MassBank Record: MSBNK-RIKEN-PR300231
ACCESSION: MSBNK-RIKEN-PR300231
RECORD_TITLE: Rhynchophylline; 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$NAME: Rhynchophylline
CH$COMPOUND_CLASS: Indolizidines
CH$FORMULA: C22H28N2O4
CH$EXACT_MASS: 384.476
CH$SMILES: CC[C@H]1CN2CC[C@@]3([C@@H]2C[C@@H]1\C(=C/OC)C(=O)OC)C(O)=NC1=CC=CC=C31
CH$IUPAC: InChI=1S/C22H28N2O4/c1-4-14-12-24-10-9-22(17-7-5-6-8-18(17)23-21(22)26)19(24)11-15(14)16(13-27-2)20(25)28-3/h5-8,13-15,19H,4,9-12H2,1-3H3,(H,23,26)/b16-13+/t14-,15-,19-,22+/m0/s1
CH$LINK: INCHIKEY
DAXYUDFNWXHGBE-KAXDATADSA-N
AC$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$CHROMATOGRAPHY: RETENTION_TIME 4.901633
AC$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$FOCUSED_ION: PRECURSOR_M/Z 385.2121838
PK$SPLASH: splash10-03di-0952000000-d3687810b8859864b2a7
PK$NUM_PEAK: 71
PK$PEAK: m/z int. rel.int.
56.04938 9.0 9
70.06602 51.0 51
71.06995 6.0 6
93.07178 16.0 16
108.08031 43.0 43
110.08313 5.0 5
110.09612 175.0 175
111.09945 12.0 12
115.05536 5.0 5
118.06727 15.0 15
124.11407 19.0 19
129.05585 53.0 53
130.06512 5.0 5
132.04395 29.0 29
132.08128 74.0 74
133.08104 7.0 7
139.07553 22.0 22
142.06552 61.0 61
143.06047 5.0 5
144.07964 80.0 80
145.0867 11.0 11
153.09084 14.0 14
158.05544 19.0 19
158.06114 37.0 37
158.09538 19.0 19
159.06281 7.0 7
160.07587 1000.0 999
160.11357 11.0 11
161.07887 109.0 109
162.0843 5.0 5
162.093 7.0 7
166.0889 6.0 6
168.10362 16.0 16
171.10213 86.0 86
172.07658 30.0 30
172.10561 11.0 11
173.08325 6.0 6
186.09036 9.0 9
187.08588 8.0 8
187.12358 9.0 9
194.11726 40.0 40
195.11946 5.0 5
213.10452 54.0 54
214.10266 15.0 15
215.11978 175.0 175
216.11966 15.0 15
226.14452 130.0 130
227.14934 14.0 14
240.15724 18.0 18
241.13516 50.0 50
251.11839 9.0 9
265.13602 79.0 79
266.14206 14.0 14
267.14871 95.0 95
267.15799 39.0 39
268.1579 17.0 17
269.12094 5.0 5
269.14212 5.0 5
269.16531 362.0 362
270.16714 67.0 67
281.13052 12.0 12
321.1474 7.0 7
321.16095 16.0 16
321.17322 6.0 6
353.18701 192.0 192
354.16046 9.0 9
354.17999 19.0 19
354.19531 43.0 43
355.18689 7.0 7
383.19693 12.0 12
385.21301 379.0 379
//