MassBank Record: MSBNK-RIKEN_ReSpect-PT110790
ACCESSION: MSBNK-RIKEN_ReSpect-PT110790
RECORD_TITLE: Gluconasturtiin, Gluconasturcin, 2-Phenethylglucosinolate, [[3-phenyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanylpropylidene]amino] hydrogen sulfate; LC-ESI-QTOF; MS2
DATE: 2008.07.28
AUTHORS: Matsuda F, Suzuki M, Sawada Y, Plant Science Center, RIKEN.
LICENSE: CC BY-NC
COPYRIGHT: Copyright(C) 2009 Plant Science Center, RIKEN
COMMENT: Build 1 2009/06/24
COMMENT: Acquisition and generation of the data is financially supported in part by CREST/JST.
CH$NAME: Gluconasturtiin
CH$NAME: Gluconasturcin
CH$NAME: 2-Phenethylglucosinolate
CH$NAME: [[3-phenyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanylpropylidene]amino] hydrogen sulfate
CH$COMPOUND_CLASS: CLASS1 Glucosinolate CLASS2 Aliphatic glucosinolate
CH$FORMULA: C15H21NO9S2
CH$EXACT_MASS: 423.461
CH$SMILES: C1=CC=C(C=C1)CCC(=NOS(=O)(=O)O)SC2C(C(C(C(O2)CO)O)O)O
CH$IUPAC: InChI=1S/C15H21NO9S2/c17-8-10-12(18)13(19)14(20)15(24-10)26-11(16-25-27(21,22)23)7-6-9-4-2-1-3-5-9/h1-5,10,12-15,17-20H,6-8H2,(H,21,22,23)
CH$LINK: CAS
499-30-9
CH$LINK: INCHIKEY
CKIJIGYDFNXSET-UHFFFAOYSA-N
AC$INSTRUMENT: Q-Tof Premier, Waters
AC$INSTRUMENT_TYPE: LC-ESI-QTOF
AC$MASS_SPECTROMETRY: MS_TYPE MS2
AC$MASS_SPECTROMETRY: ION_MODE POSITIVE
AC$MASS_SPECTROMETRY: IONIZATION ESI
AC$MASS_SPECTROMETRY: COLLISION_ENERGY Ramp 5-45 V
AC$MASS_SPECTROMETRY: CAPILLARY_VOLTAGE 3.0 kV
AC$CHROMATOGRAPHY: SOLVENT CH3CN/H2O
MS$FOCUSED_ION: ION_TYPE [M+H]+
MS$FOCUSED_ION: PRECURSOR_M/Z 462.02945
PK$SPLASH: splash10-01pk-8349400000-e3455f54a0f2cc4fe868
PK$NUM_PEAK: 9
PK$PEAK: m/z int. rel.int.
98.9786 41.15 999
158.9997 9.626 234
188.0432 5.33 129
201.0175 4.472 109
246.0497 10.38 252
262.0256 6.418 156
314.9577 3.863 94
382.0781 40.91 993
462.0294 24.35 591
//