LBGPEccp:R:R:YB2ANe001: Difference between revisions
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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 | |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, [ | |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= | |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, | |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}} |
Revision as of 14:00, 19 February 2010
LipidBank Top (トップ) |
Fatty acid (脂肪酸) |
Glycerolipid (グリセロ脂質) |
Sphingolipid (スフィンゴ脂質) |
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How to edit (ページの書き方) |
IDs and Links | |
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LipidBank | PGP2401 |
LipidMaps | [1] |
CAS | |
KEGG | {{{KEGG}}} |
KNApSAcK | {{{KNApSAcK}}} |
mol | LBGPEccp:R:R:YB2ANe001 |
phosphatidyl-N-methylethanolamine | |
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Structural Information | |
1,2-di-acyl-sn-glycero- (3) -phospho-N-methylethanolamine | |
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Formula | |
Exact Mass | |
Average Mass | |
SMILES | |
Physicochemical Information | |
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>> | |
Spectral Information | |
Mass Spectra | |
UV Spectra | |
IR Spectra | |
NMR Spectra | 2H-NMR spectra of PC, PDME, PMME, and PE fully hydrated with D2O at the indicated temperatures <<2410>>., |
Other Spectra | |
Chromatograms | HPLC, muBondapak 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, <<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>>, |
Reported Metabolites, References | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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