LBGPEccp:R:R:YB2ANe001 - Revision history

Editor: LBGPEccp:R:R:YB2ANe001:01 moved to LBGPEccp:R:R:YB2ANe001

2010-04-14T21:00:00Z

LBGPEccp:R:R:YB2ANe001:01 moved to LBGPEccp:R:R:YB2ANe001

← Older revision		Revision as of 06:00, 15 April 2010
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	\|LipidBank=PGP2401		\|LipidBank=PGP2401
	\|SysName=1,2-di-acyl-sn-glycero- (3) -phospho-N-methylethanolamine		\|SysName=1,2-di-acyl-sn-glycero- (3) -phospho-N-methylethanolamine
	\|Common Name=&&phosphatidyl-N-methylethanolamine&& N-methylphosphatidylethanolamine&&phosphatidyl-N-monomethylethanolamine~~&&1,2-di-acyl-sn-glycero- (3) -phospho-N-methylethanolamine~~&&		\|Common Name=&&phosphatidyl-N-methylethanolamine&&N-methylphosphatidylethanolamine&&phosphatidyl-N-monomethylethanolamine&&
	\|Melting Point=1,2-distearoyl-L-N-methylphosphatidylethanolamine, 178-180°C <<2412>>; 1,2-distearoyl-DL-N-methylphosphatidylethanolamine, 171-172°C <<2412>>; 1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, 177-178°C <<2412>>, 184-186°C (from CHCl_3 -MeOH at 4°C <<2413>>; 1,2-dipalmitoyl-DL-N-methylphosphatidylethanolamine, 170-171°C <<2412>>, 182°C <<2413>>		\|Melting Point=1,2-distearoyl-L-N-methylphosphatidylethanolamine, 178-180°C <<2412>>; 1,2-distearoyl-DL-N-methylphosphatidylethanolamine, 171-172°C <<2412>>; 1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, 177-178°C <<2412>>, 184-186°C (from CHCl_3 -MeOH at 4°C <<2413>>; 1,2-dipalmitoyl-DL-N-methylphosphatidylethanolamine, 170-171°C <<2412>>, 182°C <<2413>>
	\|Reflactive=1,2-distearoyl-L-N-methylphosphatidylethanolamine, [ alpha ]^{25}_D +7.1° <<2412>>; 1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, [ alpha ]^{25}_D +8.0° <<2412>>, [ alpha ]^{23}_D +8.0° (in CHCl_3 ) <<2413>>		\|Reflactive=1,2-distearoyl-L-N-methylphosphatidylethanolamine, [ alpha ]^{25}_D +7.1° <<2412>>; 1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, [ alpha ]^{25}_D +8.0° <<2412>>, [ alpha ]^{23}_D +8.0° (in CHCl_3 ) <<2413>>

