MassBank MassBank Search Contents Download

MassBank Record: MSBNK-Chubu_Univ-UT001863

Phosphatidylethanolamine 18:0-18:3; LC-ESI-ITFT; MS2; [M-H]-; RT: 24.54; Exp: 2

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

ACCESSION: MSBNK-Chubu_Univ-UT001863
RECORD_TITLE: Phosphatidylethanolamine 18:0-18:3; LC-ESI-ITFT; MS2; [M-H]-; RT: 24.54; 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$NAME: Phosphatidylethanolamine 18:0-18:3
CH$COMPOUND_CLASS: Natural Product; Glycerophospholipids; Glycerophosphoethanolamines; Diacylglycerophosphoethanolamines
CH$FORMULA: C41H76NO8P
CH$EXACT_MASS: 741.53085
CH$SMILES: C(CCCCCCCCCCCCCC)CCC(OCC(OC(CCC=CCC=CCC=CCCCCCCC)=O)COP(O)(=O)OCCN)=O
CH$IUPAC: InChI=1S/C41H76NO8P/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-40(43)47-37-39(38-49-51(45,46)48-36-35-42)50-41(44)34-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h16,18,22,24,28,30,39H,3-15,17,19-21,23,25-27,29,31-38,42H2,1-2H3,(H,45,46)/b18-16-,24-22-,30-28-
CH$LINK: INCHIKEY LXDJYUCSACQJRW-FQQNHZGCSA-N
SP$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$CHROMATOGRAPHY: RETENTION_TIME 24.48 min (in paper: 24.5 min)
AC$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$FOCUSED_ION: PRECURSOR_M/Z 740.52
MS$FOCUSED_ION: PRECURSOR_TYPE [M-H]-
MS$DATA_PROCESSING: WHOLE Xcalibur ver-2.0

PK$SPLASH: splash10-0059-0091100000-7d11d9aa63cdc496c2a1
PK$ANNOTATION: m/z num type mass error(ppm) formula
  233.13 1 [fa(18:3)-H-CO2]- 233.2269259309 -415 C17H29-
  277.12 1 [fa(18:3)-H]- 277.2167551751 -348 C18H29O2-
  283.19 1 [fa(18:0)-H]- 283.2637053677 -259 C18H35O2-
  474.34 1 [lyso_PE(-,18:3)]- 474.262064186 164 C23H41NO7P-
  480.27 1 [lyso_PE(18:0,-)]- 480.3090143786 -80 C23H47NO7P-
PK$NUM_PEAK: 22
PK$PEAK: m/z int. rel.int.
  233.13 10.4 12
  255.03 96.2 112
  256.08 16.4 19
  259.07 7.0 8
  277.12 856.0 999
  278.14 92.6 108
  279.17 42.1 49
  281.27 4.5 5
  283.19 414.7 484
  284.27 26.3 31
  304.99 187.4 219
  305.98 26.2 31
  452.07 18.8 22
  453.33 20.6 24
  474.34 11.9 14
  477.94 18.2 21
  480.27 221.5 259
  481.15 10.8 13
  503.09 7.3 9
  600.61 9.3 11
  679.24 5.8 7
  681.56 11.1 13
//

system version 2.2.6-SNAPSHOT
Copyright © 2006 MassBank Project; 2011 NORMAN Association; 2021 MassBank Consortium
de.NBI logo
EAWAG logo
fnr logo
IPB logo
NORMAN logo
UFZ logo
LCSB logo
HBM4EU logo
nfdi4chem logo