ACCESSION: MSBNK-LCSB-LU134306
RECORD_TITLE: Cladribine; LC-ESI-QFT; MS2; CE: 90; 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 1343
COMMENT: DATASET 20200303_ENTACT_RP_MIX504
COMMENT: DATA_PROCESSING MERGING RMBmix ver. 0.2.7
COMMENT: DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0
COMMENT: ORIGINAL_ACQUISITION_NO 5653
COMMENT: ORIGINAL_PRECURSOR_SCAN_NO 5650
COMMENT: RAW_DATA available as MSV000091754 at [DOI:10.25345/C5S46HG75]

CH$NAME: Cladribine
CH$COMPOUND_CLASS: N/A; Environmental Standard
CH$FORMULA: C₁₀H₁₂ClN₅O₃
CH$EXACT_MASS: 285.0629
CH$SMILES: NC1=NC(Cl)=NC2=C1N=CN2[C@H]1C[C@H](O)[C@@H](CO)O1
CH$IUPAC: InChI=1S/C10H12ClN5O3/c11-10-14-8(12)7-9(15-10)16(3-13-7)6-1-4(18)5(2-17)19-6/h3-6,17-18H,1-2H2,(H2,12,14,15)/t4-,5+,6+/m0/s1
CH$LINK: CAS 4291-63-8
CH$LINK: CHEBI 567361
CH$LINK: KEGG D01370
CH$LINK: PUBCHEM CID:20279
CH$LINK: INCHIKEY PTOAARAWEBMLNO-KVQBGUIXSA-N
CH$LINK: CHEMSPIDER 19105

AC$INSTRUMENT: Q Exactive Orbitrap (Thermo Scientific)
AC$INSTRUMENT_TYPE: LC-ESI-QFT
AC$MASS_SPECTROMETRY: MS_TYPE MS2
AC$MASS_SPECTROMETRY: ION_MODE POSITIVE
AC$MASS_SPECTROMETRY: IONIZATION ESI
AC$MASS_SPECTROMETRY: FRAGMENTATION_MODE HCD
AC$MASS_SPECTROMETRY: COLLISION_ENERGY 90
AC$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 10.837 min
AC$CHROMATOGRAPHY: SOLVENT A 0.1% formic acid
AC$CHROMATOGRAPHY: SOLVENT B methanol

MS$FOCUSED_ION: BASE_PEAK 79.0212
MS$FOCUSED_ION: PRECURSOR_M/Z 286.0701
MS$FOCUSED_ION: PRECURSOR_TYPE [M+H]+
MS$FOCUSED_ION: PRECURSOR_INTENSITY 2515544
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$SPLASH: splash10-001i-2900000000-0f8325b5c155b999e5e0
PK$ANNOTATION: m/z tentative_formula formula_count mass error(ppm)
  53.0022 C3HO+ 2 53.0022 -0.3
  53.0386 C4H5+ 1 53.0386 0.98
  55.018 C3H3O+ 2 55.0178 2.2
  57.0335 C3H5O+ 2 57.0335 -0.4
  69.0335 C4H5O+ 2 69.0335 0.16
  70.04 C2H4N3+ 1 70.04 -0.33
  71.0491 C4H7O+ 2 71.0491 -0.21
  73.0284 C3H5O2+ 2 73.0284 -0.04
  80.0243 C3H2N3+ 1 80.0243 -0.1
  81.0335 C5H5O+ 2 81.0335 -0.23
  92.0243 C4H2N3+ 3 92.0243 0.28
  99.0442 C5H7O2+ 4 99.0441 1.17
  107.0352 C4H3N4+ 3 107.0352 0.23
  117.0546 C5H9O3+ 4 117.0546 0.12
  134.0462 C5H4N5+ 4 134.0461 0.3
  135.0301 C5H3N4O+ 4 135.0301 -0.09
  152.0568 C5H6N5O+ 3 152.0567 0.56
  170.0229 C5H5ClN5+ 4 170.0228 0.34
  171.0069 C5H4ClN4O+ 4 171.0068 0.21
PK$NUM_PEAK: 19
PK$PEAK: m/z int. rel.int.
  53.0022 7740.9 15
  53.0386 16036.2 31
  55.018 1997.7 3
  57.0335 6207.6 12
  69.0335 31585.3 61
  70.04 2007.2 3
  71.0491 15317.3 29
  73.0284 37305.4 72
  80.0243 28717.7 56
  81.0335 8312 16
  92.0243 23026.4 44
  99.0442 3849.1 7
  107.0352 148174 289
  117.0546 1863.8 3
  134.0462 512167.6 999
  135.0301 12485 24
  152.0568 49812 97
  170.0229 66417.9 129
  171.0069 4624.5 9
//