MassBank Record: PR301783



 (+)-Chelidonine; LC-ESI-QTOF; MS2 
Mass Spectrum
Chemical Structure
Generated by the Chemistry Development Kit (http://github.com/cdk) \n

ACCESSION: PR301783
RECORD_TITLE: (+)-Chelidonine; LC-ESI-QTOF; MS2
DATE: 2019.03.28
AUTHORS: , Tetsuya Mori, Center for Sustainable Resource Science, RIKEN
LICENSE: CC BY-SA NC
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$NAME: Chelidonin CH$NAME: (+)-Chelidonine CH$NAME: [1,3]Benzodioxolo[5,6-c]-1,3-dioxolo[4,5-i]phenanthridin-6-ol, 5b,6,7,12b,13,14-hexahydro-13-methyl-, (5bR,6S,12bS)- CH$COMPOUND_CLASS: Hexahydrobenzophenanthridine alkaloids CH$FORMULA: C20H19NO5 CH$EXACT_MASS: 353.126323 CH$SMILES: CN1CC2=C(C=CC3=C2OCO3)[C@@H]4[C@H]1C5=CC6=C(C=C5C[C@@H]4O)OCO6 CH$IUPAC: InChI=1S/C20H19NO5/c1-21-7-13-11(2-3-15-20(13)26-9-23-15)18-14(22)4-10-5-16-17(25-8-24-16)6-12(10)19(18)21/h2-3,5-6,14,18-19,22H,4,7-9H2,1H3/t14-,18-,19+/m0/s1 CH$LINK: CAS 476-32-4 CH$LINK: CHEMSPIDER 171216 CH$LINK: COMPTOX DTXSID10878474 CH$LINK: INCHIKEY GHKISGDRQRSCII-ZOCIIQOWSA-N CH$LINK: PUBCHEM CID:197810
AC$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$CHROMATOGRAPHY: RETENTION_TIME 4.5206 AC$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$FOCUSED_ION: PRECURSOR_M/Z 354.1335992
PK$SPLASH: splash10-004j-0190000000-8ec8bc9de6169b32dbb7 PK$NUM_PEAK: 58 PK$PEAK: m/z int. rel.int. 131.05162 6.0 6 135.04521 101.0 101 136.05066 6.0 6 143.05431 11.0 11 159.04745 12.0 12 161.0602 35.0 35 163.03969 81.0 81 164.04799 6.0 6 173.05128 5.0 5 173.06007 13.0 13 176.07887 7.0 7 179.08844 13.0 13 187.03954 9.0 9 188.0726 46.0 46 189.07092 58.0 58 190.07954 15.0 15 207.06918 5.0 5 207.08022 20.0 20 207.08957 8.0 8 217.06885 111.0 111 218.06516 15.0 15 218.07828 14.0 14 219.07054 5.0 5 219.0798 10.0 10 235.07959 38.0 38 237.09238 55.0 55 238.10094 9.0 9 245.06068 26.0 26 246.04985 6.0 6 246.06943 15.0 15 247.02859 7.0 7 247.07843 527.0 526 248.08163 104.0 104 249.08572 7.0 7 249.09612 8.0 8 263.07205 11.0 11 264.07935 5.0 5 265.08737 57.0 57 266.08276 8.0 8 266.09683 14.0 14 275.07272 1000.0 999 276.07553 224.0 224 277.07281 19.0 19 277.08502 20.0 20 278.05862 5.0 5 293.07285 13.0 13 293.08731 17.0 17 295.09189 19.0 19 295.10703 23.0 23 296.10147 6.0 6 305.07648 28.0 28 305.09464 13.0 13 306.08386 9.0 9 323.08481 12.0 12 323.10196 20.0 20 336.11206 9.0 9 336.12469 16.0 16 337.13126 5.0 5 //

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