MassBank Record: UT002105



 Phosphatidylethanolamine 16:0-22:6; LC-ESI-ITFT; MS2; [M-H]-; RT: 17.45; Exp: 2 
Mass Spectrum
Chemical Structure
Generated by the Chemistry Development Kit (http://github.com/cdk) \n

ACCESSION: UT002105
RECORD_TITLE: Phosphatidylethanolamine 16:0-22:6; LC-ESI-ITFT; MS2; [M-H]-; RT: 17.45; Exp: 2
DATE: 2016.01.19 (Created 2010.05.07, modified 2011.08.03)
AUTHORS: Taguchi R, Graduate School of Medicine, The University of Tokyo.
LICENSE: CC BY-NC-SA
PUBLICATION: Taguchi, R.; Ishikawa M.; Precise and global identification of phospholipid molecular species by an Orbitrap mass spectrometer and automated search engine Lipid Search. J Chromatogr A (2010), doi:10.1016/j.chroma.2010.04.034 (in press)

CH$NAME: Phosphatidylethanolamine 16:0-22:6 CH$COMPOUND_CLASS: Natural Product; Glycerophospholipids; Glycerophosphoethanolamines; Diacylglycerophosphoethanolamines CH$FORMULA: C43H74NO8P CH$EXACT_MASS: 763.51520 CH$SMILES: OP(=O)(OCCN)OCC(COC(=O)CCCCCCCCCCCCCCC)OC(=O)CCC=CCC=CCC=CCC=CCC=CCC=CCC CH$IUPAC: InChI=1S/C43H74NO8P/c1-3-5-7-9-11-13-15-17-18-19-20-21-22-24-26-28-30-32-34-36-43(46)52-41(40-51-53(47,48)50-38-37-44)39-49-42(45)35-33-31-29-27-25-23-16-14-12-10-8-6-4-2/h5,7,11,13,17-18,20-21,24,26,30,32,41H,3-4,6,8-10,12,14-16,19,22-23,25,27-29,31,33-40,44H2,1-2H3,(H,47,48)/b7-5-,13-11-,18-17-,21-20-,26-24-,32-30- CH$LINK: CAS 202647-79-8 SP$SCIENTIFIC_NAME: Mus musculus SP$NAME: mouse SP$LINEAGE: cellular organisms; Eukaryota; Fungi/Metazoa group; Metazoa; Eumetazoa; Bilateria; Coelomata; Deuterostomia; Chordata; Craniata; Vertebrata; Gnathostomata; Teleostomi; Euteleostomi; Sarcopterygii; Tetrapoda; Amniota; Mammalia; Theria; Eutheria; Euarchontoglires; Glires; Rodentia; Sciurognathi; Muroidea; Muridae; Murinae; Mus SP$LINK: NCBI-TAXONOMY 10090 SP$SAMPLE: brain
AC$INSTRUMENT: LC-10ADVPmicro HPLC, Shimadzu; LTQ Orbitrap, Thermo Scientific AC$INSTRUMENT_TYPE: LC-ESI-ITFT AC$MASS_SPECTROMETRY: MS_TYPE MS2 AC$MASS_SPECTROMETRY: ION_MODE NEGATIVE AC$MASS_SPECTROMETRY: COLLISION_ENERGY 30% AC$MASS_SPECTROMETRY: ION_SPRAY_VOLTAGE 3500 V AC$MASS_SPECTROMETRY: IONIZATION ESI AC$CHROMATOGRAPHY: COLUMN_NAME Develosil C30, Nomura Chemical AC$CHROMATOGRAPHY: FLOW_GRADIENT add 95/5 at 0 min, 70/30 at 40 min, 50/50 at 41 min, 50/50 at 90 min AC$CHROMATOGRAPHY: FLOW_RATE add 100 uL/min AC$CHROMATOGRAPHY: RETENTION_TIME 17.62 min (in paper: 17.5 min) AC$CHROMATOGRAPHY: SOLVENT A acetonitrile-methanol-water (19:19:2) with 0.1% acetic acid and 0.1% ammonium hydroxide (28%) AC$CHROMATOGRAPHY: SOLVENT B 2-propanol with 0.1% acetic acid and 0.1% ammonium hydroxide (28%)
MS$FOCUSED_ION: PRECURSOR_M/Z 762.51 MS$FOCUSED_ION: PRECURSOR_TYPE [M-H]- MS$DATA_PROCESSING: WHOLE Xcalibur ver-2.0
PK$SPLASH: splash10-057i-0096300000-61062deba5e37d95d6b0 PK$ANNOTATION: m/z num ( type mass error(ppm) formula ) 524.05 1 [lyso PE(-,22:6)]- 524.2777142502 -433 C27H43NO7P- 506.24 1 [lyso PE(-,22:6)-H2O]- 506.2671495639 -53 C27H41NO6P- 452.06 1 [lyso PE(16:0,-)]- 452.2777142502 -480 C21H43NO7P- 434.18 1 [lyso PE(16:0,-)-H2O]- 434.2671495639 -200 C21H41NO6P- 327.05 1 [fa(22:6)-H]- 327.2324052393 -556 C22H31O2- 283.12 1 [fa(22:6)-H-CO2]- 283.2425759951 -432 C21H31- 255.07 1 [fa(16:0)-H]- 255.2324052393 -635 C16H31O2- PK$NUM_PEAK: 29 PK$PEAK: m/z int. rel.int. 229.08 1170.1 30 230.19 76.0 2 238.74 87.8 2 249.05 1274.8 32 255.07 26921.4 680 256.17 2156.0 54 257.17 70.5 2 266.66 65.5 2 270.85 98.4 2 273.25 106.6 3 283.12 24843.6 627 284.12 1665.7 42 309.13 270.6 7 327.05 39561.4 999 328.05 5094.4 129 378.32 87.9 2 383.32 169.9 4 390.50 156.2 4 434.18 989.2 25 437.40 72.3 2 452.06 20376.5 515 453.20 900.9 23 464.22 115.1 3 505.19 183.7 5 506.24 616.7 16 506.89 37.6 1 524.05 1786.6 45 525.11 354.2 9 762.15 44.4 1 //