MassBank Record: PB005864



 Laudanosine; LC-ESI-QTOF; MS2; CE:10 eV; [M+H]+ 
Mass Spectrum
Chemical Structure
Generated by the Chemistry Development Kit (http://github.com/cdk) \n

ACCESSION: PB005864
RECORD_TITLE: Laudanosine; LC-ESI-QTOF; MS2; CE:10 eV; [M+H]+
DATE: 2016.01.19 (Created 2009.02.20, modified 2013.06.04)
AUTHORS: Heinz T, Institute of Plant Biochemistry, Halle, Germany
LICENSE: CC BY-SA
COMMENT: IPB_RECORD: 2441
COMMENT: CONFIDENCE: confident structure

CH$NAME: Laudanosine CH$NAME: 1-[(3,4-dimethoxyphenyl)methyl]-6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinoline CH$COMPOUND_CLASS: Natural Product CH$FORMULA: C21H27NO4 CH$EXACT_MASS: 357.19401 CH$SMILES: CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)OC)OC)OC CH$IUPAC: InChI=1S/C21H27NO4/c1-22-9-8-15-12-20(25-4)21(26-5)13-16(15)17(22)10-14-6-7-18(23-2)19(11-14)24-3/h6-7,11-13,17H,8-10H2,1-5H3 CH$LINK: INCHIKEY KGPAYJZAMGEDIQ-UHFFFAOYSA-N CH$LINK: PUBCHEM CID:15548
AC$INSTRUMENT: micrOTOF-Q AC$INSTRUMENT_TYPE: LC-ESI-QTOF AC$MASS_SPECTROMETRY: MS_TYPE MS2 AC$MASS_SPECTROMETRY: ION_MODE POSITIVE AC$MASS_SPECTROMETRY: COLLISION_ENERGY 10 eV AC$MASS_SPECTROMETRY: IONIZATION ESI
MS$FOCUSED_ION: PRECURSOR_TYPE [M+H]+
PK$SPLASH: splash10-0a4i-0019000000-13cd7882f0de25fc26b2 PK$NUM_PEAK: 13 PK$PEAK: m/z int. rel.int. 151.074 10.020 0 189.089 30.060 2 206.115 1993.988 198 207.119 180.361 17 296.136 10.020 0 315.154 40.080 3 327.155 240.481 23 328.158 30.060 2 329.170 10.020 0 357.914 10.020 0 358.197 10000.000 999 359.200 1603.206 159 360.202 40.080 3 //