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MassBank Record: PR310493

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

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

ACCESSION: PR310493
RECORD_TITLE: (-)-Epicatechin; 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: Annotation level-1

CH$NAME: (-)-Epicatechin
CH$COMPOUND_CLASS: Flavanol O-glycosides
CH$FORMULA: C15H14O6
CH$EXACT_MASS: 290.271
CH$SMILES: OC1CC2=C(OC1C1=CC(O)=C(O)C=C1)C=C(O)C=C2O
CH$IUPAC: InChI=1S/C15H14O6/c16-8-4-11(18)9-6-13(20)15(21-14(9)5-8)7-1-2-10(17)12(19)3-7/h1-5,13,15-20H,6H2
CH$LINK: INCHIKEY PFTAWBLQPZVEMU-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 3.43
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 291.08631

PK$SPLASH: splash10-000i-0910000000-d9c8fc86fedc95f5b670
PK$NUM_PEAK: 38
PK$PEAK: m/z int. rel.int.
  68.99197 20.0 21
  77.0418 27.0 28
  99.0428 19.0 20
  105.0378 24.0 25
  111.04939 38.0 40
  112.04723 23.0 24
  115.04118 26.0 27
  119.04675 46.0 48
  120.04819 26.0 27
  123.04376 470.0 495
  124.02526 40.0 42
  124.0459 35.0 37
  124.05338 36.0 38
  127.03778 27.0 28
  139.03999 948.0 999
  140.00023 17.0 18
  140.04318 86.0 91
  141.04126 39.0 41
  143.04813 47.0 50
  147.04494 21.0 22
  151.03842 64.0 67
  151.07314 47.0 50
  159.03807 28.0 30
  163.03749 43.0 45
  165.05553 134.0 141
  179.07957 24.0 25
  180.07701 27.0 28
  181.04541 25.0 26
  189.04794 25.0 26
  207.04332 31.0 33
  207.06032 23.0 24
  207.07407 55.0 58
  244.06752 42.0 44
  249.07143 26.0 27
  273.06647 30.0 32
  273.08081 18.0 19
  291.08197 228.0 240
  291.09534 55.0 58
//

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