MassBank Record: MSBNK-RIKEN-PR302201
ACCESSION: MSBNK-RIKEN-PR302201
RECORD_TITLE: Daidzein-8-C-glucoside; 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$NAME: Daidzein-8-C-glucoside
CH$COMPOUND_CLASS: Isoflavonoid C-glycosides
CH$FORMULA: C21H20O9
CH$EXACT_MASS: 416.382
CH$SMILES: OC[C@H]1O[C@H]([C@H](O)[C@@H](O)[C@@H]1O)C1=C(O)C=CC2=C1OC=C(C2=O)C1=CC=C(O)C=C1
CH$IUPAC: InChI=1S/C21H20O9/c22-7-14-17(26)18(27)19(28)21(30-14)15-13(24)6-5-11-16(25)12(8-29-20(11)15)9-1-3-10(23)4-2-9/h1-6,8,14,17-19,21-24,26-28H,7H2/t14-,17-,18+,19-,21+/m1/s1
CH$LINK: INCHIKEY
HKEAFJYKMMKDOR-VPRICQMDSA-N
AC$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$CHROMATOGRAPHY: RETENTION_TIME 3.274983
AC$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$FOCUSED_ION: PRECURSOR_M/Z 417.1180087
PK$SPLASH: splash10-00kb-0095000000-f2d5e9c37feb8afb11a5
PK$NUM_PEAK: 101
PK$PEAK: m/z int. rel.int.
107.0509 8.0 8
109.02659 6.0 6
135.04222 7.0 7
161.01978 5.0 5
175.03392 12.0 12
179.03456 7.0 7
211.08141 6.0 6
223.04333 6.0 6
223.07336 7.0 7
226.05952 5.0 5
237.09767 6.0 6
239.07199 20.0 20
240.07584 18.0 18
241.07957 13.0 13
241.09991 5.0 5
251.11397 8.0 8
253.08263 6.0 6
255.06396 13.0 13
267.02859 8.0 8
267.0647 913.0 912
268.06525 157.0 157
268.07834 118.0 118
269.04306 6.0 6
269.05899 8.0 8
269.07535 57.0 57
269.08777 17.0 17
270.08365 5.0 5
279.05295 38.0 38
279.07083 84.0 84
279.10355 7.0 7
280.06424 7.0 7
281.07056 67.0 67
281.08401 83.0 83
281.09891 18.0 18
282.07733 34.0 34
282.08878 17.0 17
289.08371 9.0 9
291.06387 16.0 16
292.06369 9.0 9
292.08154 16.0 16
293.07983 50.0 50
293.10193 5.0 5
294.07544 16.0 16
295.05939 33.0 33
295.09003 9.0 9
297.02127 13.0 13
297.04288 15.0 15
297.0751 1000.0 999
298.07666 229.0 229
299.0885 10.0 10
305.09525 8.0 8
307.05591 16.0 16
307.09085 205.0 205
307.10309 185.0 185
307.12152 15.0 15
308.0473 6.0 6
308.06097 5.0 5
308.09836 71.0 71
309.04941 11.0 11
309.07614 41.0 41
309.09698 19.0 19
309.10944 10.0 10
310.07904 8.0 8
310.09601 10.0 10
311.08838 20.0 20
317.07965 7.0 7
321.02924 7.0 7
321.07623 336.0 336
322.07269 41.0 41
322.08475 39.0 39
323.09695 8.0 8
327.07874 8.0 8
327.09207 20.0 20
328.06607 6.0 6
328.0871 6.0 6
333.07623 16.0 16
333.09088 5.0 5
334.07126 7.0 7
335.07852 32.0 32
335.09479 75.0 75
336.09091 12.0 12
339.0578 7.0 7
339.07971 19.0 19
339.10681 7.0 7
340.08368 5.0 5
345.08334 18.0 18
351.08307 109.0 109
352.09088 19.0 19
363.05014 7.0 7
363.07953 121.0 121
363.09381 57.0 57
364.08743 15.0 15
364.10449 20.0 20
381.07187 7.0 7
381.09863 70.0 70
381.1156 33.0 33
382.10123 28.0 28
383.10126 10.0 10
399.09457 10.0 10
399.11725 6.0 6
417.14001 6.0 6
//