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MassBank Record: MSBNK-Chubu_Univ-UT003084

Phosphatidylserine 18:0-20:5; LC-ESI-ITFT; MS3; [M-H]-/[M-C3H6NO2]-; RT: 20.89; Exp: 3

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

ACCESSION: MSBNK-Chubu_Univ-UT003084
RECORD_TITLE: Phosphatidylserine 18:0-20:5; LC-ESI-ITFT; MS3; [M-H]-/[M-C3H6NO2]-; RT: 20.89; 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
COMMENT: PRECURSOR_TYPE [M-H]-/[M-Ser]-

CH$NAME: Phosphatidylserine 18:0-20:5
CH$COMPOUND_CLASS: Natural Product; Glycerophospholipids; Glycerophosphoserines; Diacylglycerophosphoserines
CH$FORMULA: C45H78NO9P
CH$EXACT_MASS: 807.54142
CH$SMILES: C(N)(C(C)=O)COP(O)(=O)OCC(COC(CCCCCCCCCCCCCCCCC)=O)OC(CCC=CCC=CCC=CCC=CCC=CCCC)=O
CH$IUPAC: InChI=1S/C45H78NO9P/c1-4-6-8-10-12-14-16-18-20-21-23-25-27-29-31-33-35-37-45(49)55-42(39-53-56(50,51)54-40-43(46)41(3)47)38-52-44(48)36-34-32-30-28-26-24-22-19-17-15-13-11-9-7-5-2/h8,10,14,16,20-21,25,27,31,33,42-43H,4-7,9,11-13,15,17-19,22-24,26,28-30,32,34-40,46H2,1-3H3,(H,50,51)/b10-8-,16-14-,21-20-,27-25-,33-31-
CH$LINK: INCHIKEY APKRXSJWVBFXCI-SQEBLUTFSA-N
SP$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$MASS_SPECTROMETRY: MS_TYPE MS3
AC$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$CHROMATOGRAPHY: RETENTION_TIME 21.24 min (in paper: 20.9 min)
AC$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$FOCUSED_ION: PRECURSOR_M/Z 808.51/721.07
MS$FOCUSED_ION: PRECURSOR_TYPE [M-H]-/[M-C3H6NO2]-
MS$DATA_PROCESSING: WHOLE Xcalibur ver-2.0

PK$SPLASH: splash10-015i-0040900000-e628a25b7b94884fd3c6
PK$ANNOTATION: m/z num type mass error(ppm) formula
  256.99 1 [fa(20:5)-H-CO2]- 257.2269259309 -920 C19H29-
  283.18 1 [fa(18:0)-H]- 283.2637053677 -295 C18H35O2-
  301.31 1 [fa(20:5)-H]- 301.2167551751 310 C20H29O2-
  419.50 1 [lyso_PS(18:0,-)-H2O]- 419.2562505266 581 C21H40O6P-
  437.05 2 [lyso_PS(-,20:5)-H2O]- 437.209300334 -363 C23H34O6P-
  437.05 2 [lyso_PS(18:0,-)]- 437.2668152129 -495 C21H42O7P-
PK$NUM_PEAK: 13
PK$PEAK: m/z int. rel.int.
  256.99 6.9 32
  281.48 11.9 55
  283.18 180.7 833
  301.31 11.4 53
  329.27 11.4 53
  392.07 9.1 42
  409.06 4.6 21
  416.99 17.3 80
  418.89 216.6 999
  419.50 18.1 83
  437.05 146.0 673
  438.68 5.2 24
  454.88 5.7 26
//

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