MassBank Record: MSBNK-RIKEN-PR300472
ACCESSION: MSBNK-RIKEN-PR300472
RECORD_TITLE: Emetine; 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$NAME: Emetine
CH$COMPOUND_CLASS: Emetine alkaloids
CH$FORMULA: C29H40N2O4
CH$EXACT_MASS: 480.649
CH$SMILES: CC[C@H]1CN2CCC3=CC(OC)=C(OC)C=C3[C@@H]2C[C@@H]1C[C@H]1NCCC2=CC(OC)=C(OC)C=C12
CH$IUPAC: InChI=1S/C29H40N2O4/c1-6-18-17-31-10-8-20-14-27(33-3)29(35-5)16-23(20)25(31)12-21(18)11-24-22-15-28(34-4)26(32-2)13-19(22)7-9-30-24/h13-16,18,21,24-25,30H,6-12,17H2,1-5H3/t18-,21-,24+,25-/m0/s1
CH$LINK: INCHIKEY
AUVVAXYIELKVAI-CKBKHPSWSA-N
AC$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$CHROMATOGRAPHY: RETENTION_TIME 3.412183
AC$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$FOCUSED_ION: PRECURSOR_M/Z 481.3060842
PK$SPLASH: splash10-001i-0130900000-ce45a3d6d6ff62a83a6c
PK$NUM_PEAK: 49
PK$PEAK: m/z int. rel.int.
160.08896 9.0 9
165.09207 47.0 47
177.09109 16.0 16
179.0972 5.0 5
179.11414 13.0 13
191.10545 20.0 20
192.10127 19.0 19
192.11057 17.0 17
194.12151 28.0 28
201.09669 5.0 5
205.10748 5.0 5
206.11543 24.0 24
206.12877 7.0 7
214.10866 7.0 7
220.12875 6.0 6
220.13974 9.0 9
230.12263 6.0 6
231.12405 10.0 10
242.10341 8.0 8
242.15642 6.0 6
244.1313 5.0 5
245.15601 8.0 8
246.14745 149.0 149
247.14516 6.0 6
247.15529 9.0 9
248.13808 6.0 6
256.1796 5.0 5
257.15131 12.0 12
272.16669 37.0 37
273.17944 5.0 5
274.13376 7.0 7
274.17825 60.0 60
274.19644 6.0 6
275.17621 7.0 7
300.20016 14.0 14
337.69516 6.0 6
419.26053 8.0 8
436.25497 7.0 7
462.2608 7.0 7
464.28183 36.0 36
464.31717 6.0 6
465.2803 10.0 10
466.29654 5.0 5
479.27039 12.0 12
479.3017 26.0 26
480.2955 25.0 25
481.24579 6.0 6
481.26932 25.0 25
481.30792 1000.0 999
//