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MassBank Record: MSBNK-Chubu_Univ-UT002902

Phosphatidylethanolamine alkenyl 18:1-22:2; LC-ESI-ITFT; MS2; [M-H]-; RT: 37.16; Exp: 3

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

ACCESSION: MSBNK-Chubu_Univ-UT002902
RECORD_TITLE: Phosphatidylethanolamine alkenyl 18:1-22:2; LC-ESI-ITFT; MS2; [M-H]-; RT: 37.16; 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$NAME: Phosphatidylethanolamine alkenyl 18:1-22:2
CH$COMPOUND_CLASS: Natural Product; Glycerophospholipids; Glycerophosphoethanolamines; 1Z-alkenyl,2-acylglycerophosphoethanolamines
CH$FORMULA: C45H84NO7P
CH$EXACT_MASS: 781.59854
CH$SMILES: NCCOP(OCC(COC=CCC=CCCCCCCCCCCCCC)OC(CCC=CCC=CCCCCCCCCCCCCCC)=O)(O)=O
CH$IUPAC: InChI=1S/C45H84NO7P/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/h26,28,31-34,37,40,44H,3-25,27,29-30,35-36,38-39,41-43,46H2,1-2H3,(H,48,49)/b28-26-,33-31-,34-32-,40-37+
CH$LINK: INCHIKEY AINWEGSZBADWKE-CFOOOPRVSA-N
SP$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$CHROMATOGRAPHY: RETENTION_TIME 37.00 min (in paper: 37.2 min)
AC$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$FOCUSED_ION: PRECURSOR_M/Z 780.59
MS$FOCUSED_ION: PRECURSOR_TYPE [M-H]-
MS$DATA_PROCESSING: WHOLE Xcalibur ver-2.0

PK$SPLASH: splash10-000i-0009100000-29c85ca33e1490f4325c
PK$ANNOTATION: m/z num type mass error(ppm) formula
  335.12 1 [fa(22:2)-H]- 335.2950054961 -521 C22H39O2-
  444.03 1 [lyso_PE(alkenyl-18:1,-)-H2O]- 444.287885006 -579 C23H43NO5P-
  462.19 1 [lyso_PE(alkenyl-18:1,-)]- 462.2984496923 -234 C23H45NO6P-
  488.14 1 [lyso_PE(-,22:2)-CO2]- 488.3504852628 -430 C26H51NO5P-
PK$NUM_PEAK: 31
PK$PEAK: m/z int. rel.int.
  282.71 9.9 4
  286.67 14.6 5
  287.46 7.0 2
  307.36 23.4 8
  308.14 16.2 6
  309.22 130.3 46
  310.20 25.9 9
  331.10 132.2 47
  332.09 133.0 47
  333.25 42.8 15
  335.12 2817.2 999
  336.03 400.3 142
  336.68 2.5 1
  339.48 3.1 1
  359.34 7.0 2
  444.03 54.6 19
  445.01 14.7 5
  462.19 494.5 175
  463.25 97.1 34
  464.35 14.5 5
  465.34 53.3 19
  466.30 23.3 8
  470.88 10.5 4
  474.25 7.6 3
  488.14 11.8 4
  491.09 9.8 3
  616.15 5.9 2
  618.50 22.3 8
  699.04 8.2 3
  719.94 25.2 9
  780.96 21.6 8
//

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