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MassBank Record: MSBNK-Chubu_Univ-UT001386

Phosphatidylethanolamine 18:1-20:4; LC-ESI-ITFT; MS2; [M-H]-; RT: 18.53; Exp: 1

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

ACCESSION: MSBNK-Chubu_Univ-UT001386
RECORD_TITLE: Phosphatidylethanolamine 18:1-20:4; LC-ESI-ITFT; MS2; [M-H]-; RT: 18.53; Exp: 1
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$NAME: Phosphatidylethanolamine 18:1-20:4
CH$COMPOUND_CLASS: Natural Product; Glycerophospholipids; Glycerophosphoethanolamines; Diacylglycerophosphoethanolamines
CH$FORMULA: C43H76NO8P
CH$EXACT_MASS: 765.53085
CH$SMILES: O(CCN)P(O)(=O)OCC(OC(=O)CCC=CCC=CCC=CCC=CCCCCCC)COC(CCC=CCCCCCCCCCCCCC)=O
CH$IUPAC: InChI=1S/C43H76NO8P/c1-3-5-7-9-11-13-15-17-19-20-22-24-26-28-30-32-34-36-43(46)52-41(40-51-53(47,48)50-38-37-44)39-49-42(45)35-33-31-29-27-25-23-21-18-16-14-12-10-8-6-4-2/h13,15,19-20,24,26,29-32,41H,3-12,14,16-18,21-23,25,27-28,33-40,44H2,1-2H3,(H,47,48)/b15-13-,20-19-,26-24-,31-29-,32-30-
CH$LINK: INCHIKEY QBVUKWXEFSHJOQ-MOYSMJPMSA-N
SP$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$CHROMATOGRAPHY: RETENTION_TIME 18.61 min (in paper: 18.6 min)
AC$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$FOCUSED_ION: PRECURSOR_M/Z 764.52
MS$FOCUSED_ION: PRECURSOR_TYPE [M-H]-
MS$DATA_PROCESSING: WHOLE Xcalibur ver-2.0

PK$SPLASH: splash10-0udi-0049200000-c9ef8f8c1047b97ca1b6
PK$ANNOTATION: m/z num type mass error(ppm) formula
  259.15 1 [fa(20:4)-H-CO2]- 259.2425759951 -356 C19H31-
  281.22 1 [fa(18:1)-H]- 281.2480553035 -99 C18H33O2-
  303.04 1 [fa(20:4)-H]- 303.2324052393 -634 C20H31O2-
  460.10 1 [lyso_PE(18:1,-)-H2O]- 460.2827996281 -396 C23H43NO6P-
  478.11 1 [lyso_PE(18:1,-)]- 478.2933643144 -382 C23H45NO7P-
  500.15 1 [lyso_PE(-,20:4)]- 500.2777142502 -254 C25H43NO7P-
PK$NUM_PEAK: 19
PK$PEAK: m/z int. rel.int.
  255.20 12.5 1
  256.99 17.5 1
  259.15 2028.2 78
  259.97 85.0 3
  281.22 12935.9 496
  282.19 472.3 18
  284.41 36.8 1
  301.00 60.8 2
  303.04 26054.2 999
  304.14 1959.8 75
  327.31 20.6 1
  328.07 25.4 1
  362.80 35.2 1
  426.03 19.0 1
  460.10 459.9 18
  478.11 6658.7 255
  479.12 279.3 11
  481.91 221.3 8
  500.15 485.0 19
//

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