MassBank MassBank Search Contents Download

MassBank Record: MSBNK-Chubu_Univ-UT002245

Phosphatidylserine 18:1-22:6; LC-ESI-ITFT; MS2; [M-H]-; RT: 15.16; Exp: 2

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

ACCESSION: MSBNK-Chubu_Univ-UT002245
RECORD_TITLE: Phosphatidylserine 18:1-22:6; LC-ESI-ITFT; MS2; [M-H]-; RT: 15.16; Exp: 2
DATE: 2016.01.19 (Created 2010.05.07, modified 2013.05.16)
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$NAME: Phosphatidylserine 18:1-22:6
CH$COMPOUND_CLASS: Natural Product; Glycerophospholipids; Glycerophosphoserines; Diacylglycerophosphoserines
CH$FORMULA: C46H76NO10P
CH$EXACT_MASS: 833.52068
CH$SMILES: C(CCCCCCCCC=CCCC(=O)OCC(COP(O)(=O)OCC(N)C(O)=O)OC(CCC=CCC=CCC=CCC=CCC=CCC=CCC)=O)CCCC
CH$IUPAC: InChI=1S/C46H76NO10P/c1-3-5-7-9-11-13-15-17-19-20-21-22-24-26-28-30-32-34-36-38-45(49)57-42(40-55-58(52,53)56-41-43(47)46(50)51)39-54-44(48)37-35-33-31-29-27-25-23-18-16-14-12-10-8-6-4-2/h5,7,11,13,17,19,21-22,26,28,31-34,42-43H,3-4,6,8-10,12,14-16,18,20,23-25,27,29-30,35-41,47H2,1-2H3,(H,50,51)(H,52,53)/b7-5-,13-11-,19-17-,22-21-,28-26-,33-31-,34-32-
CH$LINK: INCHIKEY ZBHJZQBBODCTLM-QRPORDCISA-N
SP$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$CHROMATOGRAPHY: RETENTION_TIME 15.33 min (in paper: 15.2 min)
AC$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$FOCUSED_ION: PRECURSOR_M/Z 832.51
MS$FOCUSED_ION: PRECURSOR_TYPE [M-H]-
MS$DATA_PROCESSING: WHOLE Xcalibur ver-2.0

PK$SPLASH: splash10-0006-0000100900-7e13bd08f809523cc425
PK$ANNOTATION: m/z num type mass error(ppm) formula
  281.20 1 [fa(18:1)-H]- 281.2480553035 -170 C18H33O2-
  283.17 1 [fa(22:6)-H-CO2]- 283.2425759951 -255 C21H31-
  327.07 1 [fa(22:6)-H]- 327.2324052393 -495 C22H31O2-
  417.00 1 [lyso_PS(18:1,-)-H2O]- 417.2406004624 -576 C21H38O6P-
  435.19 1 [lyso_PS(18:1,-)]- 435.2511651487 -140 C21H40O7P-
  462.99 1 [lyso_PS(-,22:6)-H2O]- 463.2249503982 -506 C25H36O6P-
PK$NUM_PEAK: 20
PK$PEAK: m/z int. rel.int.
  281.20 191.5 51
  282.32 39.6 11
  283.17 14.5 4
  297.04 57.2 15
  327.07 23.5 6
  417.00 557.6 150
  418.20 60.5 16
  435.19 105.3 28
  462.99 130.9 35
  463.79 27.2 7
  522.00 26.0 7
  551.43 7.2 2
  553.10 209.7 56
  571.23 6.2 2
  576.91 199.7 54
  577.75 17.9 5
  744.99 3717.5 999
  746.18 710.0 191
  750.62 8.8 2
  758.10 24.3 7
//

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