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MassBank Record: PR303617

Bufalin; LC-ESI-QTOF; MS2

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

ACCESSION: PR303617
RECORD_TITLE: Bufalin; 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$NAME: Bufalin
CH$COMPOUND_CLASS: Bufanolides and derivatives
CH$FORMULA: C24H34O4
CH$EXACT_MASS: 386.532
CH$SMILES: C[C@]12CC[C@H]3[C@@H](CC[C@@H]4C[C@@H](O)CC[C@]34C)[C@@]1(O)CC[C@@H]2C1=COC(=O)C=C1
CH$IUPAC: InChI=1S/C24H34O4/c1-22-10-7-17(25)13-16(22)4-5-20-19(22)8-11-23(2)18(9-12-24(20,23)27)15-3-6-21(26)28-14-15/h3,6,14,16-20,25,27H,4-5,7-13H2,1-2H3/t16-,17+,18-,19+,20-,22+,23-,24+/m1/s1
CH$LINK: INCHIKEY QEEBRPGZBVVINN-BMPKRDENSA-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 6.99085
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 387.252986

PK$SPLASH: splash10-000i-0209000000-fe296922687927e4a9d2
PK$NUM_PEAK: 45
PK$PEAK: m/z int. rel.int.
  93.06827 6.0 6
  95.08694 6.0 6
  105.07038 13.0 13
  107.08562 20.0 20
  109.10201 9.0 9
  119.08259 5.0 5
  121.10092 13.0 13
  131.08727 10.0 10
  133.09454 5.0 5
  133.10492 13.0 13
  135.1158 12.0 12
  136.12221 5.0 5
  143.08403 8.0 8
  145.09811 8.0 8
  145.10406 11.0 11
  147.11685 21.0 21
  149.13435 10.0 10
  155.08276 5.0 5
  157.09995 6.0 6
  159.11746 24.0 24
  161.09596 8.0 8
  161.13135 20.0 20
  173.13103 12.0 12
  175.14464 8.0 8
  183.11597 7.0 7
  185.13049 7.0 7
  187.14977 7.0 7
  195.1125 6.0 6
  197.13092 9.0 9
  199.15207 6.0 6
  243.13878 7.0 7
  255.20302 17.0 17
  255.21497 25.0 25
  256.21619 12.0 12
  257.2269 6.0 6
  269.14828 7.0 7
  305.22488 11.0 11
  315.20987 5.0 5
  333.23019 7.0 7
  351.2338 48.0 48
  352.23193 11.0 11
  352.24741 5.0 5
  369.24197 33.0 33
  387.25409 1000.0 999
  387.31137 19.0 19
//

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