This website uses technical necessary cookies (e.g. session ID) and in addition the Matomo web analytics tool. Matomo enables us to evaluate the use of our website in compliance with GDPR (Directive 95/46/EC). Data Privacy Policy
This banner can be opend with the 'Data Privacy'-button. Your consent to the use of Matomo can be revoked any time. To make that choice, please un-check below.

MassBank MassBank Search Contents Download

MassBank Record: MSBNK-Eawag-EQ313604

Fluvastatin; LC-ESI-QFT; MS2; CE: 60; R=35000; [M+H]+

Mass Spectrum
100.0150.0200.0250.0300.0m/z0.000200.0400.0600.0800.01000Abundance
Chemical Structure
Generated by the Chemistry Development Kit (http://github.com/cdk)

ACCESSION: MSBNK-Eawag-EQ313604
RECORD_TITLE: Fluvastatin; LC-ESI-QFT; MS2; CE: 60; R=35000; [M+H]+
DATE: 2015.08.25
AUTHORS: Beck B, Stravs M, Schymanski E, Singer H, Department of Environmental Chemistry, Eawag
LICENSE: CC BY
COPYRIGHT: Copyright (C) 2015 Eawag, Duebendorf, Switzerland
COMMENT: CONFIDENCE standard compound
COMMENT: EAWAG_UCHEM_ID 3136

CH$NAME: Fluvastatin
CH$NAME: (3R,5S)-7-[3-(4-fluorophenyl)-1-isopropyl-2-indolyl]-3,5-dihydroxy-6-heptenoic acid
CH$COMPOUND_CLASS: N/A; Environmental Standard
CH$FORMULA: C24H26FNO4
CH$EXACT_MASS: 411.18459
CH$SMILES: O=C(O)C[C@H](O)C[C@H](O)/C=C/c2c(c1ccccc1n2C(C)C)c3ccc(F)cc3
CH$IUPAC: InChI=1S/C24H26FNO4/c1-15(2)26-21-6-4-3-5-20(21)24(16-7-9-17(25)10-8-16)22(26)12-11-18(27)13-19(28)14-23(29)30/h3-12,15,18-19,27-28H,13-14H2,1-2H3,(H,29,30)/b12-11+/t18-,19-/m1/s1
CH$LINK: CAS 93957-54-1
CH$LINK: PUBCHEM CID:146801
CH$LINK: INCHIKEY FJLGEFLZQAZZCD-MCBHFWOFSA-N
CH$LINK: CHEMSPIDER 393587
CH$LINK: COMPTOX DTXSID2020636

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$MASS_SPECTROMETRY: COLLISION_ENERGY 60 (nominal)
AC$MASS_SPECTROMETRY: RESOLUTION 35000
AC$CHROMATOGRAPHY: COLUMN_NAME XBridge C18 3.5um, 2.1x50mm, Waters
AC$CHROMATOGRAPHY: FLOW_GRADIENT 90/10 at 0 min, 50/50 at 4 min, 5/95 at 17 min, 5/95 at 25 min, 90/10 at 25.1 min, 90/10 at 30 min
AC$CHROMATOGRAPHY: FLOW_RATE 200 ul/min
AC$CHROMATOGRAPHY: RETENTION_TIME 13.5 min
AC$CHROMATOGRAPHY: SOLVENT A water with 0.1% formic acid
AC$CHROMATOGRAPHY: SOLVENT B methanol with 0.1% formic acid

MS$FOCUSED_ION: BASE_PEAK 412.1916
MS$FOCUSED_ION: PRECURSOR_M/Z 412.1919
MS$FOCUSED_ION: PRECURSOR_TYPE [M+H]+
MS$DATA_PROCESSING: DEPROFILE Spline
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 1.9.6

