ACCESSION: MSBNK-Chubu_Univ-UT002151
RECORD_TITLE: Phosphatidylethanolamine alkenyl 16:0-22:6; LC-ESI-ITFT; MS2; [M-H]-; RT: 20.47; 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$NAME: Phosphatidylethanolamine alkenyl 16:0-22:6
CH$COMPOUND_CLASS: Natural Product; Glycerophospholipids; Glycerophosphoethanolamines; 1Z-alkenyl,2-acylglycerophosphoethanolamines
CH$FORMULA: C43H74NO7P
CH$EXACT_MASS: 747.52029
CH$SMILES: NCCOP(O)(=O)OCC(COC=CCCCCCCCCCCCCCC)OC(=O)CCC=CCC=CCC=CCC=CCC=CCC=CCC
CH$IUPAC: InChI=1S/C43H74NO7P/c1-3-5-7-9-11-13-15-17-19-20-21-22-23-24-26-28-30-32-34-36-43(45)51-42(41-50-52(46,47)49-39-37-44)40-48-38-35-33-31-29-27-25-18-16-14-12-10-8-6-4-2/h5,7,11,13,17,19,21-22,24,26,30,32,35,38,42H,3-4,6,8-10,12,14-16,18,20,23,25,27-29,31,33-34,36-37,39-41,44H2,1-2H3,(H,46,47)/b7-5-,13-11-,19-17-,22-21-,26-24-,32-30-,38-35+
CH$LINK: CAS
139406-72-7
CH$LINK: INCHIKEY
WVGALBKSWOUIEZ-ULUZTLKMSA-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$CHROMATOGRAPHY: RETENTION_TIME 20.57 min (in paper: 20.5 min)
AC$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 746.51
MS$FOCUSED_ION: PRECURSOR_TYPE [M-H]-
MS$DATA_PROCESSING: WHOLE Xcalibur ver-2.0
PK$SPLASH: splash10-005i-0069800000-961fe4a7097d10537fc9
PK$ANNOTATION: m/z num type mass error(ppm) formula
239.18 1 [fa(alkenyl-16:0)-H]- 239.2374906172 -239 C16H31O-
283.15 1 [fa(22:6)-H-CO2]- 283.2425759951 -326 C21H31-
327.08 1 [fa(22:6)-H]- 327.2324052393 -465 C22H31O2-
418.18 1 [lyso_PE(alkenyl-16:0,-)-H2O]- 418.2722349418 -220 C21H41NO5P-
436.10 1 [lyso_PE(alkenyl-16:0,-)]- 436.2827996281 -418 C21H43NO6P-
PK$NUM_PEAK: 25
PK$PEAK: m/z int. rel.int.
212.50 97.8 2
228.96 718.3 16
230.15 181.5 4
239.18 161.2 4
241.19 63.6 1
249.05 196.0 4
255.11 1836.2 40
281.16 4178.4 91
283.15 25469.8 554
284.21 1334.8 29
307.05 52.8 1
309.12 460.7 10
325.26 76.5 2
327.08 45961.5 999
327.96 3354.7 73
375.07 387.4 8
391.00 876.1 19
418.18 4809.7 105
419.28 671.5 15
436.10 36007.8 783
437.04 3598.4 78
464.99 492.5 11
483.05 659.8 14
491.11 133.0 3
505.96 129.4 3
//
