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MassBank Record: MSBNK-Chubu_Univ-UT002161

Phosphatidylethanolamine alkenyl 18:0-20:4; LC-ESI-ITFT; MS2; [M-H]-; RT: 30.78; Exp: 2

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

ACCESSION: MSBNK-Chubu_Univ-UT002161
RECORD_TITLE: Phosphatidylethanolamine alkenyl 18:0-20:4; LC-ESI-ITFT; MS2; [M-H]-; RT: 30.78; 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. 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$CHROMATOGRAPHY: RETENTION_TIME 30.57 min (in paper: 30.5 min)
AC$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$SPLASH: splash10-0udi-0009400000-b11de9060580928337a6
PK$ANNOTATION: m/z num type mass error(ppm) formula
  259.05 1 [fa(20:4)-H-CO2]- 259.2425759951 -742 C19H31-
  267.31 1 [fa(alkenyl-18:0)-H]- 267.2687907456 154 C18H35O-
  303.14 1 [fa(20:4)-H]- 303.2324052393 -304 C20H31O2-
  446.20 1 [lyso_PE(alkenyl-18:0,-)-H2O]- 446.3035350702 -231 C23H45NO5P-
  464.17 1 [lyso_PE(alkenyl-18:0,-)]- 464.3140997565 -309 C23H47NO6P-
PK$NUM_PEAK: 27
PK$PEAK: m/z int. rel.int.
  216.77 20.4 3
  233.00 9.4 1
  255.17 39.1 6
  256.20 9.9 1
  259.05 489.9 71
  260.04 37.7 5
  267.31 20.1 3
  283.21 82.8 12
  284.18 10.0 1
  285.23 33.9 5
  291.91 8.2 1
  303.14 6901.7 999
  304.17 543.7 79
  331.12 99.2 14
  332.25 9.6 1
  403.20 17.8 3
  404.37 5.4 1
  418.87 11.2 2
  437.61 8.2 1
  446.20 413.1 60
  447.14 46.8 7
  461.90 4.9 1
  464.17 3150.1 456
  465.26 374.6 54
  481.88 20.0 3
  600.42 16.6 2
  708.25 7.7 1
//

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