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MassBank Record: MSBNK-Chubu_Univ-UT001879

Phosphatidylethanolamine 18:2-20:4; LC-ESI-ITFT; MS2; [M-H]-; RT: 13.66; Exp: 2

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

ACCESSION: MSBNK-Chubu_Univ-UT001879
RECORD_TITLE: Phosphatidylethanolamine 18:2-20:4; LC-ESI-ITFT; MS2; [M-H]-; RT: 13.66; 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$NAME: Phosphatidylethanolamine 18:2-20:4
CH$COMPOUND_CLASS: Natural Product; Glycerophospholipids; Glycerophosphoethanolamines; Diacylglycerophosphoethanolamines
CH$FORMULA: C43H74NO8P
CH$EXACT_MASS: 763.51520
CH$SMILES: C(CCCCCC)CCCC=CCC=CCCC(OCC(COP(OCCN)(O)=O)OC(=O)CCC=CCC=CCC=CCC=CCCCCCC)=O
CH$IUPAC: InChI=1S/C43H74NO8P/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/h13,15,19-20,23-26,29-32,41H,3-12,14,16-18,21-22,27-28,33-40,44H2,1-2H3,(H,47,48)/b15-13-,20-19-,25-23-,26-24-,31-29-,32-30-
CH$LINK: INCHIKEY VTQZPEHDNCIYJA-IPVVXUKZSA-N
SP$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$CHROMATOGRAPHY: RETENTION_TIME 13.83 min (in paper: 13.7 min)
AC$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$FOCUSED_ION: PRECURSOR_M/Z 762.51
MS$FOCUSED_ION: PRECURSOR_TYPE [M-H]-
MS$DATA_PROCESSING: WHOLE Xcalibur ver-2.0

PK$SPLASH: splash10-0ufr-0049200000-4237acecece7e01cfaa9
PK$ANNOTATION: m/z num type mass error(ppm) formula
  259.14 1 [fa(20:4)-H-CO2]- 259.2425759951 -395 C19H31-
  279.13 1 [fa(18:2)-H]- 279.2324052393 -366 C18H31O2-
  303.10 1 [fa(20:4)-H]- 303.2324052393 -436 C20H31O2-
  458.06 1 [lyso_PE(18:2,-)-H2O]- 458.2671495639 -451 C23H41NO6P-
  476.08 1 [lyso_PE(18:2,-)]- 476.2777142502 -414 C23H43NO7P-
  482.07 1 [lyso_PE(-,20:4)-H2O]- 482.2671495639 -408 C25H41NO6P-
  500.18 1 [lyso_PE(-,20:4)]- 500.2777142502 -194 C25H43NO7P-
PK$NUM_PEAK: 23
PK$PEAK: m/z int. rel.int.
  252.66 16.5 4
  259.14 165.9 45
  260.15 17.9 5
  279.13 1447.6 393
  280.17 193.3 52
  284.90 11.4 3
  301.01 25.8 7
  303.10 3679.5 999
  304.10 370.4 101
  315.05 5.2 1
  326.96 10.8 3
  399.32 6.9 2
  402.07 13.7 4
  452.27 14.0 4
  453.19 14.0 4
  458.06 51.7 14
  476.08 706.5 192
  477.23 123.9 34
  482.07 14.8 4
  500.18 29.5 8
  501.01 10.0 3
  687.86 91.4 25
  701.81 6.3 2
//

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