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MassBank Record: MSBNK-Chubu_Univ-UT001225

Phosphatidylinositol 16:0-20:4; LC-ESI-ITFT; MS2; [M-H]-; RT: 13.77; Exp: 1

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

ACCESSION: MSBNK-Chubu_Univ-UT001225
RECORD_TITLE: Phosphatidylinositol 16:0-20:4; LC-ESI-ITFT; MS2; [M-H]-; RT: 13.77; Exp: 1
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$NAME: Phosphatidylinositol 16:0-20:4
CH$COMPOUND_CLASS: Natural Product; Glycerophospholipids; Glycerophosphoinositols; Diacylglycerophosphoinositols
CH$FORMULA: C45H79O13P
CH$EXACT_MASS: 858.52583
CH$SMILES: C(CCCCCC)=CCC=CCC=CCC=CCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC)COP(O)(=O)OC(C(O)1)C(O)C(O)C(O)C(O)1
CH$IUPAC: InChI=1S/C45H79O13P/c1-3-5-7-9-11-13-15-17-18-19-20-22-24-26-28-30-32-34-39(47)57-37(36-56-59(53,54)58-45-43(51)41(49)40(48)42(50)44(45)52)35-55-38(46)33-31-29-27-25-23-21-16-14-12-10-8-6-4-2/h13,15,18-19,22,24,28,30,37,40-45,48-52H,3-12,14,16-17,20-21,23,25-27,29,31-36H2,1-2H3,(H,53,54)/b15-13-,19-18-,24-22-,30-28-/t37?,40-,41-,42+,43-,44-,45-/m1/s1
CH$LINK: INCHIKEY QAOYQEIOBPZFPB-VHZSRAIHSA-N
SP$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$CHROMATOGRAPHY: RETENTION_TIME 13.92 min (in paper: 13.8 min)
AC$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$FOCUSED_ION: PRECURSOR_M/Z 857.52
MS$FOCUSED_ION: PRECURSOR_TYPE [M-H]-
MS$DATA_PROCESSING: WHOLE Xcalibur ver-2.0

PK$SPLASH: splash10-0udi-0046091000-02dc678ad7ee67a4d5ab
PK$ANNOTATION: m/z num type mass error(ppm) formula
  255.05 1 [fa(16:0)-H]- 255.2324052393 -714 C16H31O2-
  259.05 1 [fa(20:4)-H-CO2]- 259.2425759951 -742 C19H31-
  303.13 1 [fa(20:4)-H]- 303.2324052393 -337 C20H31O2-
  553.03 1 [lyso_PI(16:0,-)-H2O]- 553.2777738297 -447 C25H46O11P-
  571.14 1 [lyso_PI(16:0,-)]- 571.288338516 -259 C25H48O12P-
  601.05 1 [lyso_PI(-,20:4)-H2O]- 601.2777738297 -378 C29H46O11P-
  619.03 1 [lyso_PI(-,20:4)]- 619.288338516 -416 C29H48O12P-
PK$NUM_PEAK: 37
PK$PEAK: m/z int. rel.int.
  240.95 425.7 52
  241.80 78.3 10
  255.05 3156.5 384
  256.14 423.1 51
  259.05 243.8 30
  260.01 73.6 9
  285.07 26.0 3
  296.92 1408.1 171
  298.08 201.0 24
  303.13 2415.2 293
  304.08 252.8 31
  314.94 272.7 33
  316.19 40.8 5
  332.38 25.7 3
  332.98 16.2 2
  390.94 4971.2 604
  392.07 514.1 62
  409.06 286.2 35
  410.08 32.0 4
  438.97 783.7 95
  440.05 178.3 22
  461.31 28.4 3
  497.50 23.7 3
  545.26 15.1 2
  553.03 8221.6 999
  553.99 1879.0 228
  554.60 21.3 3
  571.14 2045.2 249
  572.10 417.4 51
  601.05 1577.7 192
  602.00 391.6 48
  619.03 229.2 28
  695.26 73.6 9
  767.33 47.8 6
  770.43 35.8 4
  774.77 37.0 4
  775.37 57.5 7
//

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