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MassBank Record: MSBNK-RIKEN-PR300554

Harmalol; LC-ESI-QTOF; MS2

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

ACCESSION: MSBNK-RIKEN-PR300554
RECORD_TITLE: Harmalol; LC-ESI-QTOF; MS2
DATE: 2019.03.28
AUTHORS: Tetsuya Mori, Center for Sustainable Resource Science, RIKEN
LICENSE: CC BY-NC-SA
PUBLICATION: Tsugawa H., Nakabayashi R., Mori T., Yamada Y., Takahashi M., Rai A., Sugiyama R., Yamamoto H., Nakaya T., Yamazaki M., Kooke R., Bac-Molenaar JA., Oztolan-Erol N., Keurentjes JJB., Arita M., Saito K. (2019) "A cheminformatics approach to characterize metabolomes in stable-isotope-labeled organisms" Nature Methods 16(4):295-298. [doi:10.1038/s41592-019-0358-2]
COMMENT: registered in RIKEN PlaSMA

CH$NAME: Harmalol
CH$COMPOUND_CLASS: Harmala alkaloids
CH$FORMULA: C12H12N2O
CH$EXACT_MASS: 200.241
CH$SMILES: CC1=C2NC3=CC(=O)C=CC3=C2CCN1
CH$IUPAC: InChI=1S/C12H12N2O/c1-7-12-10(4-5-13-7)9-3-2-8(15)6-11(9)14-12/h2-3,6,13-14H,4-5H2,1H3
CH$LINK: INCHIKEY CRQDWQWZCNKKAC-UHFFFAOYSA-N

AC$INSTRUMENT: LC, Waters Acquity UPLC System; MS, Waters Xevo G2 Q-Tof
AC$INSTRUMENT_TYPE: LC-ESI-QTOF
AC$MASS_SPECTROMETRY: MS_TYPE MS2
AC$MASS_SPECTROMETRY: ION_MODE POSITIVE
AC$MASS_SPECTROMETRY: COLLISION_ENERGY 6V
AC$MASS_SPECTROMETRY: DESOLVATION_GAS_FLOW 800/h
AC$MASS_SPECTROMETRY: DESOLVATION_TEMPERATURE 450 C
AC$MASS_SPECTROMETRY: IONIZATION ESI
AC$CHROMATOGRAPHY: CAPILLARY_VOLTAGE +3.00 kV
AC$CHROMATOGRAPHY: COLUMN_NAME Acquity bridged ethyl hybrid C18 (1.7 um, 2.1 mm * 100 mm, Waters)
AC$CHROMATOGRAPHY: COLUMN_TEMPERATURE 40 C
AC$CHROMATOGRAPHY: FLOW_GRADIENT A/B = (99.5%/0.5% at 0 min, 99.5%/0.5% at 0.1 min, 20%/80% at 10 min, 0.5%/99.5% at 10.1 min, 0.5%/99.5% at 12.0 min, 99.5%/0.5% at 12.1 min, 99.5%/0.5% at 15.0 min)
AC$CHROMATOGRAPHY: FLOW_RATE 0.3 ml/min at 0 min, 0.3 ml/min at 10 min, 0.4 ml/min at 10.1 min, 0.4 ml/min at 14.4 min, 0.3 ml/min at 14.5 min
AC$CHROMATOGRAPHY: RETENTION_TIME 3.0593
AC$CHROMATOGRAPHY: SOLVENT A water including 0.1% formic acid
AC$CHROMATOGRAPHY: SOLVENT B acetonitrile including 0.1% formic acid

MS$FOCUSED_ION: PRECURSOR_TYPE [M+H]+
MS$FOCUSED_ION: PRECURSOR_M/Z 201.1022395

PK$SPLASH: splash10-03di-0900000000-8a13aa6e4078fd3b7b7d
PK$NUM_PEAK: 89
PK$PEAK: m/z int. rel.int.
  68.05116 112.0 112
  80.01497 7.0 7
  91.05278 27.0 27
  92.05676 6.0 6
  103.05301 7.0 7
  105.07108 19.0 19
  115.05365 108.0 108
  116.05566 37.0 37
  117.05737 148.0 148
  117.07019 10.0 10
  117.38478 13.0 13
  118.05283 6.0 6
  118.06238 18.0 18
  118.07131 9.0 9
  119.04628 7.0 7
  128.04729 8.0 8
  128.06035 23.0 23
  128.07271 7.0 7
  129.06976 37.0 37
  130.06157 15.0 15
  130.07027 34.0 34
  131.01888 15.0 15
  131.04886 24.0 24
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  131.07278 25.0 25
  132.0556 11.0 11
  132.08029 132.0 132
  133.04616 11.0 11
  133.05371 19.0 19
  133.06294 26.0 26
  133.0757 5.0 5
  133.08331 10.0 10
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  139.05862 10.0 10
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  142.06541 25.0 25
  143.0407 5.0 5
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  146.05844 37.0 37
  154.05905 14.0 14
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  156.0845 42.0 42
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  158.06073 94.0 94
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  160.07565 1000.0 999
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  165.05969 6.0 6
  166.04596 5.0 5
  166.06525 40.0 40
  167.06929 27.0 27
  167.07704 10.0 10
  169.04054 9.0 9
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  169.07811 17.0 17
  171.05855 5.0 5
  172.0831 12.0 12
  174.0992 18.0 18
  182.062 7.0 7
  183.06277 81.0 81
  183.07233 44.0 44
  183.08617 6.0 6
  184.0769 150.0 150
  185.07184 151.0 151
  185.87663 5.0 5
  186.0607 9.0 9
  186.08 132.0 132
  187.08662 25.0 25
  199.08701 23.0 23
  200.09311 9.0 9
  200.10716 5.0 5
  201.08215 6.0 6
  201.10374 183.0 183
//

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