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MassBank Record: MSBNK-Chubu_Univ-UT001918

Phosphatidylethanolamine alkenyl 18:1-22:4; LC-ESI-ITFT; MS2; [M-H]-; RT: 26.35; Exp: 2

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

ACCESSION: MSBNK-Chubu_Univ-UT001918
RECORD_TITLE: Phosphatidylethanolamine alkenyl 18:1-22:4; LC-ESI-ITFT; MS2; [M-H]-; RT: 26.35; 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$NAME: Phosphatidylethanolamine alkenyl 18:1-22:4
CH$COMPOUND_CLASS: Natural Product; Glycerophospholipids; Glycerophosphoethanolamines; 1Z-alkenyl,2-acylglycerophosphoethanolamines
CH$FORMULA: C45H80NO7P
CH$EXACT_MASS: 777.56724
CH$SMILES: O(C(COC=CCC=CCCCCCCCCCCCCC)COP(O)(=O)OCCN)C(=O)CCC=CCC=CCC=CCC=CCCCCCCCC
CH$IUPAC: InChI=1S/C45H80NO7P/c1-3-5-7-9-11-13-15-17-19-21-22-23-24-26-28-30-32-34-36-38-45(47)53-44(43-52-54(48,49)51-41-39-46)42-50-40-37-35-33-31-29-27-25-20-18-16-14-12-10-8-6-4-2/h17,19,22-23,26,28,31-34,37,40,44H,3-16,18,20-21,24-25,27,29-30,35-36,38-39,41-43,46H2,1-2H3,(H,48,49)/b19-17-,23-22-,28-26-,33-31-,34-32-,40-37+
CH$LINK: INCHIKEY LLGDMLIODPBDGJ-IVEVXDSTSA-N
SP$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$CHROMATOGRAPHY: RETENTION_TIME 26.24 min (in paper: 26.4 min)
AC$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$FOCUSED_ION: PRECURSOR_M/Z 776.56
MS$FOCUSED_ION: PRECURSOR_TYPE [M-H]-
MS$DATA_PROCESSING: WHOLE Xcalibur ver-2.0

PK$SPLASH: splash10-001i-0019200200-024fab181f45aaf166ed
PK$ANNOTATION: m/z num type mass error(ppm) formula
  265.20 1 [fa(alkenyl-18:1)-H]- 265.2531406814 -199 C18H33O-
  287.19 1 [fa(22:4)-H-CO2]- 287.2738761235 -291 C21H35-
  331.24 1 [fa(22:4)-H]- 331.2637053677 -71 C22H35O2-
  444.12 1 [lyso_PE(alkenyl-18:1,-)-H2O]- 444.287885006 -377 C23H43NO5P-
  462.29 1 [lyso_PE(alkenyl-18:1,-)]- 462.2984496923 -17 C23H45NO6P-
PK$NUM_PEAK: 22
PK$PEAK: m/z int. rel.int.
  233.05 7.5 10
  233.94 5.4 8
  265.20 14.4 20
  269.29 8.7 12
  281.13 5.3 7
  287.19 46.5 65
  288.54 10.4 15
  331.24 714.2 999
  332.31 131.9 184
  333.42 6.6 9
  444.12 35.1 49
  452.70 4.8 7
  461.32 12.1 17
  462.29 204.9 287
  463.28 18.9 26
  509.94 12.7 18
  693.31 10.4 15
  694.94 5.4 8
  702.10 148.2 207
  712.69 14.3 20
  716.35 57.6 81
  717.58 13.2 18
//

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