PK$SPLASH: splash10-00di-0290000000-4a295990449f9a691802
PK$ANNOTATION: m/z tentative_formula formula_count mass error(ppm)
  67.0542 C5H7+ 1 67.0542 -0.4
  69.0335 C4H5O+ 1 69.0335 -0.6
  71.0126 C3H3O2+ 1 71.0128 -1.49
  71.0491 C4H7O+ 1 71.0491 -1
  81.0334 C5H5O+ 1 81.0335 -1
  89.0233 C3H5O3+ 1 89.0233 -0.68
  95.049 C6H7O+ 1 95.0491 -0.96
  97.0284 C5H5O2+ 1 97.0284 -0.16
  122.0398 C7H5FN+ 1 122.0401 -2
  123.0439 C7H7O2+ 1 123.0441 -1.19
  141.0546 C7H9O3+ 1 141.0546 -0.29
  143.0854 C11H11+ 1 143.0855 -0.61
  168.0806 C12H10N+ 1 168.0808 -1.28
  177.0697 C14H9+ 1 177.0699 -0.94
  196.0682 C14H9F+ 1 196.0683 -0.46
  197.076 C14H10F+ 1 197.0761 -0.43
  204.0808 C15H10N+ 1 204.0808 0.07
  209.0634 C14H8FN+ 1 209.0635 -0.47
  211.0793 C14H10FN+ 1 211.0792 0.62
  212.087 C14H11FN+ 1 212.087 -0.25
  218.0965 C16H12N+ 1 218.0964 0.16
  222.0714 C15H9FN+ 1 222.0714 0.03
  223.0793 C15H10FN+ 1 223.0792 0.36
  224.0869 C15H11FN+ 1 224.087 -0.55
  225.0908 C15H13O2+ 1 225.091 -0.92
  235.0793 C16H10FN+ 1 235.0792 0.39
  236.0871 C16H11FN+ 1 236.087 0.24
  237.0943 C16H12FN+ 1 237.0948 -2.06
  238.1025 C16H13FN+ 1 238.1027 -0.48
  248.087 C17H11FN+ 1 248.087 -0.06
  249.095 C17H12FN+ 1 249.0948 0.69
  250.103 C17H13FN+ 1 250.1027 1.54
  251.111 C17H14FN+ 1 251.1105 1.92
  253.126 C17H16FN+ 1 253.1261 -0.63
  261.0947 C18H12FN+ 1 261.0948 -0.3
  262.1029 C18H13FN+ 1 262.1027 0.79
  264.1181 C18H15FN+ 1 264.1183 -0.77
  266.134 C18H17FN+ 1 266.134 0.13
  274.1023 C19H13FN+ 1 274.1027 -1.26
  288.118 C20H15FN+ 1 288.1183 -1.06
PK$NUM_PEAK: 40
PK$PEAK: m/z int. rel.int.
  67.0542 1891897 8
  69.0335 800568.9 3
  71.0126 1261261.8 5
  71.0491 781368.5 3
  81.0334 1370457.6 6
  89.0233 353698.8 1
  95.049 6536424.1 30
  97.0284 1549389.6 7
  122.0398 905940.7 4
  123.0439 4613062.3 21
  141.0546 213257.9 1
  143.0854 235140.5 1
  168.0806 533321.3 2
  177.0697 4371688.8 20
  196.0682 11350693.4 53
  197.076 55673491.2 262
  204.0808 10949140.3 51
  209.0634 678935.8 3
  211.0793 2398338.2 11
  212.087 3947912.6 18
  218.0965 388402.3 1
  222.0714 9935735.7 46
  223.0793 29971459.3 141
  224.0869 211534009.3 999
  225.0908 365791 1
  235.0793 1189542.6 5
  236.0871 1491986 7
  237.0943 585099.8 2
  238.1025 10494019.6 49
  248.087 2369966.7 11
  249.095 1137001.7 5
  250.103 889647.4 4
  251.111 663888.9 3
  253.126 449543 2
  261.0947 489110.7 2
  262.1029 877563.6 4
  264.1181 1893817.1 8
  266.134 6110730.7 28
  274.1023 1808022.3 8
  288.118 1036554.1 4
//

Imprint Feedback
system version 2.2.8

Copyright © 2006 MassBank Project; 2011 NORMAN Association; 2021 MassBank Consortium

Responsible: Tillmann G. Fischer

Funded by the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) under the National Research Data Infrastructure – NFDI4Chem – Projektnummer 441958208.

de.NBI logo
EAWAG logo
fnr logo
IPB logo
NORMAN logo
UFZ logo
LCSB logo
HBM4EU logo
nfdi4chem logo