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MassBank Record: MSBNK-RIKEN-PR304044

Luteolinidin; LC-ESI-QTOF; MS2

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

ACCESSION: MSBNK-RIKEN-PR304044
RECORD_TITLE: Luteolinidin; 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: registered in RIKEN PlaSMA

CH$NAME: Luteolinidin
CH$COMPOUND_CLASS: 7-hydroxyflavonoids
CH$FORMULA: C15H10O5
CH$EXACT_MASS: 270.24
CH$SMILES: OC1=CC(O)=C2C=CC(=[O+]C2=C1)C1=CC([O-])=C(O)C=C1
CH$IUPAC: InChI=1S/C15H10O5/c16-9-6-12(18)10-2-4-14(20-15(10)7-9)8-1-3-11(17)13(19)5-8/h1-7H,(H3-,16,17,18,19)
CH$LINK: INCHIKEY GDNIGMNXEKGFIP-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 3.598017
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 271.0600999

PK$SPLASH: splash10-014i-0900000000-15995df0adde8549caab
PK$NUM_PEAK: 86
PK$PEAK: m/z int. rel.int.
  68.9907 21.0 21
  68.99925 42.0 42
  77.03933 44.0 44
  79.01891 19.0 19
  81.03382 38.0 38
  83.0223 21.0 21
  87.02213 28.0 28
  89.04011 81.0 81
  91.05412 19.0 19
  92.05638 22.0 22
  101.03803 31.0 31
  102.04726 39.0 39
  103.04807 32.0 32
  104.05598 18.0 18
  109.02566 55.0 55
  109.03265 82.0 82
  110.03255 19.0 19
  113.03677 84.0 84
  113.04517 19.0 19
  114.04529 37.0 37
  114.0557 31.0 31
  115.04182 20.0 20
  115.0553 1000.0 999
  115.13392 18.0 18
  116.06008 77.0 77
  121.03046 22.0 22
  122.03091 21.0 21
  125.03888 21.0 21
  126.03715 27.0 27
  126.0477 21.0 21
  127.01422 22.0 22
  127.05318 282.0 282
  128.05511 70.0 70
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  139.06236 34.0 34
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  140.05852 24.0 24
  140.06584 64.0 64
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  141.06972 52.0 52
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  141.89519 18.0 18
  142.02443 18.0 18
  142.07564 18.0 18
  142.08536 26.0 26
  145.05771 19.0 19
  147.04111 47.0 47
  147.05347 29.0 29
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  151.01514 23.0 23
  151.04785 58.0 58
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  152.07262 19.0 19
  153.06737 31.0 31
  153.37747 18.0 18
  154.04759 35.0 35
  155.04466 112.0 112
  155.05844 39.0 39
  158.06885 19.0 19
  159.02798 60.0 60
  159.04538 128.0 128
  162.04449 18.0 18
  163.02042 20.0 20
  165.02563 23.0 23
  168.04347 20.0 20
  168.05397 48.0 48
  168.05919 22.0 22
  169.06628 38.0 38
  171.05421 32.0 32
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  184.04877 26.0 26
  187.05264 19.0 19
  188.04878 19.0 19
  197.04436 20.0 20
  215.05156 18.0 18
  224.03867 19.0 19
  242.0621 18.0 18
  271.05087 30.0 30
//

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