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MassBank Record: MSBNK-Chubu_Univ-UT002623

Phosphatidylethanolamine 20:0-20:3; LC-ESI-ITFT; MS2; [M-H]-; RT: 39.26; Exp: 3

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

ACCESSION: MSBNK-Chubu_Univ-UT002623
RECORD_TITLE: Phosphatidylethanolamine 20:0-20:3; LC-ESI-ITFT; MS2; [M-H]-; RT: 39.26; 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$NAME: Phosphatidylethanolamine 20:0-20:3
CH$COMPOUND_CLASS: Natural Product; Glycerophospholipids; Glycerophosphoethanolamines; Diacylglycerophosphoethanolamines
CH$FORMULA: C45H84NO8P
CH$EXACT_MASS: 797.59346
CH$SMILES: C(COP(OCCN)(O)=O)(COC(CCCCCCCCCCCCCCCCCCC)=O)OC(=O)CCC=CCC=CCC=CCCCCCCCCC
CH$IUPAC: InChI=1S/C45H84NO8P/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-35-37-44(47)51-41-43(42-53-55(49,50)52-40-39-46)54-45(48)38-36-34-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h20,22,26,28,32,34,43H,3-19,21,23-25,27,29-31,33,35-42,46H2,1-2H3,(H,49,50)/b22-20-,28-26-,34-32-
CH$LINK: INCHIKEY FJLSFWWSNVGVIN-KWKIUDPJSA-N
SP$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: liver

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$CHROMATOGRAPHY: RETENTION_TIME 39.00 min (in paper: 39.3 min)
AC$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$FOCUSED_ION: PRECURSOR_M/Z 796.59
MS$FOCUSED_ION: PRECURSOR_TYPE [M-H]-
MS$DATA_PROCESSING: WHOLE Xcalibur ver-2.0

PK$SPLASH: splash10-0a4i-0009010100-2839ec10e417ebd517b0
PK$ANNOTATION: m/z num type mass error(ppm) formula
  305.01 1 [fa(20:3)-H]- 305.2480553035 -779 C20H33O2-
  311.10 1 [fa(20:0)-H]- 311.2950054961 -625 C20H39O2-
  484.34 1 [lyso_PE(-,20:3)-H2O]- 484.2827996281 118 C25H43NO6P-
  490.27 1 [lyso_PE(20:0,-)-H2O]- 490.3297498207 -121 C25H49NO6P-
  752.78 1 [PE(20:0,20:3)-H-CO2]- 752.5958009121 245 C44H83NO6P-
PK$NUM_PEAK: 18
PK$PEAK: m/z int. rel.int.
  305.01 357.2 999
  306.02 57.8 162
  311.10 119.9 335
  312.17 31.9 89
  484.34 13.9 39
  490.27 10.5 29
  507.96 53.7 150
  567.67 12.2 34
  709.02 9.5 27
  731.72 16.0 45
  735.54 25.8 72
  736.31 16.5 46
  737.47 8.8 25
  739.04 5.4 15
  744.34 13.0 36
  751.53 12.9 36
  752.78 8.2 23
  763.55 6.5 18
//

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