ACCESSION: MSBNK-Chubu_Univ-UT000069
RECORD_TITLE: 13-HPODE; LC-ESI-QIT; MS2; CE:35 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$NAME: 13-HPODE
CH$NAME: 13S-hydroperoxy-9Z,11E-octadecadienoic acid
CH$NAME: 13-Hydroperoxyoctadeca-9,11-dienoic acid
CH$NAME: 13(S)-HpODE
CH$NAME: (9Z,11E)-(13S)-13-Hydroperoxyoctadeca-9,11-dienoate
CH$NAME: (9Z,11E)-(13S)-13-Hydroperoxyoctadeca-9,11-dienoic acid
CH$NAME: 13(S)-HPODE
CH$NAME: 13S-Hydroperoxy-9Z,11E-octadecadienoic acid
CH$COMPOUND_CLASS: Natural Product; Lipid; Fatty acid
CH$FORMULA: C₁₈H₃₂O₄
CH$EXACT_MASS: 312.23006
CH$SMILES: CCCCCC(OO)C=CC=CCCCCCCCC(O)=O
CH$IUPAC: InChI=1S/C18H32O4/c1-2-3-11-14-17(22-21)15-12-9-7-5-4-6-8-10-13-16-18(19)20/h7,9,12,15,17,21H,2-6,8,10-11,13-14,16H2,1H3,(H,19,20)/b9-7?,15-12+
CH$LINK: CAS 33964-75-9
CH$LINK: CAYMAN 48610
CH$LINK: CHEBI 15655
CH$LINK: KEGG C04717
CH$LINK: LIPIDBANK DFA8002
CH$LINK: NIKKAJI J360.976F
CH$LINK: PUBCHEM CID:7289
CH$LINK: INCHIKEY JDSRHVWSAMTSSN-WWYDAZRDSA-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$MASS_SPECTROMETRY: COLLISION_ENERGY 35 V
AC$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$SPLASH: splash10-03ka-0291000000-17440de6012836f1b0ae
PK$NUM_PEAK: 16
PK$PEAK: m/z int. rel.int.
  141.280 6250.0 171
  149.200 9375.0 257
  183.040 9375.0 257
  195.120 15625.0 428
  197.120 9375.0 257
  205.011 32291.7 885
  211.120 30208.3 828
  211.280 15625.0 428
  222.880 15625.0 428
  223.104 36458.3 999
  223.280 6250.0 171
  249.040 15625.0 428
  265.240 9375.0 257
  291.200 6250.0 171
  293.243 13541.7 371
  311.120 27083.3 742
//