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MassBank Record: MSBNK-Chubu_Univ-UT001210

Phosphatidylglyceride 18:1-20:4; LC-ESI-ITFT; MS2; [M-H]-; RT: 10.09; Exp: 1

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

ACCESSION: MSBNK-Chubu_Univ-UT001210
RECORD_TITLE: Phosphatidylglyceride 18:1-20:4; LC-ESI-ITFT; MS2; [M-H]-; RT: 10.09; Exp: 1
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$NAME: Phosphatidylglyceride 18:1-20:4
CH$COMPOUND_CLASS: Natural Product; Glycerophospholipids; Glycerophosphoglycerols; Diacylglycerophosphoglycerols
CH$FORMULA: C44H77O10P
CH$EXACT_MASS: 796.52544
CH$SMILES: C(CCCCCC)=CCC=CCC=CCC=CCCC(OC(COC(=O)CCC=CCCCCCCCCCCCCC)COP(O)(=O)OCC(O)CO)=O
CH$IUPAC: InChI=1S/C44H77O10P/c1-3-5-7-9-11-13-15-17-19-20-22-24-26-28-30-32-34-36-44(48)54-42(40-53-55(49,50)52-38-41(46)37-45)39-51-43(47)35-33-31-29-27-25-23-21-18-16-14-12-10-8-6-4-2/h13,15,19-20,24,26,29-32,41-42,45-46H,3-12,14,16-18,21-23,25,27-28,33-40H2,1-2H3,(H,49,50)/b15-13-,20-19-,26-24-,31-29-,32-30-
CH$LINK: INCHIKEY ITIOHRDVKOPUBF-MOYSMJPMSA-N
SP$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$CHROMATOGRAPHY: RETENTION_TIME 10.02 min (in paper: 10.1 min)
AC$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$FOCUSED_ION: PRECURSOR_M/Z 795.52
MS$FOCUSED_ION: PRECURSOR_TYPE [M-H]-
MS$DATA_PROCESSING: WHOLE Xcalibur ver-2.0

PK$SPLASH: splash10-0f89-0089111700-2535e12fbed425b696bf
PK$ANNOTATION: m/z num type mass error(ppm) formula
  259.47 1 [fa(20:4)-H-CO2]- 259.2425759951 877 C19H31-
  281.04 1 [fa(18:1)-H]- 281.2480553035 -739 C18H33O2-
  303.06 1 [fa(20:4)-H]- 303.2324052393 -568 C20H31O2-
  491.21 1 [lyso_PG(18:1,-)-H2O]- 491.2773798992 -136 C24H44O8P-
  509.16 1 [lyso_PG(18:1,-)]- 509.2879445855 -250 C24H46O9P-
  530.98 1 [lyso_PG(-,20:4)]- 531.2722945213 -549 C26H44O9P-
PK$NUM_PEAK: 19
PK$PEAK: m/z int. rel.int.
  259.47 18.9 83
  260.13 6.5 28
  281.04 192.5 842
  282.17 10.0 44
  303.06 228.3 999
  304.29 5.9 26
  447.02 6.5 28
  452.07 11.6 51
  488.91 6.6 29
  491.21 7.6 33
  509.16 16.2 71
  530.98 18.9 83
  568.24 12.7 56
  630.31 7.0 31
  668.74 20.3 89
  676.36 14.3 63
  730.66 142.1 622
  731.81 45.6 200
  777.14 4.8 21
//

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