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MassBank Record: UT000085

13-HpOTrE; LC-ESI-QIT; MS2; CE:25 V; [M-H]-

Mass Spectrum
Chemical Structure
Generated by the Chemistry Development Kit (http://github.com/cdk)

ACCESSION: UT000085
RECORD_TITLE: 13-HpOTrE; 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$NAME: 13-HpOTrE
CH$NAME: 13S-hydroperoxy-9Z,11E,15Z-octadecatrienoic acid
CH$NAME: (9Z,11E,15Z)-13-Hydroperoxy-9,11,15-octadecatrienoic acid
CH$NAME: 13(S)-HpOTrE
CH$COMPOUND_CLASS: Natural Product; Lipid; Fatty acid
CH$FORMULA: C18H30O4
CH$EXACT_MASS: 310.21441
CH$SMILES: CCC=CCC(OO)C=CC=CCCCCCCCC(O)=O
CH$IUPAC: InChI=1S/C18H30O4/c1-2-3-11-14-17(22-21)15-12-9-7-5-4-6-8-10-13-16-18(19)20/h3,7,9,11-12,15,17,21H,2,4-6,8,10,13-14,16H2,1H3,(H,19,20)/b9-7?,11-3-,15-12+
CH$LINK: CAS 67597-26-6
CH$LINK: CAYMAN 45220
CH$LINK: LIPIDBANK DFA8052
CH$LINK: INCHIKEY UYQGVDXDXBAABN-TUAAJWHTSA-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$MASS_SPECTROMETRY: COLLISION_ENERGY 25 V
AC$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$SPLASH: splash10-056u-0191000000-8b918504a2dffe79dff1
PK$NUM_PEAK: 14
PK$PEAK: m/z int. rel.int.
  98.880 6250.0 20
  111.120 15625.0 51
  195.118 114583.3 374
  197.240 3125.0 10
  205.120 18750.0 61
  209.120 72916.7 238
  227.186 306250.0 999
  241.180 9375.0 31
  247.040 27083.3 88
  247.280 28125.0 92
  255.120 18750.0 61
  273.140 9375.0 31
  291.155 192708.3 629
  309.135 118750.0 387
//

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