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MassBank Record: MSBNK-Chubu_Univ-UT002888

Phosphatidylethanolamine alkenyl 18:0-20:3; LC-ESI-ITFT; MS2; [M-H]-; RT: 34.38; Exp: 3

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

ACCESSION: MSBNK-Chubu_Univ-UT002888
RECORD_TITLE: Phosphatidylethanolamine alkenyl 18:0-20:3; LC-ESI-ITFT; MS2; [M-H]-; RT: 34.38; 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$NAME: Phosphatidylethanolamine alkenyl 18:0-20:3
CH$COMPOUND_CLASS: Natural Product; Glycerophospholipids; Glycerophosphoethanolamines; 1Z-alkenyl,2-acylglycerophosphoethanolamines
CH$FORMULA: C43H80NO7P
CH$EXACT_MASS: 753.56724
CH$SMILES: NCCOP(O)(=O)OCC(COC=CCCCCCCCCCCCCCCCC)OC(=O)CCC=CCC=CCC=CCCCCCCCCC
CH$IUPAC: InChI=1S/C43H80NO7P/c1-3-5-7-9-11-13-15-17-19-21-22-24-26-28-30-32-34-36-43(45)51-42(41-50-52(46,47)49-39-37-44)40-48-38-35-33-31-29-27-25-23-20-18-16-14-12-10-8-6-4-2/h19,21,24,26,30,32,35,38,42H,3-18,20,22-23,25,27-29,31,33-34,36-37,39-41,44H2,1-2H3,(H,46,47)/b21-19-,26-24-,32-30-,38-35+
CH$LINK: INCHIKEY IAZMKBZMIIUNID-DXSDZVOISA-N
SP$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$CHROMATOGRAPHY: RETENTION_TIME 34.60 min (in paper: 34.4 min)
AC$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$FOCUSED_ION: PRECURSOR_M/Z 752.56
MS$FOCUSED_ION: PRECURSOR_TYPE [M-H]-
MS$DATA_PROCESSING: WHOLE Xcalibur ver-2.0

PK$SPLASH: splash10-0a4i-0009200000-c95b09ebca030b65ed66
PK$ANNOTATION: m/z num type mass error(ppm) formula
  261.13 1 [fa(20:3)-H-CO2]- 261.2582260593 -490 C19H33-
  305.08 1 [fa(20:3)-H]- 305.2480553035 -550 C20H33O2-
  446.20 1 [lyso_PE(alkenyl-18:0,-)-H2O]- 446.3035350702 -231 C23H45NO5P-
  464.09 1 [lyso_PE(alkenyl-18:0,-)]- 464.3140997565 -482 C23H47NO6P-
  484.04 1 [lyso_PE(-,20:3)-H2O]- 484.2827996281 -500 C25H43NO6P-
PK$NUM_PEAK: 21
PK$PEAK: m/z int. rel.int.
  258.06 7.0 1
  261.13 59.4 7
  262.02 10.6 1
  266.82 7.7 1
  284.27 12.1 1
  287.24 26.7 3
  288.30 16.7 2
  289.25 15.0 2
  303.25 69.9 8
  305.08 8660.9 999
  306.24 1122.4 129
  307.28 14.5 2
  403.11 21.4 2
  437.37 5.3 1
  446.20 268.6 31
  447.21 39.0 4
  464.09 2208.9 255
  465.27 223.3 26
  466.49 21.8 3
  484.04 23.5 3
  578.45 12.1 1
//

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