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MassBank Record: MSBNK-Chubu_Univ-UT002835

Phosphatidylethanolamine 16:1-18:1; LC-ESI-ITFT; MS2; [M-H]-; RT: 18.83; Exp: 3

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

ACCESSION: MSBNK-Chubu_Univ-UT002835
RECORD_TITLE: Phosphatidylethanolamine 16:1-18:1; LC-ESI-ITFT; MS2; [M-H]-; RT: 18.83; Exp: 3
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$NAME: Phosphatidylethanolamine 16:1-18:1
CH$COMPOUND_CLASS: Natural Product; Glycerophospholipids; Glycerophosphoethanolamines; Diacylglycerophosphoethanolamines
CH$FORMULA: C39H74NO8P
CH$EXACT_MASS: 715.51520
CH$SMILES: C(CCCCCCCCC=CCCC(=O)OC(COP(OCCN)(O)=O)COC(=O)CCC=CCCCCCCCCCCC)CCCC
CH$IUPAC: InChI=1S/C39H74NO8P/c1-3-5-7-9-11-13-15-17-18-20-22-24-26-28-30-32-39(42)48-37(36-47-49(43,44)46-34-33-40)35-45-38(41)31-29-27-25-23-21-19-16-14-12-10-8-6-4-2/h25-28,37H,3-24,29-36,40H2,1-2H3,(H,43,44)/b27-25-,28-26-
CH$LINK: INCHIKEY HGDJXBPLHZFXGO-LBXGSASVSA-N
SP$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$CHROMATOGRAPHY: RETENTION_TIME 18.64 min (in paper: 18.8 min)
AC$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$FOCUSED_ION: PRECURSOR_M/Z 714.51
MS$FOCUSED_ION: PRECURSOR_TYPE [M-H]-
MS$DATA_PROCESSING: WHOLE Xcalibur ver-2.0

PK$SPLASH: splash10-0ue9-0090100000-a3e99b7d6a00688c662b
PK$ANNOTATION: m/z num type mass error(ppm) formula
  253.02 1 [fa(16:1)-H]- 253.2167551751 -776 C16H29O2-
  281.22 1 [fa(18:1)-H]- 281.2480553035 -99 C18H33O2-
  450.05 1 [lyso_PE(16:1,-)]- 450.262064186 -470 C21H41NO7P-
  478.15 1 [lyso_PE(-,18:1)]- 478.2933643144 -299 C23H45NO7P-
PK$NUM_PEAK: 14
PK$PEAK: m/z int. rel.int.
  253.02 503.6 999
  254.03 89.8 178
  281.22 424.5 842
  282.26 19.9 39
  403.13 5.7 11
  450.05 103.6 206
  478.15 57.2 113
  550.97 10.2 20
  551.90 4.6 9
  552.66 28.8 57
  610.67 5.1 10
  623.77 12.5 25
  624.82 29.7 59
  626.03 23.2 46
//

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