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MassBank Record: MSBNK-Chubu_Univ-UT001887

Phosphatidylethanolamine 19:0-20:4; LC-ESI-ITFT; MS2; [M-H]-; RT: 31.24; Exp: 2

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

ACCESSION: MSBNK-Chubu_Univ-UT001887
RECORD_TITLE: Phosphatidylethanolamine 19:0-20:4; LC-ESI-ITFT; MS2; [M-H]-; RT: 31.24; 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$NAME: Phosphatidylethanolamine 19:0-20:4
CH$COMPOUND_CLASS: Natural Product; Glycerophospholipids; Glycerophosphoethanolamines; Diacylglycerophosphoethanolamines
CH$FORMULA: C44H80NO8P
CH$EXACT_MASS: 781.56216
CH$SMILES: C(CCCCCC)=CCC=CCC=CCC=CCCC(=O)OC(COP(OCCN)(O)=O)COC(CCCCCCCCCCCCCCCCCC)=O
CH$IUPAC: InChI=1S/C44H80NO8P/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-35-37-44(47)53-42(41-52-54(48,49)51-39-38-45)40-50-43(46)36-34-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h13,15,19,21,25,27,31,33,42H,3-12,14,16-18,20,22-24,26,28-30,32,34-41,45H2,1-2H3,(H,48,49)/b15-13-,21-19-,27-25-,33-31-
CH$LINK: INCHIKEY GGEYNVXDNWJXIN-SLLFMANOSA-N
SP$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$CHROMATOGRAPHY: RETENTION_TIME 31.35 min (in paper: 31.2 min)
AC$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$FOCUSED_ION: PRECURSOR_M/Z 780.55
MS$FOCUSED_ION: PRECURSOR_TYPE [M-H]-
MS$DATA_PROCESSING: WHOLE Xcalibur ver-2.0

PK$SPLASH: splash10-0udi-0059200000-ba423c1c77c052189f71
PK$ANNOTATION: m/z num type mass error(ppm) formula
  259.10 1 [fa(20:4)-H-CO2]- 259.2425759951 -549 C19H31-
  297.11 1 [fa(19:0)-H]- 297.2793554319 -569 C19H37O2-
  303.02 1 [fa(20:4)-H]- 303.2324052393 -699 C20H31O2-
  476.18 1 [lyso_PE(19:0,-)-H2O]- 476.3140997565 -281 C24H47NO6P-
  482.41 1 [lyso_PE(-,20:4)-H2O]- 482.2671495639 296 C25H41NO6P-
  494.07 1 [lyso_PE(19:0,-)]- 494.3246644428 -514 C24H49NO7P-
  500.16 1 [lyso_PE(-,20:4)]- 500.2777142502 -234 C25H43NO7P-
PK$NUM_PEAK: 25
PK$PEAK: m/z int. rel.int.
  259.10 371.0 76
  260.23 41.5 9
  267.52 10.0 2
  270.35 8.5 2
  285.23 36.8 8
  297.11 2712.6 558
  298.24 337.2 69
  303.02 4860.7 999
  304.13 608.1 125
  476.18 47.9 10
  482.41 45.5 9
  494.07 1399.2 288
  495.06 183.8 38
  500.16 78.3 16
  500.95 6.8 1
  632.25 14.5 3
  674.45 5.7 1
  681.28 4.6 1
  698.54 20.6 4
  699.33 7.2 1
  705.86 18.8 4
  722.73 10.8 2
  730.17 39.5 8
  734.52 11.3 2
  736.17 8.3 2
//

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