Maintenance 2022-01-29. All services on msbi.ipb-halle.de may experience downtime
MassBank MassBank Search Contents Download

MassBank Record: UT001333

Phosphatidylcholine alkyl 16:0-16:0; LC-ESI-ITFT; MS2; [M+CH3COO]-; RT: 33.11; Exp: 1

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

ACCESSION: UT001333
RECORD_TITLE: Phosphatidylcholine alkyl 16:0-16:0; LC-ESI-ITFT; MS2; [M+CH3COO]-; RT: 33.11; 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$NAME: Phosphatidylcholine alkyl 16:0-16:0
CH$COMPOUND_CLASS: Natural Product; Glycerophospholipids; Glycerophosphocholines; 1-alkyl,2-acylglycerophosphocholines
CH$FORMULA: C40H82NO7P
CH$EXACT_MASS: 719.58289
CH$SMILES: C(CCCCCCCCCCCCCC)COCC(OC(CCCCCCCCCCCCCCC)=O)COP([O-1])(=O)OCC[N+1](C)(C)C
CH$IUPAC: InChI=1S/C40H82NO7P/c1-6-8-10-12-14-16-18-20-22-24-26-28-30-32-35-45-37-39(38-47-49(43,44)46-36-34-41(3,4)5)48-40(42)33-31-29-27-25-23-21-19-17-15-13-11-9-7-2/h39H,6-38H2,1-5H3
CH$LINK: CAS 64710-48-1
CH$LINK: INCHIKEY WOTHHEHCEYHCFE-UHFFFAOYSA-N
CH$LINK: PUBCHEM CID:10169139
SP$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$CHROMATOGRAPHY: RETENTION_TIME 33.23 min (in paper: 32.9 min)
AC$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$FOCUSED_ION: PRECURSOR_M/Z 778.60
MS$FOCUSED_ION: PRECURSOR_TYPE [M+CH3COO]-
MS$DATA_PROCESSING: WHOLE Xcalibur ver-2.0

PK$SPLASH: splash10-0udi-0001000900-d33079ab556e71fc6046
PK$ANNOTATION: m/z num type mass error(ppm) formula
  255.05 1 [fa(16:0)-H]- 255.2324052393 -714 C16H31O2-
  436.13 1 [lyso_PC(-,16:0)-CO2]- 436.3191851344 -433 C22H47NO5P-
  448.09 1 [lyso_PC(alkyl-16:0,-)-H2O]- 448.3191851344 -510 C23H47NO5P-
  466.18 1 [lyso_PC(alkyl-16:0,-)]- 466.3297498207 -320 C23H49NO6P-
PK$NUM_PEAK: 30
PK$PEAK: m/z int. rel.int.
  232.25 14.3 3
  251.21 4.7 1
  255.05 33.1 6
  284.35 21.0 4
  285.26 24.0 4
  286.22 59.2 10
  288.20 23.2 4
  329.18 393.4 69
  330.13 171.4 30
  331.08 138.8 24
  333.15 63.6 11
  335.08 7.0 1
  357.18 11.5 2
  359.26 441.8 77
  360.25 32.1 6
  436.13 101.8 18
  437.13 23.8 4
  446.51 51.5 9
  447.27 26.3 5
  448.09 7.5 1
  464.62 28.0 5
  465.24 100.8 18
  466.18 105.1 18
  466.84 10.3 2
  467.55 6.9 1
  596.56 10.4 2
  704.18 5708.2 999
  704.95 46.3 8
  718.98 34.4 6
  736.23 11.5 2
//

system version 2.1.10-SNAPSHOT
Copyright © 2006 MassBank Project; 2011 NORMAN Association; 2021 MassBank Consortium