MassBank MassBank Search Contents Download

MassBank Record: MSBNK-BAFG-CSL23111010385

Omeprazole sulfide 5-carboxylic acid; LC-ESI-QTOF; MS2; 120 V

Mass Spectrum
Chemical Structure
Generated by the Chemistry Development Kit (http://github.com/cdk)

ACCESSION: MSBNK-BAFG-CSL23111010385
RECORD_TITLE: Omeprazole sulfide 5-carboxylic acid; LC-ESI-QTOF; MS2; 120 V
DATE: 2023.11.10
AUTHORS: Kevin S. Jewell; Björn Ehlig; Arne Wick
LICENSE: dl-de/by-2-0
COPYRIGHT: Copyright 2023 Federal Institute of Hydrology, Koblenz, Germany
COMMENT: CONFIDENCE Reference Standard (Level 1)
COMMENT: Chromatography method: dx.doi.org/10.1016/j.chroma.2015.11.014
COMMENT: Acquisition method: 10.1002/rcm.8541

CH$NAME: Omeprazole sulfide 5-carboxylic acid
CH$COMPOUND_CLASS: Metabolite; Pharmaceutical
CH$FORMULA: C17H17N3O4S
CH$EXACT_MASS: 359.094
CH$SMILES: CC1=C(C(=CN=C1CSC2=NC3=C(N2)C=C(C=C3)OC)C(=O)O)OC
CH$IUPAC: InChI=1S/C17H17N3O4S/c1-9-14(18-7-11(16(21)22)15(9)24-3)8-25-17-19-12-5-4-10(23-2)6-13(12)20-17/h4-7H,8H2,1-3H3,(H,19,20)(H,21,22)
CH$LINK: CAS 103877-00-5
CH$LINK: INCHIKEY BNOSHBGSJBEMGC-UHFFFAOYSA-N

AC$INSTRUMENT: TripleTOF 5600 SCIEX
AC$INSTRUMENT_TYPE: LC-ESI-QTOF
AC$MASS_SPECTROMETRY: MS_TYPE MS2
AC$MASS_SPECTROMETRY: ION_MODE POSITIVE
AC$MASS_SPECTROMETRY: COLLISION_ENERGY 120
AC$MASS_SPECTROMETRY: FRAGMENTATION_MODE CID
AC$MASS_SPECTROMETRY: IONIZATION ESI
AC$CHROMATOGRAPHY: COLUMN_NAME Zorbax Eclipse Plus C18 2.1 mm x 150 mm, 3.5 um, Agilent
AC$CHROMATOGRAPHY: COLUMN_TEMPERATURE 40 °C
AC$CHROMATOGRAPHY: FLOW_GRADIENT 0 min min 98% A, 1 min 98% A, 2 min 80% A, 16.5 min 2% A, 22 min 2% A, 22.1 min 98% A, 27 min 98% A
AC$CHROMATOGRAPHY: FLOW_RATE 0.3 mL/min
AC$CHROMATOGRAPHY: RETENTION_TIME 5.75 min
AC$CHROMATOGRAPHY: SOLVENT A: Water 0.1% Formic acid, B: Acetonitrile 0.1% Formic acid

MS$FOCUSED_ION: PRECURSOR_M/Z 360.1013
MS$FOCUSED_ION: PRECURSOR_TYPE [M+H]+
MS$DATA_PROCESSING: COMMENT Export with Spectra 1.9.12 MsBackendMassbank 1.7.4
MS$DATA_PROCESSING: WHOLE RMassBank 2.3.1

PK$SPLASH: splash10-056r-9500000000-d6dd4becf17f43f62329
PK$NUM_PEAK: 81
PK$PEAK: m/z int. rel.int.
  42.0452 2.7 66
  43.0302 2.6 63
  50.024 2 49
  51.0324 6.3 154
  52.0385 7.3 179
  53.0103 1.4 34
  53.0168 0.9 22
  53.0468 4.4 108
  54.0399 0.5 12
  55.0302 0.4 9
  62.0249 1.1 27
  63.029 2.6 63
  64.037 0.5 12
  65.0457 7.9 193
  66.0429 5.9 144
  67.0463 1.3 31
  67.0529 0.6 14
  67.062 0.9 22
  68.0183 0.4 9
  68.0573 0.4 9
  68.985 1.8 44
  69.9928 0.9 22
  71.996 0.6 14
  76.0231 0.8 19
  77.0437 11.9 292
  78.0381 9.7 238
  79.025 1 24
  79.0475 26.6 652
  80.0172 2.8 68
  80.0361 0.7 17
  80.0538 9 220
  81.9907 0.5 12
  83.0005 2.2 54
  84.0016 0.5 12
  85.015 0.5 12
  89.0423 1.7 41
  90.0372 1.3 31
  91.0448 2.4 58
  92.0529 6.9 169
  93.0487 9.9 242
  94.0677 1.5 36
  94.998 1.3 31
  96.0073 1.5 36
  97.0141 4.7 115
  102.0368 0.5 12
  104.0519 2.1 51
  105.0473 5.3 130
  106.0331 0.5 12
  106.0638 40.7 999
  107.0754 3.6 88
  108.0496 0.7 17
  108.0828 1.3 31
  109.0106 0.8 19
  110.009 4.1 100
  117.0486 0.4 9
  118.0306 0.6 14
  118.0529 0.4 9
  119.0588 0.6 14
  120.0485 0.7 17
  122.0083 1.6 39
  123.0165 1.1 27
  124.0235 0.9 22
  133.0419 1.1 27
  134.0102 1.5 36
  134.0484 5.1 125
  136.0243 1.2 29
  137.0172 12.4 304
  138.029 0.6 14
  140.0532 0.6 14
  151.0112 0.7 17
  152.0177 1.4 34
  153.0412 0.5 12
  155.0633 0.5 12
  165.0125 1.3 31
  166.035 0.5 12
  166.0615 0.4 9
  167.0595 1 24
  168.0685 0.6 14
  179.0627 0.6 14
  194.0729 0.9 22
  222.0687 0.4 9
//

system version 2.2.6-SNAPSHOT
Copyright © 2006 MassBank Project; 2011 NORMAN Association; 2021 MassBank Consortium
de.NBI logo
EAWAG logo
fnr logo
IPB logo
NORMAN logo
UFZ logo
LCSB logo
HBM4EU logo
nfdi4chem logo