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MassBank Record: MSBNK-RIKEN-PR304358

Saikosaponin D; LC-ESI-QTOF; MS2

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

ACCESSION: MSBNK-RIKEN-PR304358
RECORD_TITLE: Saikosaponin D; 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$NAME: Saikosaponin D
CH$COMPOUND_CLASS: Triterpene saponins
CH$FORMULA: C42H68O13
CH$EXACT_MASS: 780.993
CH$SMILES: C[C@H]1O[C@@H](O[C@H]2CC[C@@]3(C)[C@@H](CC[C@]4(C)[C@@H]3C=CC35OC[C@@]6(CCC(C)(C)CC36)C(O)C[C@@]45C)[C@]2(C)CO)[C@H](O)C(OC2OC(CO)C(O)C(O)[C@H]2O)C1O
CH$IUPAC: InChI=1S/C42H68O13/c1-21-28(46)33(55-34-31(49)30(48)29(47)22(18-43)53-34)32(50)35(52-21)54-27-10-11-37(4)23(38(27,5)19-44)8-12-39(6)24(37)9-13-42-25-16-36(2,3)14-15-41(25,20-51-42)26(45)17-40(39,42)7/h9,13,21-35,43-50H,8,10-12,14-20H2,1-7H3/t21-,22?,23-,24-,25?,26?,27+,28?,29?,30?,31-,32-,33?,34?,35+,37+,38+,39-,40+,41-,42?/m1/s1
CH$LINK: INCHIKEY KYWSCMDFVARMPN-DISCDMJRSA-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 8.253117
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 781.4732687

PK$SPLASH: splash10-0a4i-0131900000-4377c326628443adf24b
PK$NUM_PEAK: 88
PK$PEAK: m/z int. rel.int.
  75.04473 39.0 39
  111.04245 39.0 39
  122.10857 39.0 39
  147.07021 39.0 39
  151.11047 47.0 47
  163.14619 42.0 42
  169.1033 52.0 52
  185.13545 54.0 54
  187.13002 81.0 81
  187.14828 42.0 42
  189.13692 49.0 49
  193.16986 39.0 39
  204.18138 39.0 39
  205.16788 79.0 79
  211.14772 49.0 49
  215.18367 133.0 133
  217.14699 39.0 39
  217.19617 52.0 52
  219.18103 59.0 59
  223.16476 39.0 39
  225.16867 39.0 39
  227.16293 42.0 42
  232.19801 62.0 62
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  239.18275 42.0 42
  240.18683 42.0 42
  241.20305 57.0 57
  243.18359 39.0 39
  246.18935 47.0 47
  247.16339 39.0 39
  249.18999 52.0 52
  251.18576 94.0 94
  254.05989 59.0 59
  267.19287 44.0 44
  267.21057 79.0 79
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  377.28525 39.0 39
  379.31488 39.0 39
  389.3172 135.0 135
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  408.34546 39.0 39
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  420.32471 42.0 42
  421.26086 49.0 49
  425.32367 39.0 39
  425.34677 261.0 261
  426.32004 39.0 39
  426.35919 111.0 111
  428.93979 74.0 74
  436.12317 57.0 57
  437.33551 355.0 355
  438.29779 52.0 52
  438.3237 62.0 62
  438.3504 99.0 99
  439.35568 39.0 39
  455.32883 421.0 421
  455.35175 1000.0 999
  455.37317 236.0 236
  455.58273 49.0 49
  456.35886 362.0 362
  457.36221 42.0 42
  473.36353 47.0 47
  473.38394 49.0 49
  512.35229 47.0 47
  569.36383 49.0 49
  600.40015 52.0 52
  601.37238 57.0 57
  601.40082 49.0 49
  763.46967 52.0 52
  764.4538 39.0 39
//

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