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MassBank Record: MSBNK-Chubu_Univ-UT002687

Phosphatidylglyceride 18:1-22:6; LC-ESI-ITFT; MS2; [M-H]-; RT: 9.11; Exp: 3

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

ACCESSION: MSBNK-Chubu_Univ-UT002687
RECORD_TITLE: Phosphatidylglyceride 18:1-22:6; LC-ESI-ITFT; MS2; [M-H]-; RT: 9.11; 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$NAME: Phosphatidylglyceride 18:1-22:6
CH$COMPOUND_CLASS: Natural Product; Glycerophospholipids; Glycerophosphoglycerols; Diacylglycerophosphoglycerols
CH$FORMULA: C46H77O10P
CH$EXACT_MASS: 820.52544
CH$SMILES: C(CC=CCC=CCC=CCC=CCC=CCC=CCC)C(OC(COP(OCC(CO)O)(O)=O)COC(=O)CCC=CCCCCCCCCCCCCC)=O
CH$IUPAC: InChI=1S/C46H77O10P/c1-3-5-7-9-11-13-15-17-19-20-21-22-24-26-28-30-32-34-36-38-46(50)56-44(42-55-57(51,52)54-40-43(48)39-47)41-53-45(49)37-35-33-31-29-27-25-23-18-16-14-12-10-8-6-4-2/h5,7,11,13,17,19,21-22,26,28,31-34,43-44,47-48H,3-4,6,8-10,12,14-16,18,20,23-25,27,29-30,35-42H2,1-2H3,(H,51,52)/b7-5-,13-11-,19-17-,22-21-,28-26-,33-31-,34-32-
CH$LINK: INCHIKEY VGGGUMPTGJTNFQ-QRPORDCISA-N
SP$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: 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$CHROMATOGRAPHY: RETENTION_TIME 9.30 min (in paper: 9.1 min)
AC$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$FOCUSED_ION: PRECURSOR_M/Z 819.52
MS$FOCUSED_ION: PRECURSOR_TYPE [M-H]-
MS$DATA_PROCESSING: WHOLE Xcalibur ver-2.0

PK$SPLASH: splash10-003r-0094010000-234287c97af85c9a2e32
PK$ANNOTATION: m/z num type mass error(ppm) formula
  281.18 1 [fa(18:1)-H]- 281.2480553035 -241 C18H33O2-
  283.13 1 [fa(22:6)-H-CO2]- 283.2425759951 -396 C21H31-
  327.06 1 [fa(22:6)-H]- 327.2324052393 -526 C22H31O2-
  509.32 1 [lyso_PG(18:1,-)]- 509.2879445855 63 C24H46O9P-
  537.03 1 [lyso_PG(-,22:6)-H2O]- 537.261729835 -430 C28H42O8P-
  555.04 1 [lyso_PG(-,22:6)]- 555.2722945213 -417 C28H44O9P-
PK$NUM_PEAK: 18
PK$PEAK: m/z int. rel.int.
  249.24 19.1 33
  281.18 585.6 999
  282.22 14.9 25
  283.13 98.9 169
  284.54 13.9 24
  305.03 8.3 14
  309.15 11.8 20
  327.06 294.9 503
  328.22 60.2 103
  462.89 33.1 56
  464.16 16.6 28
  509.32 39.8 68
  510.18 22.9 39
  537.03 15.0 26
  538.65 6.6 11
  555.04 24.6 42
  759.53 21.6 37
  788.16 25.7 44
//

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