MassBank Record: MSBNK-RIKEN-PR301557
ACCESSION: MSBNK-RIKEN-PR301557
RECORD_TITLE: Vincamine; 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$NAME: Vincamine
CH$COMPOUND_CLASS: Eburnan-type alkaloids
CH$FORMULA: C21H26N2O3
CH$EXACT_MASS: 354.45
CH$SMILES: CCC12CCCN3CCC4=C(C13)N(C1=CC=CC=C41)C(O)(C2)C(=O)OC
CH$IUPAC: InChI=1S/C21H26N2O3/c1-3-20-10-6-11-22-12-9-15-14-7-4-5-8-16(14)23(17(15)18(20)22)21(25,13-20)19(24)26-2/h4-5,7-8,18,25H,3,6,9-13H2,1-2H3
CH$LINK: INCHIKEY
RXPRRQLKFXBCSJ-UHFFFAOYSA-N
AC$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$CHROMATOGRAPHY: RETENTION_TIME 4.50125
AC$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$FOCUSED_ION: PRECURSOR_M/Z 355.2016192
PK$SPLASH: splash10-0a4i-0039000000-46b5ba08c7ba3c2c1ed4
PK$NUM_PEAK: 43
PK$PEAK: m/z int. rel.int.
144.08081 53.0 53
145.08298 5.0 5
152.10811 19.0 19
194.11929 6.0 6
205.08797 8.0 8
206.09564 11.0 11
208.11174 7.0 7
209.11546 8.0 8
212.12817 30.0 30
220.11263 6.0 6
222.12589 11.0 11
223.13283 5.0 5
224.14526 6.0 6
234.12495 15.0 15
239.09537 6.0 6
248.14265 7.0 7
250.16339 7.0 7
252.10202 9.0 9
253.11131 6.0 6
264.10098 18.0 18
265.11096 28.0 28
266.11615 16.0 16
267.12216 12.0 12
268.13336 26.0 26
277.16528 10.0 10
278.1199 7.0 7
279.12418 12.0 12
280.13333 92.0 92
281.13568 16.0 16
282.14755 6.0 6
292.13431 9.0 9
294.14868 97.0 97
295.14844 13.0 13
295.17975 21.0 21
307.14661 10.0 10
308.16339 67.0 67
309.16614 23.0 23
310.1788 9.0 9
337.19147 336.0 336
338.19437 89.0 89
339.19922 10.0 10
355.20178 1000.0 999
355.25552 29.0 29
//