ACCESSION: MSBNK-LCSB-LU108552
RECORD_TITLE: Amiloride; LC-ESI-QFT; MS2; CE: 30; R=17500; [M-H]-
DATE: 2020.08.19
AUTHORS: Elapavalore, A.; Kondić, T.; Singh, R.; Schymanski, E.
LICENSE: CC BY
COPYRIGHT: Copyright © 2019 by Environmental Cheminformatics, LCSB, University of Luxembourg, Luxembourg
PUBLICATION: Elapavalore, A.; Kondić, T.; et al., Adding Open Spectral Data to MassBank and PubChem Using Open Source Tools to Support Non-Targeted Exposomics of Mixtures (submitted).
PROJECT: ENTACT U.S. Environmental Protection Agency’s Non-Targeted Analysis Collaborative Trial
COMMENT: CONFIDENCE standard compound
COMMENT: INTERNAL_ID 1085
COMMENT: DATASET 20200303_ENTACT_RP_MIX505
COMMENT: DATA_PROCESSING MERGING RMBmix ver. 0.2.7
COMMENT: DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0
COMMENT: ORIGINAL_ACQUISITION_NO 2373
COMMENT: ORIGINAL_PRECURSOR_SCAN_NO 2370
COMMENT: RAW_DATA available as MSV000091754 at [DOI:10.25345/C5S46HG75]

CH$NAME: Amiloride
CH$NAME: 3,5-diamino-6-chloro-N-(diaminomethylidene)pyrazine-2-carboxamide
CH$COMPOUND_CLASS: N/A; Environmental Standard
CH$FORMULA: C₆H₈ClN₇O
CH$EXACT_MASS: 229.0479
CH$SMILES: NC(=N)NC(=O)C1=NC(Cl)=C(N)N=C1N
CH$IUPAC: InChI=1S/C6H8ClN7O/c7-2-4(9)13-3(8)1(12-2)5(15)14-6(10)11/h(H4,8,9,13)(H4,10,11,14,15)
CH$LINK: CAS 2016-88-8
CH$LINK: CHEBI 2639
CH$LINK: KEGG D07447
CH$LINK: PUBCHEM CID:16231
CH$LINK: INCHIKEY XSDQTOBWRPYKKA-UHFFFAOYSA-N
CH$LINK: CHEMSPIDER 15403

AC$INSTRUMENT: Q Exactive Orbitrap (Thermo Scientific)
AC$INSTRUMENT_TYPE: LC-ESI-QFT
AC$MASS_SPECTROMETRY: MS_TYPE MS2
AC$MASS_SPECTROMETRY: ION_MODE NEGATIVE
AC$MASS_SPECTROMETRY: IONIZATION ESI
AC$MASS_SPECTROMETRY: FRAGMENTATION_MODE HCD
AC$MASS_SPECTROMETRY: COLLISION_ENERGY 30
AC$MASS_SPECTROMETRY: RESOLUTION 17500
AC$CHROMATOGRAPHY: COLUMN_NAME Acquity BEH C18 1.7um, 2.1x150mm (Waters)
AC$CHROMATOGRAPHY: FLOW_GRADIENT 90/10 at 0-2 min, 0/100 at 15-20 min, 90/10 at 20.1-30 min
AC$CHROMATOGRAPHY: FLOW_RATE 0.20 mL/min
AC$CHROMATOGRAPHY: RETENTION_TIME 9.296 min
AC$CHROMATOGRAPHY: SOLVENT A 0.1% formic acid
AC$CHROMATOGRAPHY: SOLVENT B methanol

MS$FOCUSED_ION: BASE_PEAK 228.0407
MS$FOCUSED_ION: PRECURSOR_M/Z 228.0406
MS$FOCUSED_ION: PRECURSOR_TYPE [M-H]-
MS$FOCUSED_ION: PRECURSOR_INTENSITY 2523473.341553
MS$DATA_PROCESSING: RECALIBRATE loess on assigned fragments and MS1
MS$DATA_PROCESSING: REANALYZE Peaks with additional N2/O included
MS$DATA_PROCESSING: WHOLE RMassBank 2.99.2

PK$SPLASH: splash10-000f-0900000000-b9b34ab84226fae59701
PK$ANNOTATION: m/z tentative_formula formula_count mass error(ppm)
  65.0145 C3HN2- 1 65.0145 -0.36
  66.0098 C2N3- 1 66.0098 0.5
  84.0203 C2H2N3O- 1 84.0203 -0.61
  90.0097 C4N3- 1 90.0098 -0.97
  106.0049 C4N3O- 2 106.0047 1.82
  107.0363 C4H3N4- 2 107.0363 0.13
  108.0204 C4H2N3O- 3 108.0203 0.27
  133.0158 C5HN4O- 3 133.0156 1.43
  143.013 C4H4ClN4- 2 143.013 0.03
  150.0421 C5H4N5O- 2 150.0421 -0.22
  168.0081 C5H3ClN5- 1 168.0082 -0.67
  168.9922 C5H2ClN4O- 2 168.9923 -0.07
  186.0188 C5H5ClN5O- 2 186.0188 0.15
  187.0024 C3H2ClN7O- 1 187.0015 4.93
  211.0141 C6H4ClN6O- 1 211.0141 0.17
  228.0407 C6H7ClN7O- 1 228.0406 0.2
PK$NUM_PEAK: 16
PK$PEAK: m/z int. rel.int.
  65.0145 40353.8 54
  66.0098 7907.1 10
  84.0203 1996.9 2
  90.0097 4638.1 6
  106.0049 2443.1 3
  107.0363 26178.6 35
  108.0204 142802 193
  133.0158 1846.3 2
  143.013 736102 999
  150.0421 36577.7 49
  168.0081 15641.2 21
  168.9922 86207.7 116
  186.0188 559504.9 759
  187.0024 2733.8 3
  211.0141 43904.2 59
  228.0407 116777.4 158
//