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MassBank Record: MSBNK-Chubu_Univ-UT002891

Phosphatidylethanolamine alkenyl 18:0-22:1; LC-ESI-ITFT; MS2; [M-H]-; RT: 47.07; Exp: 3

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

ACCESSION: MSBNK-Chubu_Univ-UT002891
RECORD_TITLE: Phosphatidylethanolamine alkenyl 18:0-22:1; LC-ESI-ITFT; MS2; [M-H]-; RT: 47.07; 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$NAME: Phosphatidylethanolamine alkenyl 18:0-22:1
CH$COMPOUND_CLASS: Natural Product; Glycerophospholipids; Glycerophosphoethanolamines; 1Z-alkenyl,2-acylglycerophosphoethanolamines
CH$FORMULA: C45H88NO7P
CH$EXACT_MASS: 785.62984
CH$SMILES: C(CCCCCCCCCCC)CCCCC=COCC(COP(OCCN)(O)=O)OC(CCC=CCCCCCCCCCCCCCCCCC)=O
CH$IUPAC: InChI=1S/C45H88NO7P/c1-3-5-7-9-11-13-15-17-19-21-22-23-24-26-28-30-32-34-36-38-45(47)53-44(43-52-54(48,49)51-41-39-46)42-50-40-37-35-33-31-29-27-25-20-18-16-14-12-10-8-6-4-2/h32,34,37,40,44H,3-31,33,35-36,38-39,41-43,46H2,1-2H3,(H,48,49)/b34-32-,40-37+
CH$LINK: INCHIKEY MIKCEBQQTIVKSQ-LITAQCTLSA-N
SP$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$CHROMATOGRAPHY: RETENTION_TIME 46.93 min (in paper: 47.1 min)
AC$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$FOCUSED_ION: PRECURSOR_M/Z 784.62
MS$FOCUSED_ION: PRECURSOR_TYPE [M-H]-
MS$DATA_PROCESSING: WHOLE Xcalibur ver-2.0

PK$SPLASH: splash10-000i-0009100000-651288d01dba4423504c
PK$ANNOTATION: m/z num type mass error(ppm) formula
  337.16 1 [fa(22:1)-H]- 337.3106555603 -446 C22H41O2-
  446.24 1 [lyso_PE(alkenyl-18:0,-)-H2O]- 446.3035350702 -141 C23H45NO5P-
  464.21 1 [lyso_PE(alkenyl-18:0,-)]- 464.3140997565 -223 C23H47NO6P-
PK$NUM_PEAK: 28
PK$PEAK: m/z int. rel.int.
  255.07 30.3 9
  267.60 20.5 6
  311.29 10.0 3
  337.16 3472.2 999
  338.28 698.1 201
  339.41 30.8 9
  351.06 34.9 10
  365.11 1113.5 320
  366.28 198.4 57
  368.74 10.2 3
  403.05 21.8 6
  404.36 21.9 6
  417.29 25.7 7
  419.01 18.6 5
  436.06 136.9 39
  437.39 27.6 8
  446.24 106.6 31
  447.57 8.3 2
  462.69 27.4 8
  464.21 482.3 139
  465.24 97.9 28
  503.31 5.3 2
  619.57 18.3 5
  629.21 25.9 7
  631.94 13.3 4
  697.96 12.0 3
  702.27 80.8 23
  751.69 7.6 2
//

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