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MassBank Record: MSBNK-Chubu_Univ-UT002394

Phosphatidylcholine 16:0-15:0; LC-ESI-ITFT; MS3; [M+CH3COO]-/[M-CH3]-; RT: 23.16; Exp: 2

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

ACCESSION: MSBNK-Chubu_Univ-UT002394
RECORD_TITLE: Phosphatidylcholine 16:0-15:0; LC-ESI-ITFT; MS3; [M+CH3COO]-/[M-CH3]-; RT: 23.16; Exp: 2
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$NAME: Phosphatidylcholine 16:0-15:0
CH$COMPOUND_CLASS: Natural Product; Glycerophospholipids; Glycerophosphocholines; Diacylglycerophosphocholines
CH$FORMULA: C39H78NO8P
CH$EXACT_MASS: 719.54650
CH$SMILES: C(CCC(=O)OC(COC(=O)CCCCCCCCCCCCCCC)COP([O-1])(=O)OCC[N+1](C)(C)C)CCCCCCCCCCC
CH$IUPAC: InChI=1S/C39H78NO8P/c1-6-8-10-12-14-16-18-20-22-23-25-27-29-31-38(41)45-35-37(36-47-49(43,44)46-34-33-40(3,4)5)48-39(42)32-30-28-26-24-21-19-17-15-13-11-9-7-2/h37H,6-36H2,1-5H3
CH$LINK: INCHIKEY NPGWXTIWUUFYAB-UHFFFAOYSA-N
CH$LINK: PUBCHEM CID:10122972
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$MASS_SPECTROMETRY: MS_TYPE MS3
AC$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$CHROMATOGRAPHY: RETENTION_TIME 23.46 min (in paper: 23.1 min)
AC$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$FOCUSED_ION: PRECURSOR_M/Z 778.56/704.14
MS$FOCUSED_ION: PRECURSOR_TYPE [M+CH3COO]-/[M-CH3]-
MS$DATA_PROCESSING: WHOLE Xcalibur ver-2.0

PK$SPLASH: splash10-052f-0090100000-c724e6fea1101fdcb5c5
PK$ANNOTATION: m/z num type mass error(ppm) formula
  241.01 1 [fa(15:0)-H]- 241.2167551751 -856 C15H29O2-
  255.17 1 [fa(16:0)-H]- 255.2324052393 -244 C16H31O2-
  448.22 1 [lyso_PC(-,15:0)-H2O]- 448.2827996281 -139 C22H43NO6P-
  462.44 1 [lyso_PC(16:0,-)-H2O]- 462.2984496923 306 C23H45NO6P-
  466.11 1 [lyso_PC(-,15:0)]- 466.2933643144 -392 C22H45NO7P-
  480.15 1 [lyso_PC(16:0,-)]- 480.3090143786 -330 C23H47NO7P-
PK$NUM_PEAK: 10
PK$PEAK: m/z int. rel.int.
  224.01 12.6 11
  227.17 42.6 36
  241.01 1170.7 999
  241.72 21.2 18
  255.17 916.5 782
  268.88 7.8 7
  448.22 22.1 19
  462.44 19.3 16
  466.11 113.9 97
  480.15 189.6 162
//

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