MassBank Record: UT000292



 LTB4_20-Hydroxy; LC-ESI-QIT; MS2; CE:25 V; [M-H]- 
Mass Spectrum
Chemical Structure
Generated by the Chemistry Development Kit (http://github.com/cdk) \n

ACCESSION: UT000292
RECORD_TITLE: LTB4_20-Hydroxy; LC-ESI-QIT; MS2; CE:25 V; [M-H]-
DATE: 2016.01.19 (Created 2007.10.19, modified 2011.08.03)
AUTHORS: Nakanishi H, Taguchi R, Graduate School of Medicine, The University of Tokyo.
LICENSE: CC BY-NC-SA

CH$NAME: LTB4_20-Hydroxy CH$NAME: 5S,12R,20-trihydroxy-6Z,8E,10E,14Z-eicosatetraenoic acid CH$NAME: (5R,12S,6Z,8E,10E,14Z)-5,12,20-Trihydroxy-6,8,10,14-icosatetraenoic acid CH$NAME: 20-hydroxy LTB4 CH$COMPOUND_CLASS: Natural Product; Lipid; Eicosanoid CH$FORMULA: C20H32O5 CH$EXACT_MASS: 352.22497 CH$SMILES: OCCCCCC=CCC(O)C=CC=CC=CC(O)CCCC(O)=O CH$IUPAC: InChI=1S/C20H32O5/c21-17-10-6-2-1-3-7-12-18(22)13-8-4-5-9-14-19(23)15-11-16-20(24)25/h3-5,7-9,13-14,18-19,21-23H,1-2,6,10-12,15-17H2,(H,24,25)/b5-4+,7-3-,13-8+,14-9-/t18-,19-/m1/s1 CH$LINK: CAS 79516-82-8 CH$LINK: CAYMAN 20190 CH$LINK: LIPIDBANK XPR3120 CH$LINK: NIKKAJI J381.079H
AC$INSTRUMENT: 4000Q TRAP, Applied Biosystems AC$INSTRUMENT_TYPE: LC-ESI-QIT AC$MASS_SPECTROMETRY: MS_TYPE MS2 AC$MASS_SPECTROMETRY: ION_MODE NEGATIVE AC$MASS_SPECTROMETRY: COLLISION_ENERGY 25 V AC$MASS_SPECTROMETRY: IONIZATION ESI
MS$FOCUSED_ION: PRECURSOR_TYPE [M-H]- MS$DATA_PROCESSING: IGNORE rel.val. < 0.5 MS$DATA_PROCESSING: WHOLE Analyst 1.4.2
PK$SPLASH: splash10-0udi-0109000000-e01ef44cb36e9df489f9 PK$NUM_PEAK: 27 PK$PEAK: m/z int. rel.int. 106.960 34375.0 6 123.013 21875.0 4 150.800 12500.0 2 151.145 100000.0 18 161.160 81250.0 14 177.068 90625.0 16 181.149 15625.0 3 189.120 12500.0 2 195.073 1253125.0 220 205.120 21875.0 4 217.280 6250.0 1 219.120 21875.0 4 235.120 12500.0 2 255.120 9375.0 2 261.200 87500.0 15 271.120 15625.0 3 273.120 9375.0 2 283.120 9375.0 2 289.120 131250.0 23 297.100 12500.0 2 303.120 9375.0 2 315.147 112500.0 20 315.360 15625.0 3 333.124 1475000.0 259 333.600 15625.0 3 351.125 5681250.0 999 352.080 6250.0 1 //