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MassBank Record: MSBNK-Chubu_Univ-UT002120

Phosphatidylethanolamine 18:0-22:1; LC-ESI-ITFT; MS2; [M-H]-; RT: 45.88; Exp: 2

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

ACCESSION: MSBNK-Chubu_Univ-UT002120
RECORD_TITLE: Phosphatidylethanolamine 18:0-22:1; LC-ESI-ITFT; MS2; [M-H]-; RT: 45.88; 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$NAME: Phosphatidylethanolamine 18:0-22:1
CH$COMPOUND_CLASS: Natural Product; Glycerophospholipids; Glycerophosphoethanolamines; Diacylglycerophosphoethanolamines
CH$FORMULA: C45H88NO8P
CH$EXACT_MASS: 801.62476
CH$SMILES: C(CC=CCCCCCCCCCCCCCCCCC)C(=O)OC(COC(CCCCCCCCCCCCCCCCC)=O)COP(OCCN)(O)=O
CH$IUPAC: InChI=1S/C45H88NO8P/c1-3-5-7-9-11-13-15-17-19-20-21-22-24-26-28-30-32-34-36-38-45(48)54-43(42-53-55(49,50)52-40-39-46)41-51-44(47)37-35-33-31-29-27-25-23-18-16-14-12-10-8-6-4-2/h32,34,43H,3-31,33,35-42,46H2,1-2H3,(H,49,50)/b34-32-
CH$LINK: INCHIKEY HHIOTAKOFGPHDM-YJKCNMNRSA-N
SP$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$CHROMATOGRAPHY: RETENTION_TIME 45.87 min (in paper: 45.9 min)
AC$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$FOCUSED_ION: PRECURSOR_M/Z 800.62
MS$FOCUSED_ION: PRECURSOR_TYPE [M-H]-
MS$DATA_PROCESSING: WHOLE Xcalibur ver-2.0

PK$SPLASH: splash10-000i-0019000000-eec70565399b74247725
PK$ANNOTATION: m/z num type mass error(ppm) formula
  283.19 1 [fa(18:0)-H]- 283.2637053677 -259 C18H35O2-
  337.19 1 [fa(22:1)-H]- 337.3106555603 -357 C22H41O2-
  480.06 1 [lyso_PE(18:0,-)]- 480.3090143786 -517 C23H47NO7P-
  756.84 1 [PE(18:0,22:1)-H-CO2]- 756.6271010405 281 C44H87NO6P-
PK$NUM_PEAK: 27
PK$PEAK: m/z int. rel.int.
  283.19 131.2 142
  284.02 15.2 16
  284.74 13.8 15
  309.12 102.6 111
  311.18 37.5 40
  337.19 925.3 999
  338.24 130.6 141
  365.18 22.5 24
  480.06 57.2 62
  481.03 22.7 25
  507.90 12.6 14
  533.76 7.9 9
  534.83 16.6 18
  620.06 7.4 8
  620.73 27.6 30
  635.74 10.1 11
  636.37 6.2 7
  707.28 7.8 8
  714.44 8.4 9
  717.25 12.4 13
  717.87 9.5 10
  718.66 17.7 19
  739.88 20.3 22
  746.84 12.4 13
  756.84 5.0 5
  781.41 9.0 10
  784.70 11.8 13
//

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