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MassBank Record: MSBNK-Chubu_Univ-UT001011

Phosphatidylcholine 16:0-16:0; LC-ESI-ITFT; MS2; [M+CH3COO]-; RT: 26.91; Exp: 1

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

ACCESSION: MSBNK-Chubu_Univ-UT001011
RECORD_TITLE: Phosphatidylcholine 16:0-16:0; LC-ESI-ITFT; MS2; [M+CH3COO]-; RT: 26.91; 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$NAME: Phosphatidylcholine 16:0-16:0
CH$COMPOUND_CLASS: Natural Product; Glycerophospholipids; Glycerophosphocholines; Diacylglycerophosphocholines
CH$FORMULA: C40H80NO8P
CH$EXACT_MASS: 733.56216
CH$SMILES: C(CCCCCCCCC)CCCCCC(=O)OCC(COP(OCC[N+1](C)(C)C)([O-1])=O)OC(CCCCCCCCCCCCCCC)=O
CH$IUPAC: InChI=1S/C40H80NO8P/c1-6-8-10-12-14-16-18-20-22-24-26-28-30-32-39(42)46-36-38(37-48-50(44,45)47-35-34-41(3,4)5)49-40(43)33-31-29-27-25-23-21-19-17-15-13-11-9-7-2/h38H,6-37H2,1-5H3
CH$LINK: CAS 2644-64-6
CH$LINK: COMPTOX DTXSID50910226
CH$LINK: INCHIKEY KILNVBDSWZSGLL-UHFFFAOYSA-N
CH$LINK: LIPIDBANK PGP2015
CH$LINK: PUBCHEM CID:6138
SP$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$CHROMATOGRAPHY: RETENTION_TIME 26.98 min (in paper: 26.9 min)
AC$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$FOCUSED_ION: PRECURSOR_M/Z 792.57
MS$FOCUSED_ION: PRECURSOR_TYPE [M+CH3COO]-
MS$DATA_PROCESSING: WHOLE Xcalibur ver-2.0

PK$SPLASH: splash10-014i-0000000900-6acb075cc890d1ad974d
PK$ANNOTATION: m/z num type mass error(ppm) formula
  255.15 1 [fa(16:0)-H]- 255.2324052393 -322 C16H31O2-
  480.22 2 [lyso_PC(-,16:0)]- 480.3090143786 -184 C23H47NO7P-
  480.22 2 [lyso_PC(16:0,-)]- 480.3090143786 -184 C23H47NO7P-
PK$NUM_PEAK: 19
PK$PEAK: m/z int. rel.int.
  251.42 18.1 1
  255.15 463.2 8
  283.08 462.9 8
  283.91 22.0 1
  285.04 90.7 1
  286.42 19.5 1
  303.17 210.6 3
  309.04 19.3 1
  329.13 515.0 8
  330.29 66.8 1
  391.24 18.1 1
  480.22 106.2 2
  506.22 32.0 1
  647.28 33.4 1
  718.16 61620.4 999
  718.86 161.0 3
  733.19 148.0 2
  742.20 12.2 1
  775.34 20.7 1
//

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