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MassBank Record: PR310492

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

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

ACCESSION: PR310492
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 3.44
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$SPLASH: splash10-000i-0910000000-8721f9812c17ad1764f3
PK$NUM_PEAK: 38
PK$PEAK: m/z int. rel.int.
  67.05427 32.0 36
  97.02874 30.0 34
  105.88937 28.0 32
  111.04481 20.0 23
  119.04736 47.0 54
  123.02245 28.0 32
  123.03466 97.0 111
  123.04417 447.0 510
  124.02824 31.0 35
  139.03308 245.0 279
  139.03897 876.0 999
  140.03896 96.0 109
  143.05385 25.0 29
  145.06572 47.0 54
  147.03664 44.0 50
  147.0442 213.0 243
  148.04858 27.0 31
  151.03168 108.0 123
  151.037 40.0 46
  152.04477 18.0 21
  153.04317 23.0 26
  154.07567 22.0 25
  161.05856 85.0 97
  165.04384 26.0 30
  165.05913 108.0 123
  166.06169 40.0 46
  166.2612 18.0 21
  170.05182 25.0 29
  179.05585 29.0 33
  190.05765 21.0 24
  202.11348 19.0 22
  207.06699 65.0 74
  208.06787 24.0 27
  230.4516 22.0 25
  249.0591 27.0 31
  273.08139 80.0 91
  291.05682 25.0 29
  291.08994 347.0 396
//

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