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MassBank Record: MSBNK-Chubu_Univ-UT002590

Phosphatidylethanolamine 17:1-22:6; LC-ESI-ITFT; MS2; [M-H]-; RT: 13.99; Exp: 3

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

ACCESSION: MSBNK-Chubu_Univ-UT002590
RECORD_TITLE: Phosphatidylethanolamine 17:1-22:6; LC-ESI-ITFT; MS2; [M-H]-; RT: 13.99; 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$NAME: Phosphatidylethanolamine 17:1-22:6
CH$COMPOUND_CLASS: Natural Product; Glycerophospholipids; Glycerophosphoethanolamines; Diacylglycerophosphoethanolamines
CH$FORMULA: C44H74NO8P
CH$EXACT_MASS: 775.51520
CH$SMILES: C(CC)=CCC=CCC=CCC=CCC=CCC=CCCC(OC(COC(CCC=CCCCCCCCCCCCC)=O)COP(O)(=O)OCCN)=O
CH$IUPAC: InChI=1S/C44H74NO8P/c1-3-5-7-9-11-13-15-17-19-20-21-22-23-25-27-29-31-33-35-37-44(47)53-42(41-52-54(48,49)51-39-38-45)40-50-43(46)36-34-32-30-28-26-24-18-16-14-12-10-8-6-4-2/h5,7,11,13,17,19,21-22,25,27,30-33,42H,3-4,6,8-10,12,14-16,18,20,23-24,26,28-29,34-41,45H2,1-2H3,(H,48,49)/b7-5-,13-11-,19-17-,22-21-,27-25-,32-30-,33-31-
CH$LINK: INCHIKEY PKKFLKWXJRZTFJ-YZIPONAMSA-N
SP$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$CHROMATOGRAPHY: RETENTION_TIME 14.27 min (in paper: 14 min)
AC$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$FOCUSED_ION: PRECURSOR_M/Z 774.51
MS$FOCUSED_ION: PRECURSOR_TYPE [M-H]-
MS$DATA_PROCESSING: WHOLE Xcalibur ver-2.0

PK$SPLASH: splash10-00or-0096300000-f364a45182a03fb52006
PK$ANNOTATION: m/z num type mass error(ppm) formula
  267.09 1 [fa(17:1)-H]- 267.2324052393 -532 C17H31O2-
  283.17 1 [fa(22:6)-H-CO2]- 283.2425759951 -255 C21H31-
  327.10 1 [fa(22:6)-H]- 327.2324052393 -404 C22H31O2-
  464.02 1 [lyso_PE(17:1,-)]- 464.2777142502 -554 C22H43NO7P-
  524.07 1 [lyso_PE(-,22:6)]- 524.2777142502 -395 C27H43NO7P-
PK$NUM_PEAK: 17
PK$PEAK: m/z int. rel.int.
  229.08 37.7 97
  267.09 306.9 787
  268.40 24.7 63
  280.99 16.2 42
  283.17 171.3 439
  283.99 39.2 100
  327.10 389.7 999
  328.20 61.3 157
  403.26 12.9 33
  404.94 11.7 30
  447.34 12.9 33
  464.02 140.6 360
  465.12 34.1 87
  524.07 6.2 16
  627.28 22.7 58
  638.28 16.2 42
  700.15 18.5 47
//

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