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MassBank Record: MSBNK-Chubu_Univ-UT002903

Phosphatidylethanolamine alkenyl 18:1-22:4; LC-ESI-ITFT; MS2; [M-H]-; RT: 26.41; Exp: 3

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

ACCESSION: MSBNK-Chubu_Univ-UT002903
RECORD_TITLE: Phosphatidylethanolamine alkenyl 18:1-22:4; LC-ESI-ITFT; MS2; [M-H]-; RT: 26.41; 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$NAME: Phosphatidylethanolamine alkenyl 18:1-22:4
CH$COMPOUND_CLASS: Natural Product; Glycerophospholipids; Glycerophosphoethanolamines; 1Z-alkenyl,2-acylglycerophosphoethanolamines
CH$FORMULA: C45H80NO7P
CH$EXACT_MASS: 777.56724
CH$SMILES: O(C(COC=CCC=CCCCCCCCCCCCCC)COP(O)(=O)OCCN)C(=O)CCC=CCC=CCC=CCC=CCCCCCCCC
CH$IUPAC: InChI=1S/C45H80NO7P/c1-3-5-7-9-11-13-15-17-19-21-22-23-24-26-28-30-32-34-36-38-45(47)53-44(43-52-54(48,49)51-41-39-46)42-50-40-37-35-33-31-29-27-25-20-18-16-14-12-10-8-6-4-2/h17,19,22-23,26,28,31-34,37,40,44H,3-16,18,20-21,24-25,27,29-30,35-36,38-39,41-43,46H2,1-2H3,(H,48,49)/b19-17-,23-22-,28-26-,33-31-,34-32-,40-37+
CH$LINK: INCHIKEY LLGDMLIODPBDGJ-IVEVXDSTSA-N
SP$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$CHROMATOGRAPHY: RETENTION_TIME 26.41 min (in paper: 26.4 min)
AC$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$FOCUSED_ION: PRECURSOR_M/Z 776.56
MS$FOCUSED_ION: PRECURSOR_TYPE [M-H]-
MS$DATA_PROCESSING: WHOLE Xcalibur ver-2.0

PK$SPLASH: splash10-001i-0009200000-ff113a25d86e29fbf6e4
PK$ANNOTATION: m/z num type mass error(ppm) formula
  265.04 1 [fa(alkenyl-18:1)-H]- 265.2531406814 -803 C18H33O-
  287.16 1 [fa(22:4)-H-CO2]- 287.2738761235 -395 C21H35-
  331.13 1 [fa(22:4)-H]- 331.2637053677 -403 C22H35O2-
  444.24 1 [lyso_PE(alkenyl-18:1,-)-H2O]- 444.287885006 -107 C23H43NO5P-
  462.06 1 [lyso_PE(alkenyl-18:1,-)]- 462.2984496923 -515 C23H45NO6P-
  510.03 1 [lyso_PE(-,22:4)-H2O]- 510.2984496923 -525 C27H45NO6P-
PK$NUM_PEAK: 23
PK$PEAK: m/z int. rel.int.
  233.16 234.5 6
  265.04 114.6 3
  287.16 1383.0 37
  288.22 201.4 5
  311.21 15.5 1
  313.12 66.7 2
  328.20 21.9 1
  329.07 80.5 2
  331.13 37200.3 999
  332.21 4131.7 111
  401.04 234.1 6
  402.20 57.5 2
  443.63 41.0 1
  444.24 1269.3 34
  445.19 242.8 7
  462.06 9193.4 247
  463.10 1830.5 49
  463.90 23.2 1
  510.03 40.5 1
  694.42 44.3 1
  702.61 12.4 1
  715.68 30.4 1
  717.30 21.9 1
//

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