol - water (65:25:4, v/v), 2nd dim. n-butanol - acetic acid - water (6:2:2, v/v) <<2427>>,
}}