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MassBank Record: PR304180

alpha,beta-Dihydroresveratrol; LC-ESI-QTOF; MS2

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

ACCESSION: PR304180
RECORD_TITLE: alpha,beta-Dihydroresveratrol; 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$NAME: alpha,beta-Dihydroresveratrol
CH$COMPOUND_CLASS: Stilbenes
CH$FORMULA: C14H14O3
CH$EXACT_MASS: 230.263
CH$SMILES: OC1=CC=C(CCC2=CC(O)=CC(O)=C2)C=C1
CH$IUPAC: InChI=1S/C14H14O3/c15-12-5-3-10(4-6-12)1-2-11-7-13(16)9-14(17)8-11/h3-9,15-17H,1-2H2
CH$LINK: INCHIKEY HITJFUSPLYBJPE-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 5.145717
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 231.1015708

PK$SPLASH: splash10-0019-0930000000-eb8a1ec39aaee98dd4d4
PK$NUM_PEAK: 50
PK$PEAK: m/z int. rel.int.
  51.02178 7.0 7
  56.01724 14.0 14
  68.99588 8.0 8
  77.02647 7.0 7
  77.03904 16.0 16
  79.04909 8.0 8
  79.05289 7.0 7
  81.07233 9.0 9
  91.05433 70.0 70
  91.06143 15.0 15
  93.03098 10.0 10
  93.07054 29.0 29
  94.03952 8.0 8
  103.05225 8.0 8
  103.0595 20.0 20
  105.74953 8.0 8
  107.04967 492.0 492
  107.88854 9.0 9
  108.0489 42.0 42
  108.05878 8.0 8
  109.04894 8.0 8
  109.06463 21.0 21
  109.0746 7.0 7
  110.06662 19.0 19
  110.19305 8.0 8
  110.94829 13.0 13
  119.04646 8.0 8
  121.03275 8.0 8
  121.04649 8.0 8
  121.06516 490.0 490
  122.06564 38.0 38
  122.07491 33.0 33
  123.04549 7.0 7
  125.06052 52.0 52
  137.05966 1000.0 999
  138.05916 47.0 47
  138.07056 34.0 34
  139.05318 8.0 8
  139.06406 9.0 9
  139.1172 9.0 9
  149.95076 9.0 9
  155.19073 9.0 9
  156.71858 8.0 8
  178.07587 7.0 7
  183.07692 8.0 8
  213.07999 8.0 8
  214.10612 9.0 9
  231.02168 11.0 11
  231.0679 8.0 8
  231.10356 922.0 921
//

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