MassBank MassBank Search Contents Download

MassBank Record: MSBNK-RIKEN-PR308728

Bergenin; LC-ESI-QTOF; MS2

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

ACCESSION: MSBNK-RIKEN-PR308728
RECORD_TITLE: Bergenin; 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: Annotation level-1

CH$NAME: Bergenin
CH$COMPOUND_CLASS: Phenolic glycosides
CH$FORMULA: C14H16O9
CH$EXACT_MASS: 328.273
CH$SMILES: COC1=C(O)C2=C(C=C1O)C(=O)OC1C(O)C(O)C(CO)OC21
CH$IUPAC: InChI=1S/C14H16O9/c1-21-11-5(16)2-4-7(9(11)18)12-13(23-14(4)20)10(19)8(17)6(3-15)22-12/h2,6,8,10,12-13,15-19H,3H2,1H3
CH$LINK: INCHIKEY YWJXCIXBAKGUKZ-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 NEGATIVE
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 2.85
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 327.07216

PK$SPLASH: splash10-054o-0986000000-c765d4b15a8af89d20ca
PK$NUM_PEAK: 76
PK$PEAK: m/z int. rel.int.
  97.28213 23.0 9
  106.0389 18.0 7
  108.02244 18.0 7
  121.0331 21.0 8
  125.02652 24.0 9
  135.03333 20.0 8
  138.03227 79.0 31
  149.01688 21.0 8
  149.02324 76.0 30
  149.03696 24.0 9
  152.03877 26.0 10
  160.0201 21.0 8
  161.02193 139.0 55
  161.02875 91.0 36
  162.02849 67.0 26
  162.04022 41.0 16
  163.03995 26.0 10
  164.00999 173.0 68
  165.01999 62.0 24
  166.02846 136.0 53
  166.04602 19.0 7
  167.02814 22.0 9
  173.0183 33.0 13
  175.99983 18.0 7
  177.02434 33.0 13
  178.0191 86.0 34
  178.034 19.0 7
  179.02831 19.0 7
  179.03949 19.0 7
  181.03732 25.0 10
  181.07964 18.0 7
  183.02539 18.0 7
  189.01974 19.0 7
  190.02444 158.0 62
  190.74722 19.0 7
  191.03598 21.0 8
  192.00636 1276.0 502
  193.01186 628.0 247
  193.05048 18.0 7
  194.01591 387.0 152
  194.02408 446.0 175
  195.02016 19.0 7
  196.02515 43.0 17
  196.04692 24.0 9
  204.98743 21.0 8
  205.01045 154.0 61
  206.02455 116.0 46
  207.02866 1800.0 708
  208.02835 80.0 31
  208.03818 72.0 28
  208.05835 18.0 7
  209.03607 23.0 9
  209.04735 50.0 20
  211.03384 18.0 7
  221.01105 22.0 9
  222.01262 151.0 59
  222.02925 20.0 8
  223.01862 21.0 8
  223.02885 40.0 16
  223.06871 20.0 8
  233.01028 18.0 7
  234.01816 668.0 263
  235.00697 20.0 8
  235.01837 57.0 22
  237.03522 157.0 62
  238.04666 38.0 15
  249.03922 564.0 222
  250.03946 91.0 36
  251.05164 39.0 15
  294.02869 21.0 8
  294.03983 63.0 25
  295.04947 20.0 8
  312.02957 52.0 20
  312.04871 552.0 217
  313.06006 42.0 17
  327.07129 2541.0 999
//

system version 2.2.8
Copyright © 2006 MassBank Project; 2011 NORMAN Association; 2021 MassBank Consortium
de.NBI logo
EAWAG logo
fnr logo
IPB logo
NORMAN logo
UFZ logo
LCSB logo
HBM4EU logo
nfdi4chem logo