ACCESSION: MSBNK-Chubu_Univ-UT002871
RECORD_TITLE: Phosphatidylethanolamine 22:6-24:6; LC-ESI-ITFT; MS2; [M-H]-; RT: 12.75; Exp: 3
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. Journal of Chromatography A 2010, 1217 (25), 4229–39. DOI:10.1016/j.chroma.2010.04.034
CH$NAME: Phosphatidylethanolamine 22:6-24:6
CH$COMPOUND_CLASS: Natural Product; Glycerophospholipids; Glycerophosphoethanolamines; Diacylglycerophosphoethanolamines
CH$FORMULA: C51H78NO8P
CH$EXACT_MASS: 863.54650
CH$SMILES: C(C(COC(=O)CCC=CCC=CCC=CCC=CCC=CCC=CCC)OC(CCC=CCC=CCC=CCC=CCC=CCC=CCCCC)=O)OP(O)(=O)OCCN
CH$IUPAC: InChI=1S/C51H78NO8P/c1-3-5-7-9-11-13-15-17-19-21-23-24-26-28-30-32-34-36-38-40-42-44-51(54)60-49(48-59-61(55,56)58-46-45-52)47-57-50(53)43-41-39-37-35-33-31-29-27-25-22-20-18-16-14-12-10-8-6-4-2/h6,8-9,11-12,14-15,17-18,20-21,23,25-28,31-34,37-40,49H,3-5,7,10,13,16,19,22,24,29-30,35-36,41-48,52H2,1-2H3,(H,55,56)/b8-6-,11-9-,14-12-,17-15-,20-18-,23-21-,27-25-,28-26-,33-31-,34-32-,39-37-,40-38-
CH$LINK: INCHIKEY
RYRYLVYZMTURGB-RIJNFFOPSA-N
SP$SCIENTIFIC_NAME: Mus musculus
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 12.81 min (in paper: 12.8 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$FOCUSED_ION: PRECURSOR_M/Z 862.54
MS$FOCUSED_ION: PRECURSOR_TYPE [M-H]-
MS$DATA_PROCESSING: WHOLE Xcalibur ver-2.0
PK$SPLASH: splash10-0pdr-0019030200-2907fb28f5aa90da95b6
PK$ANNOTATION: m/z num type mass error(ppm) formula
283.22 1 [fa(22:6)-H-CO2]- 283.2425759951 -79 C21H31-
311.07 1 [fa(24:6)-H-CO2]- 311.2738761235 -654 C23H35-
327.23 1 [fa(22:6)-H]- 327.2324052393 -6 C22H31O2-
355.05 1 [fa(24:6)-H]- 355.2637053677 -601 C24H35O2-
552.06 1 [lyso_PE(-,24:6)]- 552.3090143786 -450 C29H47NO7P-
PK$NUM_PEAK: 15
PK$PEAK: m/z int. rel.int.
267.86 11.9 73
283.22 62.0 380
311.07 36.0 221
312.13 7.2 44
327.23 160.2 981
328.23 7.8 48
355.05 163.1 999
356.20 18.3 112
506.91 6.1 37
552.06 116.4 713
553.15 48.9 300
685.78 10.8 66
697.76 5.5 34
788.21 105.6 647
825.27 4.4 27
//
