MassBank Record: PR300905



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

ACCESSION: PR300905
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$CHROMATOGRAPHY: RETENTION_TIME 4.533533 AC$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: splash10-000i-0930000000-e699dc174b2a6d818ef6 PK$NUM_PEAK: 52 PK$PEAK: m/z int. rel.int. 77.03917 7.0 7 79.05424 6.0 6 103.05276 15.0 15 103.0582 6.0 6 118.06979 8.0 8 131.05099 9.0 9 135.04466 39.0 39 152.06656 7.0 7 159.04752 10.0 10 160.07368 8.0 8 163.03926 24.0 24 163.0565 11.0 11 165.07097 11.0 11 177.06969 32.0 32 178.06259 6.0 6 178.07838 56.0 56 179.07246 13.0 13 179.08591 26.0 26 179.0976 6.0 6 180.09113 12.0 12 187.05655 9.0 9 188.05923 9.0 9 188.06895 23.0 23 189.04034 6.0 6 189.07089 1000.0 999 190.06795 72.0 72 190.07629 182.0 182 191.08372 44.0 44 192.09117 5.0 5 201.06741 13.0 13 202.0811 7.0 7 205.06084 16.0 16 205.06964 14.0 14 207.07349 9.0 9 207.08318 34.0 34 217.06706 160.0 160 218.0656 26.0 26 218.07805 20.0 20 219.06827 6.0 6 219.07997 10.0 10 219.08881 5.0 5 220.08569 7.0 7 221.06261 6.0 6 235.07124 15.0 15 237.09077 17.0 17 246.07137 36.0 36 247.07651 151.0 151 248.08038 22.0 22 275.06921 29.0 29 275.082 17.0 17 276.06534 8.0 8 276.08588 5.0 5 //

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