Editor: LBGPEccp:R:R:YB2ANe001:01 moved to LBGPEccp:R:R:YB2ANe001

2010-02-25T10:00:10Z

LBGPEccp:R:R:YB2ANe001:01 moved to LBGPEccp:R:R:YB2ANe001

← Older revision		Revision as of 19:00, 25 February 2010
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	\|Common Name=&&phosphatidyl-N-methylethanolamine&& N-methylphosphatidylethanolamine&&phosphatidyl-N-monomethylethanolamine&&1,2-di-acyl-sn-glycero- (3) -phospho-N-methylethanolamine&&		\|Common Name=&&phosphatidyl-N-methylethanolamine&& N-methylphosphatidylethanolamine&&phosphatidyl-N-monomethylethanolamine&&1,2-di-acyl-sn-glycero- (3) -phospho-N-methylethanolamine&&
	\|Melting Point=1,2-distearoyl-L-N-methylphosphatidylethanolamine, 178-180°C <<2412>>; 1,2-distearoyl-DL-N-methylphosphatidylethanolamine, 171-172°C <<2412>>; 1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, 177-178°C <<2412>>, 184-186°C (from CHCl_3 -MeOH at 4°C <<2413>>; 1,2-dipalmitoyl-DL-N-methylphosphatidylethanolamine, 170-171°C <<2412>>, 182°C <<2413>>		\|Melting Point=1,2-distearoyl-L-N-methylphosphatidylethanolamine, 178-180°C <<2412>>; 1,2-distearoyl-DL-N-methylphosphatidylethanolamine, 171-172°C <<2412>>; 1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, 177-178°C <<2412>>, 184-186°C (from CHCl_3 -MeOH at 4°C <<2413>>; 1,2-dipalmitoyl-DL-N-methylphosphatidylethanolamine, 170-171°C <<2412>>, 182°C <<2413>>
	\|Reflactive=1,2-distearoyl-L-N-methylphosphatidylethanolamine, [ alpha ]^~~25_D~~ +7.1° <<2412>>; 1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, [ alpha ]^~~25_D~~ +8.0° <<2412>>, [ alpha ]^~~23_D~~ +8.0° (in CHCl_3 ) <<2413>>		\|Reflactive=1,2-distearoyl-L-N-methylphosphatidylethanolamine, [ alpha ]^{25}_D +7.1° <<2412>>; 1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, [ alpha ]^{25}_D +8.0° <<2412>>, [ alpha ]^{23}_D +8.0° (in CHCl_3 ) <<2413>>
	\|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:YB2ANe001SP0001.gif}} <<2410>>.,		\|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:YB2ANe001SP0001.gif}} <<2410>>.,
	\|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:YB2ANe001CH0001.gif}} <<2401>>/<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) <<2402>>,		\|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:YB2ANe001CH0001.gif}} <<2401>>/<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) <<2402>>,
	}}		}}

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

Editor: LBGPEccp:R:R:YB2ANe001:01 moved to LBGPEccp:R:R:YB2ANe001

2010-02-19T14:00:10Z

LBGPEccp:R:R:YB2ANe001:01 moved to LBGPEccp:R:R:YB2ANe001

← Older revision		Revision as of 23:00, 19 February 2010
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	\|Common Name=&&phosphatidyl-N-methylethanolamine&& N-methylphosphatidylethanolamine&&phosphatidyl-N-monomethylethanolamine&&1,2-di-acyl-sn-glycero- (3) -phospho-N-methylethanolamine&&		\|Common Name=&&phosphatidyl-N-methylethanolamine&& N-methylphosphatidylethanolamine&&phosphatidyl-N-monomethylethanolamine&&1,2-di-acyl-sn-glycero- (3) -phospho-N-methylethanolamine&&
	\|Melting Point=1,2-distearoyl-L-N-methylphosphatidylethanolamine, 178-180°C <<2412>>; 1,2-distearoyl-DL-N-methylphosphatidylethanolamine, 171-172°C <<2412>>; 1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, 177-178°C <<2412>>, 184-186°C (from CHCl_3 -MeOH at 4°C <<2413>>; 1,2-dipalmitoyl-DL-N-methylphosphatidylethanolamine, 170-171°C <<2412>>, 182°C <<2413>>		\|Melting Point=1,2-distearoyl-L-N-methylphosphatidylethanolamine, 178-180°C <<2412>>; 1,2-distearoyl-DL-N-methylphosphatidylethanolamine, 171-172°C <<2412>>; 1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, 177-178°C <<2412>>, 184-186°C (from CHCl_3 -MeOH at 4°C <<2413>>; 1,2-dipalmitoyl-DL-N-methylphosphatidylethanolamine, 170-171°C <<2412>>, 182°C <<2413>>
	\|Reflactive=1,2-distearoyl-L-N-methylphosphatidylethanolamine, [alpha]^25_D +7.1° <<2412>>; 1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, [alpha]^25_D +8.0° <<2412>>, [alpha]^23_D +8.0° (in CHCl_3 ) <<2413>>		\|Reflactive=1,2-distearoyl-L-N-methylphosphatidylethanolamine, [ alpha ]^25_D +7.1° <<2412>>; 1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, [ alpha ]^25_D +8.0° <<2412>>, [ alpha ]^23_D +8.0° (in CHCl_3 ) <<2413>>
	\|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:YB2ANe001SP0001.gif}} <<2410>>.,		\|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:YB2ANe001SP0001.gif}} <<2410>>.,
	\|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:YB2ANe001CH0001.gif}} <<2401>>/<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) <<2402>>,		\|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:YB2ANe001CH0001.gif}} <<2401>>/<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) <<2402>>,
	}}		}}

