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MassBank Record: MSBNK-Chubu_Univ-UT002877

Phosphatidylethanolamine alkenyl 16:0-20:5; LC-ESI-ITFT; MS2; [M-H]-; RT: 18.06; Exp: 3

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

ACCESSION: MSBNK-Chubu_Univ-UT002877
RECORD_TITLE: Phosphatidylethanolamine alkenyl 16:0-20:5; LC-ESI-ITFT; MS2; [M-H]-; RT: 18.06; 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$NAME: Phosphatidylethanolamine alkenyl 16:0-20:5
CH$COMPOUND_CLASS: Natural Product; Glycerophospholipids; Glycerophosphoethanolamines; 1Z-alkenyl,2-acylglycerophosphoethanolamines
CH$FORMULA: C41H72NO7P
CH$EXACT_MASS: 721.50464
CH$SMILES: C(=COCC(OC(CCC=CCC=CCC=CCC=CCC=CCCC)=O)COP(O)(=O)OCCN)CCCCCCCCCCCCCC
CH$IUPAC: InChI=1S/C41H72NO7P/c1-3-5-7-9-11-13-15-17-19-20-21-22-24-26-28-30-32-34-41(43)49-40(39-48-50(44,45)47-37-35-42)38-46-36-33-31-29-27-25-23-18-16-14-12-10-8-6-4-2/h7,9,13,15,19-20,22,24,28,30,33,36,40H,3-6,8,10-12,14,16-18,21,23,25-27,29,31-32,34-35,37-39,42H2,1-2H3,(H,44,45)/b9-7-,15-13-,20-19-,24-22-,30-28-,36-33+
CH$LINK: INCHIKEY RPMVRPOBBVLOLS-HAQSCEBBSA-N
SP$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$CHROMATOGRAPHY: RETENTION_TIME 18.14 min (in paper: 18.1 min)
AC$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$FOCUSED_ION: PRECURSOR_M/Z 720.50
MS$FOCUSED_ION: PRECURSOR_TYPE [M-H]-
MS$DATA_PROCESSING: WHOLE Xcalibur ver-2.0

PK$SPLASH: splash10-0udi-0009500000-6e610146f87454782a01
PK$ANNOTATION: m/z num type mass error(ppm) formula
  256.96 1 [fa(20:5)-H-CO2]- 257.2269259309 -1037 C19H29-
  301.07 1 [fa(20:5)-H]- 301.2167551751 -486 C20H29O2-
  418.03 1 [lyso_PE(alkenyl-16:0,-)-H2O]- 418.2722349418 -578 C21H41NO5P-
  436.20 1 [lyso_PE(alkenyl-16:0,-)]- 436.2827996281 -189 C21H43NO6P-
PK$NUM_PEAK: 19
PK$PEAK: m/z int. rel.int.
  256.96 21.5 61
  281.25 4.0 11
  283.26 11.0 31
  301.07 350.7 999
  302.10 35.8 102
  302.99 33.6 96
  304.13 6.8 19
  417.42 14.8 42
  418.03 28.3 81
  427.98 19.5 56
  434.23 18.2 52
  436.20 148.6 423
  436.95 10.8 31
  464.56 7.4 21
  479.90 4.6 13
  575.92 6.8 19
  631.38 15.7 45
  638.05 27.2 77
  700.53 8.0 23
//

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