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MassBank Record: MSBNK-Chubu_Univ-UT002205

Phosphatidylglyceride 16:0-20:4; LC-ESI-ITFT; MS2; [M-H]-; RT: 14.40; Exp: 2

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

ACCESSION: MSBNK-Chubu_Univ-UT002205
RECORD_TITLE: Phosphatidylglyceride 16:0-20:4; LC-ESI-ITFT; MS2; [M-H]-; RT: 14.40; Exp: 2
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$NAME: Phosphatidylglyceride 16:0-20:4
CH$COMPOUND_CLASS: Natural Product; Glycerophospholipids; Glycerophosphoglycerols; Diacylglycerophosphoglycerols
CH$FORMULA: C42H75O10P
CH$EXACT_MASS: 770.50979
CH$SMILES: C(CCCC(=O)OCC(COP(OCC(O)CO)(O)=O)OC(=O)CCC=CCC=CCC=CCC=CCCCCCC)CCCCCCCCCCC
CH$IUPAC: InChI=1S/C42H75O10P/c1-3-5-7-9-11-13-15-17-18-19-20-22-24-26-28-30-32-34-42(46)52-40(38-51-53(47,48)50-36-39(44)35-43)37-49-41(45)33-31-29-27-25-23-21-16-14-12-10-8-6-4-2/h13,15,18-19,22,24,28,30,39-40,43-44H,3-12,14,16-17,20-21,23,25-27,29,31-38H2,1-2H3,(H,47,48)/b15-13-,19-18-,24-22-,30-28-
CH$LINK: INCHIKEY UAEIOGMLUFANFU-WRDNLCFKSA-N
SP$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$CHROMATOGRAPHY: RETENTION_TIME 14.35 min (in paper: 14.4 min)
AC$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$FOCUSED_ION: PRECURSOR_M/Z 769.50
MS$FOCUSED_ION: PRECURSOR_TYPE [M-H]-
MS$DATA_PROCESSING: WHOLE Xcalibur ver-2.0

PK$SPLASH: splash10-0udi-0039200000-132784ac6b4092585fe8
PK$ANNOTATION: m/z num type mass error(ppm) formula
  255.13 1 [fa(16:0)-H]- 255.2324052393 -400 C16H31O2-
  259.06 1 [fa(20:4)-H-CO2]- 259.2425759951 -703 C19H31-
  303.09 1 [fa(20:4)-H]- 303.2324052393 -469 C20H31O2-
  439.15 1 [lyso_PG(16:0,-)-CO2]- 439.2824652771 -301 C21H44O7P-
  465.07 1 [lyso_PG(16:0,-)-H2O]- 465.261729835 -411 C22H42O8P-
  483.03 1 [lyso_PG(16:0,-)]- 483.2722945213 -500 C22H44O9P-
PK$NUM_PEAK: 28
PK$PEAK: m/z int. rel.int.
  234.84 3.4 4
  249.17 14.4 17
  255.13 207.8 248
  256.03 36.2 43
  259.06 16.5 20
  283.16 123.6 148
  303.09 836.2 999
  304.16 82.6 99
  326.45 13.2 16
  327.25 115.6 138
  368.52 9.9 12
  388.88 20.0 24
  390.97 83.6 100
  391.98 39.0 47
  439.15 46.9 56
  440.23 12.3 15
  441.72 12.7 15
  460.03 81.1 97
  465.07 53.0 63
  466.03 7.0 8
  483.03 130.2 156
  484.11 43.3 52
  505.99 12.5 15
  512.91 20.8 25
  708.46 32.8 39
  709.20 7.0 8
  723.47 15.6 19
  726.66 15.8 19
//

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