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MassBank Record: MSBNK-Chubu_Univ-UT002960

Phosphatidylserine 18:0-20:1; LC-ESI-ITFT; MS2; [M-H]-; RT: 43.92; Exp: 3

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

ACCESSION: MSBNK-Chubu_Univ-UT002960
RECORD_TITLE: Phosphatidylserine 18:0-20:1; LC-ESI-ITFT; MS2; [M-H]-; RT: 43.92; Exp: 3
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$NAME: Phosphatidylserine 18:0-20:1
CH$COMPOUND_CLASS: Natural Product; Glycerophospholipids; Glycerophosphoserines; Diacylglycerophosphoserines
CH$FORMULA: C44H84NO10P
CH$EXACT_MASS: 817.58328
CH$SMILES: C(CCCCCCC)CCCCCCCCCC(=O)OCC(COP(OCC(C(O)=O)N)(O)=O)OC(=O)CCC=CCCCCCCCCCCCCCCC
CH$IUPAC: InChI=1S/C44H84NO10P/c1-3-5-7-9-11-13-15-17-19-20-22-24-26-28-30-32-34-36-43(47)55-40(38-53-56(50,51)54-39-41(45)44(48)49)37-52-42(46)35-33-31-29-27-25-23-21-18-16-14-12-10-8-6-4-2/h30,32,40-41H,3-29,31,33-39,45H2,1-2H3,(H,48,49)(H,50,51)/b32-30-
CH$LINK: INCHIKEY CWSHAMZVMDYRSO-GCUVURNUSA-N
SP$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$CHROMATOGRAPHY: RETENTION_TIME 44.00 min (in paper: 43.9 min)
AC$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$FOCUSED_ION: PRECURSOR_M/Z 816.58
MS$FOCUSED_ION: PRECURSOR_TYPE [M-H]-
MS$DATA_PROCESSING: WHOLE Xcalibur ver-2.0

PK$SPLASH: splash10-004i-0000100900-0f04898378757e53797b
PK$ANNOTATION: m/z num type mass error(ppm) formula
  281.27 1 [fa(18:1)-H]- 281.2480553035 78 C18H33O2-
  309.15 1 [fa(20:1)-H]- 309.2793554319 -417 C20H37O2-
  311.56 1 [fa(20:0)-H]- 311.2950054961 851 C20H39O2-
  417.05 1 [lyso_PS(18:1,-)-H2O]- 417.2406004624 -456 C21H38O6P-
  419.05 2 [lyso_PS(-,20:1)-CO2]- 419.2926360329 -578 C22H44O5P-
  419.05 2 [lyso_PS(18:0,-)-H2O]- 419.2562505266 -491 C21H40O6P-
  437.18 1 [lyso_PS(18:0,-)]- 437.2668152129 -198 C21H42O7P-
  445.09 1 [lyso_PS(-,20:1)-H2O]- 445.2719005908 -408 C23H42O6P-
  447.19 1 [lyso_PS(-,20:0)-H2O]- 447.287550655 -217 C23H44O6P-
  463.26 1 [lyso_PS(-,20:1)]- 463.2824652771 -47 C23H44O7P-
PK$NUM_PEAK: 31
PK$PEAK: m/z int. rel.int.
  281.27 30.2 7
  282.94 151.2 33
  284.25 23.0 5
  309.15 127.2 27
  309.84 12.9 3
  310.64 13.4 3
  311.56 16.9 4
  312.22 7.8 2
  417.05 70.4 15
  417.87 10.0 2
  419.05 486.5 105
  420.15 169.1 36
  437.18 111.3 24
  445.09 216.4 47
  447.19 136.6 29
  448.19 34.6 7
  463.26 8.9 2
  466.29 11.7 3
  522.11 11.2 2
  628.78 13.4 3
  630.62 17.4 4
  729.10 4637.2 999
  730.09 1548.8 334
  730.78 19.0 4
  742.20 32.6 7
  755.02 8.4 2
  756.26 5.6 1
  773.68 12.9 3
  777.95 15.1 3
  780.87 6.1 1
  817.95 9.5 2
//

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