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MassBank Record: MSBNK-Chubu_Univ-UT002889

Phosphatidylethanolamine alkenyl 18:0-20:4; LC-ESI-ITFT; MS2; [M-H]-; RT: 30.78; Exp: 3

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

ACCESSION: MSBNK-Chubu_Univ-UT002889
RECORD_TITLE: Phosphatidylethanolamine alkenyl 18:0-20:4; LC-ESI-ITFT; MS2; [M-H]-; RT: 30.78; 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$NAME: Phosphatidylethanolamine alkenyl 18:0-20:4
CH$COMPOUND_CLASS: Natural Product; Glycerophospholipids; Glycerophosphoethanolamines; 1Z-alkenyl,2-acylglycerophosphoethanolamines
CH$FORMULA: C43H78NO7P
CH$EXACT_MASS: 751.55159
CH$SMILES: NCCOP(O)(=O)OCC(COC=CCCCCCCCCCCCCCCCC)OC(=O)CCC=CCC=CCC=CCC=CCCCCCC
CH$IUPAC: InChI=1S/C43H78NO7P/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/h13,15,19,21,24,26,30,32,35,38,42H,3-12,14,16-18,20,22-23,25,27-29,31,33-34,36-37,39-41,44H2,1-2H3,(H,46,47)/b15-13-,21-19-,26-24-,32-30-,38-35+
CH$LINK: INCHIKEY RZZGAMUARHRLJN-ZOWVHDLQSA-N
SP$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$CHROMATOGRAPHY: RETENTION_TIME 30.94 min (in paper: 30.5 min)
AC$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$FOCUSED_ION: PRECURSOR_M/Z 750.54
MS$FOCUSED_ION: PRECURSOR_TYPE [M-H]-
MS$DATA_PROCESSING: WHOLE Xcalibur ver-2.0

PK$SPLASH: splash10-0udi-0009400000-d7fb911b4594c2d97fe4
PK$ANNOTATION: m/z num type mass error(ppm) formula
  259.07 1 [fa(20:4)-H-CO2]- 259.2425759951 -665 C19H31-
  267.38 1 [fa(alkenyl-18:0)-H]- 267.2687907456 416 C18H35O-
  303.04 1 [fa(20:4)-H]- 303.2324052393 -634 C20H31O2-
  446.16 1 [lyso_PE(alkenyl-18:0,-)-H2O]- 446.3035350702 -321 C23H45NO5P-
  464.21 1 [lyso_PE(alkenyl-18:0,-)]- 464.3140997565 -223 C23H47NO6P-
  482.15 1 [lyso_PE(-,20:4)-H2O]- 482.2671495639 -242 C25H41NO6P-
PK$NUM_PEAK: 25
PK$PEAK: m/z int. rel.int.
  216.89 88.3 1
  259.07 6022.3 70
  259.84 424.6 5
  260.44 215.4 3
  267.38 176.6 2
  282.96 217.3 3
  284.49 678.0 8
  285.28 298.5 3
  286.23 128.0 1
  287.29 51.9 1
  301.17 355.6 4
  303.04 85544.0 999
  304.05 6275.5 73
  304.66 213.1 2
  331.20 75.4 1
  404.04 111.8 1
  436.27 61.1 1
  439.15 182.7 2
  445.53 120.4 1
  446.16 4656.5 54
  447.21 310.5 4
  464.21 33317.3 389
  465.36 2897.7 34
  482.15 249.2 3
  595.90 117.8 1
//

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