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MassBank Record: MSBNK-MPI_for_Chemical_Ecology-CE000118

Rotenone; LC-ESI-ITFT; MS2; CE 35 eV; [M+H]+

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

ACCESSION: MSBNK-MPI_for_Chemical_Ecology-CE000118
RECORD_TITLE: Rotenone; LC-ESI-ITFT; MS2; CE 35 eV; [M+H]+
DATE: 2016.01.19 (Created 2012.04.11)
AUTHORS: Ales Svatos, Ravi Kumar Maddula, MPI for Chemical Ecology, Jena, Germany
LICENSE: CC BY-NC-SA
COPYRIGHT: Copyright(C) 2011 MPI for Chemical Ecology, Jena, Germany
PUBLICATION: F. Rasche, A. Svatos, R.K. Maddula, C. Boettcher and S. Boecker. Computing fragmentation trees from tandem mass spectrometry data. Anal. Chem., 2011, 83, 1243-1251 doi:10.1021/ac101825k
COMMENT: Acquisition and generation of the data is financially supported by the Max-Planck-Society

CH$NAME: Rotenone
CH$COMPOUND_CLASS: Natural Product; Benzopyran
CH$FORMULA: C23H22O6
CH$EXACT_MASS: 394.14164
CH$SMILES: CC(=C)[C@H]1CC2=C(O1)C=CC3=C2O[C@@H]4COC5=CC(=C(C=C5[C@@H]4C3=O)OC)OC
CH$IUPAC: InChI=1S/C23H22O6/c1-11(2)16-8-14-15(28-16)6-5-12-22(24)21-13-7-18(25-3)19(26-4)9-17(13)27-10-20(21)29-23(12)14/h5-7,9,16,20-21H,1,8,10H2,2-4H3/t16-,20-,21+/m1/s1
CH$LINK: PUBCHEM CID:6758
CH$LINK: INCHIKEY JUVIOZPCNVVQFO-HBGVWJBISA-N
CH$LINK: COMPTOX DTXSID6021248

AC$INSTRUMENT: LTQ Orbitrap XL, Thermo Scientfic; HP-1100 HPLC, Agilent
AC$INSTRUMENT_TYPE: LC-ESI-ITFT
AC$MASS_SPECTROMETRY: MS_TYPE MS2
AC$MASS_SPECTROMETRY: ION_MODE POSITIVE
AC$MASS_SPECTROMETRY: ACTIVATION_PARAMETER q=0.25
AC$MASS_SPECTROMETRY: ACTIVATION_TIME 30 ms
AC$MASS_SPECTROMETRY: AUTOMATIC_GAIN_CONTROL 3.0E5
AC$MASS_SPECTROMETRY: CAPILLARY_TEMPERATURE 275 C
AC$MASS_SPECTROMETRY: CAPILLARY_VOLTAGE 39 V
AC$MASS_SPECTROMETRY: COLLISION_ENERGY 35eV
AC$MASS_SPECTROMETRY: FRAGMENTATION_MODE CID
AC$MASS_SPECTROMETRY: IONIZATION ESI
AC$MASS_SPECTROMETRY: RESOLUTION_SETTING 7500
AC$MASS_SPECTROMETRY: SPRAY_VOLTAGE 4.5 kV
AC$MASS_SPECTROMETRY: TUBE_LENS_VOLTAGE 140 V
AC$CHROMATOGRAPHY: COLUMN_NAME Symmetry C18 Column, Waters
AC$CHROMATOGRAPHY: FLOW_GRADIENT 0min:5%, 24min:95%, 28min:95%, 28.1:5% (acetonitrile)
AC$CHROMATOGRAPHY: FLOW_RATE 0.3 ml/min
AC$CHROMATOGRAPHY: RETENTION_TIME 1095.95 s
AC$CHROMATOGRAPHY: SOLVENT A H2O(0.1%HCOOH)
AC$CHROMATOGRAPHY: SOLVENT B CH3CN(0.1%HCOOH)

MS$FOCUSED_ION: PRECURSOR_M/Z 395.14892
MS$FOCUSED_ION: PRECURSOR_TYPE [M+H]+

PK$SPLASH: splash10-03dm-0696000000-cbec904cb2f70ad2fab0
PK$NUM_PEAK: 111
PK$PEAK: m/z int. rel.int.
  105.604996 1217.462036 2
  106.072731 1251.930176 2
  106.367615 1008.141113 1
  110.110977 1135.696167 2
  110.270363 1357.801147 2
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  121.064644 2123.429932 3
  124.050964 1524.726562 2
  128.06163 2409.056396 3
  131.683273 1077.970947 2
  135.043777 1647.381592 2
  136.051041 2365.910156 3
  139.075378 9476.032227 13
  143.083603 2113.727295 3
  147.080414 14198.652344 20
  148.052261 1468.464111 2
  149.023941 1427.172974 2
  149.697601 1133.530884 2
  150.121902 1625.990967 2
  151.075256 4411.341797 6
  155.070892 1295.238525 2
  157.065125 1669.249268 2
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  161.059692 11788.151367 17
  162.063095 1196.591919 2
  163.075912 2707.446289 4
  167.070221 26159.632812 37
  169.065872 1594.009644 2
  170.072266 5683.137695 8
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  173.059784 1556.967041 2
  175.074814 6698.269531 9
  176.046921 11955.319336 17
  177.054703 18201.525391 26
  178.062653 7975.364746 11
  179.070267 82060.515625 116
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  181.049835 2986.328613 4
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  189.091202 115028.414062 163
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  195.080475 78019.25 111
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  241.510315 1517.841431 2
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  318.922302 1078.657837 2
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  327.086426 26867.5 38
  335.128571 9729.219727 14
  336.13623 8921.984375 13
  339.159912 3518.238525 5
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  349.142975 3314.362793 5
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  364.131348 5272.727051 7
  365.139709 2593.661377 4
  366.845673 1601.745117 2
  367.154205 286800.71875 407
  368.156311 3488.530762 5
  377.138397 31239.173828 44
  380.125732 30571.099609 43
  381.709686 1191.217407 2
  395.148956 191582.625 272
  395.266571 1589.992065 2
  395.824524 1270.7854 2
  396.152161 323454.34375 459
  396.492554 1405.319702 2
  397.040741 1410.949951 2
  407.411133 1374.254272 2
//

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