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

Editor: LBGPEccp:R:R:YB2ANe001:01 moved to LBGPEccp:R:R:YB2ANe001

2010-02-19T14:00:00Z

LBGPEccp:R:R:YB2ANe001:01 moved to LBGPEccp:R:R:YB2ANe001

← Older revision		Revision as of 23:00, 19 February 2010
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	\|SysName=1,2-di-acyl-sn-glycero- (3) -phospho-N-methylethanolamine		\|SysName=1,2-di-acyl-sn-glycero- (3) -phospho-N-methylethanolamine
	\|Common Name=&&phosphatidyl-N-methylethanolamine&& N-methylphosphatidylethanolamine&&phosphatidyl-N-monomethylethanolamine&&1,2-di-acyl-sn-glycero- (3) -phospho-N-methylethanolamine&&		\|Common Name=&&phosphatidyl-N-methylethanolamine&& N-methylphosphatidylethanolamine&&phosphatidyl-N-monomethylethanolamine&&1,2-di-acyl-sn-glycero- (3) -phospho-N-methylethanolamine&&
	\|Melting Point=1,2-distearoyl-L-N-methylphosphatidylethanolamine, 178-180°C <<2412>>; 1,2-distearoyl-DL-N-methylphosphatidylethanolamine, 171-172°C <<2412>>; 1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, 177-178°C <<2412>>, 184-186°C (from ~~CHCl<SUB><FONT SIZE=-1>3</FONT></SUB>~~-MeOH at 4°C <<2413>>; 1,2-dipalmitoyl-DL-N-methylphosphatidylethanolamine, 170-171°C <<2412>>, 182°C <<2413>>		\|Melting Point=1,2-distearoyl-L-N-methylphosphatidylethanolamine, 178-180°C <<2412>>; 1,2-distearoyl-DL-N-methylphosphatidylethanolamine, 171-172°C <<2412>>; 1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, 177-178°C <<2412>>, 184-186°C (from CHCl_3 -MeOH at 4°C <<2413>>; 1,2-dipalmitoyl-DL-N-methylphosphatidylethanolamine, 170-171°C <<2412>>, 182°C <<2413>>
	\|Reflactive=1,2-distearoyl-L-N-methylphosphatidylethanolamine, [~~<FONT FACE="Symbol">a</FONT>~~]~~<sub>D</sub><sup>25</sup>~~ +7.1° <<2412>>; 1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, [~~<FONT FACE="Symbol">a</FONT>~~]~~<sub>D</sub><sup>25</sup>~~ +8.0° <<2412>>, [~~<FONT FACE="Symbol">a</FONT>~~]~~<sub>D</sub><sup>23</sup>~~ +8.0° (in ~~CHCl<SUB><FONT SIZE=-1>3</FONT></SUB>~~) <<2413>>		\|Reflactive=1,2-distearoyl-L-N-methylphosphatidylethanolamine, [alpha]^25_D +7.1° <<2412>>; 1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, [alpha]^25_D +8.0° <<2412>>, [alpha]^23_D +8.0° (in CHCl_3 ) <<2413>>
	\|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:YB2ANe001SP0001.gif}} <<2410>>.,		\|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:YB2ANe001SP0001.gif}} <<2410>>.,
	\|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:YB2ANe001CH0001.gif}} <<2401>>/<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) <<2402>>,		\|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:YB2ANe001CH0001.gif}} <<2401>>/<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) <<2402>>,
	}}		}}

