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MassBank Record: MSBNK-Chubu_Univ-UT000070

13-HPODE; LC-ESI-QIT; MS2; CE:40 V; [M-H]-

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

ACCESSION: MSBNK-Chubu_Univ-UT000070
RECORD_TITLE: 13-HPODE; LC-ESI-QIT; MS2; CE:40 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$MASS_SPECTROMETRY: COLLISION_ENERGY 40 V
AC$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$SPLASH: splash10-00di-0590000000-1646e7b0c7ddcd7420a1
PK$NUM_PEAK: 6
PK$PEAK: m/z int. rel.int.
  171.040 9375.0 375
  182.960 9375.0 375
  194.960 6250.0 250
  205.040 6250.0 250
  223.067 25000.0 999
  293.120 9375.0 375
//

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