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MassBank Record: MSBNK-Chubu_Univ-UT001394

Phosphatidylethanolamine 19:1-22:6; LC-ESI-ITFT; MS2; [M-H]-; RT: 19.66; Exp: 1

Mass Spectrum
Chemical Structure
Generated by the Chemistry Development Kit (http://github.com/cdk)

ACCESSION: MSBNK-Chubu_Univ-UT001394
RECORD_TITLE: Phosphatidylethanolamine 19:1-22:6; LC-ESI-ITFT; MS2; [M-H]-; RT: 19.66; Exp: 1
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$NAME: Phosphatidylethanolamine 19:1-22:6
CH$COMPOUND_CLASS: Natural Product; Glycerophospholipids; Glycerophosphoethanolamines; Diacylglycerophosphoethanolamines
CH$FORMULA: C46H78NO8P
CH$EXACT_MASS: 803.54650
CH$SMILES: C(CC=CCCCCCCCCCCCCCC)C(OCC(OC(=O)CCC=CCC=CCC=CCC=CCC=CCC=CCC)COP(O)(=O)OCCN)=O
CH$IUPAC: InChI=1S/C46H78NO8P/c1-3-5-7-9-11-13-15-17-19-21-22-23-25-27-29-31-33-35-37-39-46(49)55-44(43-54-56(50,51)53-41-40-47)42-52-45(48)38-36-34-32-30-28-26-24-20-18-16-14-12-10-8-6-4-2/h5,7,11,13,17,19,22-23,27,29,32-35,44H,3-4,6,8-10,12,14-16,18,20-21,24-26,28,30-31,36-43,47H2,1-2H3,(H,50,51)/b7-5-,13-11-,19-17-,23-22-,29-27-,34-32-,35-33-
CH$LINK: INCHIKEY ALIRENPDFGUYQE-NSLGBSSLSA-N
SP$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$CHROMATOGRAPHY: RETENTION_TIME 19.65 min (in paper: 19.7 min)
AC$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$FOCUSED_ION: PRECURSOR_M/Z 802.54
MS$FOCUSED_ION: PRECURSOR_TYPE [M-H]-
MS$DATA_PROCESSING: WHOLE Xcalibur ver-2.0

PK$SPLASH: splash10-002g-0096300700-be2268aa06afff5cc1e0
PK$ANNOTATION: m/z num type mass error(ppm) formula
  283.08 1 [fa(22:6)-H-CO2]- 283.2425759951 -573 C21H31-
  295.10 1 [fa(19:1)-H]- 295.2637053677 -553 C19H35O2-
  327.05 1 [fa(22:6)-H]- 327.2324052393 -556 C22H31O2-
  492.05 1 [lyso_PE(19:1,-)]- 492.3090143786 -525 C24H47NO7P-
PK$NUM_PEAK: 24
PK$PEAK: m/z int. rel.int.
  281.08 29.1 50
  282.08 7.2 12
  283.08 210.9 361
  284.25 49.7 85
  285.19 16.2 28
  295.10 430.6 736
  296.21 69.0 118
  305.08 5.6 10
  309.21 46.8 80
  310.13 10.1 17
  311.04 23.1 40
  327.05 406.8 696
  327.94 112.5 192
  492.05 317.7 543
  492.90 24.9 43
  505.91 6.2 11
  539.23 17.9 31
  714.20 14.2 24
  715.15 19.3 33
  727.11 12.6 22
  740.99 7.5 13
  742.07 584.2 999
  743.01 24.1 41
  769.86 8.6 15
//

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