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

Editor: LBGPEccp:R:R:YB2ANe001:01 moved to LBGPEccp:R:R:YB2ANe001

2010-02-18T15:00:00Z

LBGPEccp:R:R:YB2ANe001:01 moved to LBGPEccp:R:R:YB2ANe001

← Older revision		Revision as of 00:00, 19 February 2010
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	\|LipidBank=PGP2401		\|LipidBank=PGP2401
	\|SysName=1,2-di-acyl-sn-glycero- (3) -phospho-N-methylethanolamine		\|SysName=1,2-di-acyl-sn-glycero- (3) -phospho-N-methylethanolamine
	\|Common Name=phosphatidyl-N-methylethanolamine N-~~methylphosphatidylethanolaminephosphatidyl~~-N-~~monomethylethanolamine1~~,2-di-acyl-sn-glycero- (3) -phospho-N-methylethanolamine		\|Common Name=&&phosphatidyl-N-methylethanolamine&& N-methylphosphatidylethanolamine&&phosphatidyl-N-monomethylethanolamine&&1,2-di-acyl-sn-glycero- (3) -phospho-N-methylethanolamine&&
	\|Melting Point=1,2-distearoyl-L-N-methylphosphatidylethanolamine, 178-180°C 2412; 1,2-distearoyl-DL-N-methylphosphatidylethanolamine, 171-172°C 2412; 1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, 177-178°C 2412, 184-186°C (from ~~CHClSUBFONT~~ SIZE=-13/FONT/SUB-MeOH at 4°C 2413; 1,2-dipalmitoyl-DL-N-methylphosphatidylethanolamine, 170-171°C 2412, 182°C 2413		\|Melting Point=1,2-distearoyl-L-N-methylphosphatidylethanolamine, 178-180°C <<2412>>; 1,2-distearoyl-DL-N-methylphosphatidylethanolamine, 171-172°C <<2412>>; 1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, 177-178°C <<2412>>, 184-186°C (from CHCl<SUB><FONT SIZE=-1>3</FONT></SUB>-MeOH at 4°C <<2413>>; 1,2-dipalmitoyl-DL-N-methylphosphatidylethanolamine, 170-171°C <<2412>>, 182°C <<2413>>
	\|Reflactive=1,2-distearoyl-L-N-methylphosphatidylethanolamine, [FONT FACE=~~Symbola~~/FONT]~~subD~~/~~subsup25~~/sup +7.1° 2412; 1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, [FONT FACE=~~Symbola~~/FONT]~~subD~~/~~subsup25~~/sup +8.0° 2412, [FONT FACE=~~Symbola~~/FONT]~~subD~~/~~subsup23~~/sup +8.0° (in ~~CHClSUBFONT~~ SIZE=-13/FONT/SUB) 2413		\|Reflactive=1,2-distearoyl-L-N-methylphosphatidylethanolamine, [<FONT FACE="Symbol">a</FONT>]<sub>D</sub><sup>25</sup> +7.1° <<2412>>; 1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, [<FONT FACE="Symbol">a</FONT>]<sub>D</sub><sup>25</sup> +8.0° <<2412>>, [<FONT FACE="Symbol">a</FONT>]<sub>D</sub><sup>23</sup> +8.0° (in CHCl<SUB><FONT SIZE=-1>3</FONT></SUB>) <<2413>>
	\|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:YB2ANe001SP0001.gif}} 2410.,		\|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:YB2ANe001SP0001.gif}} <<2410>>.,
	\|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:YB2ANe001CH0001.gif}} 2401/~~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) 2402,		\|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:YB2ANe001CH0001.gif}} <<2401>>/<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) <<2402>>,
	}}		}}

