MassBank Record: UT002905



 Phosphatidylethanolamine alkenyl 18:1-24:4; LC-ESI-ITFT; MS2; [M-H]-; RT: 32.39; Exp: 3 
Mass Spectrum
Chemical Structure
Generated by the Chemistry Development Kit (http://github.com/cdk) \n

ACCESSION: UT002905
RECORD_TITLE: Phosphatidylethanolamine alkenyl 18:1-24:4; LC-ESI-ITFT; MS2; [M-H]-; RT: 32.39; 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. J Chromatogr A (2010), doi:10.1016/j.chroma.2010.04.034 (in press)

CH$NAME: Phosphatidylethanolamine alkenyl 18:1-24:4 CH$COMPOUND_CLASS: Natural Product; "Glycerophospholipids; Glycerophosphoethanolamines; 1Z-alkenyl,2-acylglycerophosphoethanolamines" CH$FORMULA: C47H84NO7P CH$EXACT_MASS: 805.59854 CH$SMILES: C(CCCCCCCCC)CCCC=CCC=COCC(OC(CCC=CCC=CCC=CCC=CCCCCCCCCCC)=O)COP(OCCN)(O)=O CH$IUPAC: InChI=1S/C47H84NO7P/c1-3-5-7-9-11-13-15-17-19-21-22-23-24-25-26-28-30-32-34-36-38-40-47(49)55-46(45-54-56(50,51)53-43-41-48)44-52-42-39-37-35-33-31-29-27-20-18-16-14-12-10-8-6-4-2/h21-22,24-25,28,30,33-36,39,42,46H,3-20,23,26-27,29,31-32,37-38,40-41,43-45,48H2,1-2H3,(H,50,51)/b22-21-,25-24-,30-28-,35-33-,36-34-,42-39+ SP$SCIENTIFIC_NAME: Mus musculus SP$NAME: mouse 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 32.36 min (in paper: 32.4 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$FOCUSED_ION: PRECURSOR_M/Z 804.59 MS$FOCUSED_ION: PRECURSOR_TYPE [M-H]- MS$DATA_PROCESSING: WHOLE Xcalibur ver-2.0
PK$SPLASH: splash10-0a4i-0009200100-9a71e325c78e662e4277 PK$ANNOTATION: m/z num ( type mass error(ppm) formula ) 462.10 1 [lyso PE(alkenyl-18:1,-)]- 462.2984496923 -428 C23H45NO6P- 444.16 1 [lyso PE(alkenyl-18:1,-)-H2O]- 444.287885006 -287 C23H43NO5P- 359.17 1 [fa(24:4)-H]- 359.2950054961 -347 C24H39O2- 315.22 1 [fa(24:4)-H-CO2]- 315.3051762519 -269 C23H39- 265.05 1 [fa(alkenyl-18:1)-H]- 265.2531406814 -765 C18H33O- PK$NUM_PEAK: 14 PK$PEAK: m/z int. rel.int. 265.05 5.7 3 315.22 69.3 41 341.19 19.8 12 359.17 1684.4 999 360.18 391.0 232 362.16 13.4 8 444.16 78.8 47 445.07 27.2 16 462.10 359.3 213 463.15 80.4 48 466.45 8.0 5 717.39 18.5 11 721.61 6.8 4 730.21 271.5 161 //