ACCESSION: MSBNK-Chubu_Univ-UT000100
RECORD_TITLE: 15-HEPE; LC-ESI-QIT; MS2; CE:10 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$NAME: 15-HEPE
CH$NAME: 15-hydroxy-5Z,8Z,11Z,13E,17Z-eicosapentaenoic acid
CH$NAME: (5Z,8Z,11Z,14Z,17Z)-15-Hydroxy-5,8,11,14,17-icosapentaenoic acid
CH$NAME: (+-)15-HEPE
CH$COMPOUND_CLASS: Natural Product; Lipid; Fatty acid
CH$FORMULA: C₂₀H₃₀O₃
CH$EXACT_MASS: 318.21949
CH$SMILES: CCC=CCC(O)C=CC=CCC=CCC=CCCCC(O)=O
CH$IUPAC: InChI=1S/C20H30O3/c1-2-3-13-16-19(21)17-14-11-9-7-5-4-6-8-10-12-15-18-20(22)23/h3-5,8-11,13-14,17,19,21H,2,6-7,12,15-16,18H2,1H3,(H,22,23)/b5-4-,10-8-,11-9-,13-3-,17-14+/t19-/m0/s1
CH$LINK: CAS 88852-33-9
CH$LINK: CAYMAN 32700
CH$LINK: LIPIDBANK DFA8126
CH$LINK: NIKKAJI J1.881.939B
CH$LINK: INCHIKEY WLKCSMCLEKGITB-DBVSHIMFSA-N

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$MASS_SPECTROMETRY: COLLISION_ENERGY 10 V
AC$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$SPLASH: splash10-014i-0029000000-9c262259fc19dbd163b5
PK$NUM_PEAK: 27
PK$PEAK: m/z int. rel.int.
  147.200 15625.0 1
  162.880 9375.0 1
  163.188 168750.0 10
  175.216 393750.0 23
  201.200 12500.0 1
  203.224 143750.0 8
  203.520 9375.0 1
  205.129 112500.0 7
  205.440 18750.0 1
  219.165 762500.0 45
  247.182 200000.0 12
  248.184 53125.0 3
  248.720 9375.0 1
  255.232 2234375.0 132
  256.080 21875.0 1
  256.720 18750.0 1
  273.333 93750.0 6
  273.520 15625.0 1
  274.160 12500.0 1
  281.340 15625.0 1
  299.203 1100000.0 65
  299.680 18750.0 1
  300.080 18750.0 1
  300.240 18750.0 1
  315.280 21875.0 1
  317.136 16965625.0 999
  317.840 12500.0 1
//