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

Editor: LBGPEccp:R:R:YB2ANe001:01 moved to LBGPEccp:R:R:YB2ANe001

2010-01-27T20:00:00Z

LBGPEccp:R:R:YB2ANe001:01 moved to LBGPEccp:R:R:YB2ANe001

← Older revision		Revision as of 05:00, 28 January 2010
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	\|LipidBank=PGP2401		\|LipidBank=PGP2401
	\|SysName=1,2-di-acyl-sn-glycero- (3) -phospho-N-methylethanolamine		\|SysName=1,2-di-acyl-sn-glycero- (3) -phospho-N-methylethanolamine
	\|Common Name=&&phosphatidyl-N-methylethanolamine&& N-~~methylphosphatidylethanolamine&&phosphatidyl~~-N-~~monomethylethanolamine&&1~~,2-di-acyl-sn-glycero- (3) -phospho-N-methylethanolamine&&		\|Common Name=phosphatidyl-N-methylethanolamine N-methylphosphatidylethanolaminephosphatidyl-N-monomethylethanolamine1,2-di-acyl-sn-glycero- (3) -phospho-N-methylethanolamine
	\|Melting Point=1,2-distearoyl-L-N-methylphosphatidylethanolamine, 178-180°C <<2412>>; 1,2-distearoyl-DL-N-methylphosphatidylethanolamine, 171-172°C <<2412>>; 1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, 177-178°C <<2412>>, 184-186°C (from ~~CHCl<SUB><FONT~~ SIZE=-~~1>3<~~/FONT></SUB>-MeOH at 4°C <<2413>>; 1,2-dipalmitoyl-DL-N-methylphosphatidylethanolamine, 170-171°C <<2412>>, 182°C <<2413>>		\|Melting Point=1,2-distearoyl-L-N-methylphosphatidylethanolamine, 178-180°C 2412; 1,2-distearoyl-DL-N-methylphosphatidylethanolamine, 171-172°C 2412; 1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, 177-178°C 2412, 184-186°C (from CHClSUBFONT SIZE=-13/FONT/SUB-MeOH at 4°C 2413; 1,2-dipalmitoyl-DL-N-methylphosphatidylethanolamine, 170-171°C 2412, 182°C 2413
	\|Reflactive=1,2-distearoyl-L-N-methylphosphatidylethanolamine, [<FONT FACE=~~"Symbol">a<~~/FONT>]~~<sub>D<~~/~~sub><sup>25<~~/sup> +7.1° <<2412>>; 1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, [<FONT FACE=~~"Symbol">a<~~/FONT>]~~<sub>D<~~/~~sub><sup>25<~~/sup> +8.0° <<2412>>, [<FONT FACE=~~"Symbol">a<~~/FONT>]~~<sub>D<~~/~~sub><sup>23<~~/sup> +8.0° (in ~~CHCl<SUB><FONT~~ SIZE=-~~1>3<~~/FONT></SUB>) <<2413>>		\|Reflactive=1,2-distearoyl-L-N-methylphosphatidylethanolamine, [FONT FACE=Symbola/FONT]subD/subsup25/sup +7.1° 2412; 1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, [FONT FACE=Symbola/FONT]subD/subsup25/sup +8.0° 2412, [FONT FACE=Symbola/FONT]subD/subsup23/sup +8.0° (in CHClSUBFONT SIZE=-13/FONT/SUB) 2413
	\|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:~~YB2ANe001:01SP0001~~.gif}} <<2410>>.,		\|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:YB2ANe001SP0001.gif}} 2410.,
	\|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:~~YB2ANe001:01CH0001~~.gif}} <<2401>>/~~<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) <<2402>>,		\|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:YB2ANe001CH0001.gif}} 2401/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) 2402,
	}}		}}

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

Editor: LBGPEccp:R:R:YB2ANe001:01 moved to LBGPEccp:R:R:YB2ANe001

2010-01-20T01:39:08Z

LBGPEccp:R:R:YB2ANe001:01 moved to LBGPEccp:R:R:YB2ANe001

← 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=PGP2401		\|LipidBank=PGP2401
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	\|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:YB2ANe001:01CH0001.gif}} <<2401>>/<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) <<2402>>,		\|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:YB2ANe001:01CH0001.gif}} <<2401>>/<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) <<2402>>,
	}}		}}

			{{Lipid/Footer}}

Editor at 12:00, 8 July 2009

2009-07-08T12:00:00Z

New page

{{Metabolite
|LipidBank=PGP2401
|SysName=1,2-di-acyl-sn-glycero- (3) -phospho-N-methylethanolamine
|Common Name=&&phosphatidyl-N-methylethanolamine&& N-methylphosphatidylethanolamine&&phosphatidyl-N-monomethylethanolamine&&1,2-di-acyl-sn-glycero- (3) -phospho-N-methylethanolamine&&
|Melting Point=1,2-distearoyl-L-N-methylphosphatidylethanolamine, 178-180°C <<2412>>; 1,2-distearoyl-DL-N-methylphosphatidylethanolamine, 171-172°C <<2412>>; 1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, 177-178°C <<2412>>, 184-186°C (from CHCl3-MeOH at 4°C <<2413>>; 1,2-dipalmitoyl-DL-N-methylphosphatidylethanolamine, 170-171°C <<2412>>, 182°C <<2413>>
|Reflactive=1,2-distearoyl-L-N-methylphosphatidylethanolamine, [a]D25 +7.1° <<2412>>; 1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, [a]D25 +8.0° <<2412>>, [a]D23 +8.0° (in CHCl3) <<2413>>
|NMR Spectra=2H-NMR spectra of PC, PDME, PMME, and PE fully hydrated with D2O at the indicated temperatures {{Image200|LBGPEccp:R:R:YB2ANe001:01SP0001.gif}} <<2410>>.,
|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:YB2ANe001:01CH0001.gif}} <<2401>>/ 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) <<2402>>,
}}