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MassBank Record: PR301511

(-)-Eburnamonine; LC-ESI-QTOF; MS2

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

ACCESSION: PR301511
RECORD_TITLE: (-)-Eburnamonine; LC-ESI-QTOF; MS2
DATE: 2019.03.28
AUTHORS: Tetsuya Mori, Center for Sustainable Resource Science, RIKEN
LICENSE: CC BY-SA NC
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$NAME: (-)-Eburnamonine
CH$COMPOUND_CLASS: Eburnan-type alkaloids
CH$FORMULA: C19H22N2O
CH$EXACT_MASS: 294.398
CH$SMILES: CCC12CCCN3CCC4=C(C13)N(C1=CC=CC=C41)C(=O)C2
CH$IUPAC: InChI=1S/C19H22N2O/c1-2-19-9-5-10-20-11-8-14-13-6-3-4-7-15(13)21(16(22)12-19)17(14)18(19)20/h3-4,6-7,18H,2,5,8-12H2,1H3
CH$LINK: INCHIKEY WYJAPUKIYAZSEM-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 4.648283
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 295.1804898

PK$SPLASH: splash10-0002-0090000000-453e901cb94dc0a0c925
PK$NUM_PEAK: 41
PK$PEAK: m/z int. rel.int.
  70.06712 6.0 6
  84.08179 11.0 11
  144.08174 18.0 18
  152.10687 12.0 12
  168.08017 10.0 10
  180.08044 7.0 7
  181.08722 9.0 9
  194.09529 9.0 9
  195.10445 10.0 10
  196.07599 13.0 13
  197.08238 21.0 21
  208.11424 7.0 7
  209.11725 6.0 6
  210.09369 12.0 12
  210.1274 9.0 9
  211.09378 5.0 5
  222.09291 12.0 12
  223.09906 28.0 28
  224.10666 13.0 13
  224.12534 10.0 10
  224.13945 9.0 9
  225.11258 11.0 11
  226.12383 21.0 21
  227.12766 7.0 7
  235.09998 11.0 11
  236.14156 6.0 6
  237.11493 12.0 12
  238.12184 92.0 92
  238.15765 6.0 6
  239.12711 24.0 24
  249.11487 12.0 12
  252.13747 31.0 31
  253.14139 7.0 7
  253.16446 19.0 19
  253.1761 13.0 13
  254.17365 6.0 6
  264.13861 21.0 21
  266.15402 58.0 58
  267.15723 17.0 17
  295.18109 1000.0 999
  295.23007 32.0 32
//

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