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-Athens_Univ-AU281602

17alpha-Methyltestosterone; LC-ESI-QTOF; MS2; CE: 20 eV; R=35000; [M+H]+

Mass Spectrum
150.0200.0250.0300.0m/z0.000200.0400.0600.0800.01000Abundance
Chemical Structure
Generated by the Chemistry Development Kit (http://github.com/cdk)

ACCESSION: MSBNK-Athens_Univ-AU281602
RECORD_TITLE: 17alpha-Methyltestosterone; LC-ESI-QTOF; MS2; CE: 20 eV; R=35000; [M+H]+
DATE: 2019.05.31
AUTHORS: Nikiforos Alygizakis, Katerina Galani, Nikolaos Thomaidis, University of Athens
LICENSE: CC BY
COPYRIGHT: Copyright (C) 2019 Department of Chemistry, University of Athens
COMMENT: CONFIDENCE standard compound
COMMENT: INTERNAL_ID 2816

CH$NAME: 17alpha-Methyltestosterone
CH$NAME: Methyltestosterone
CH$NAME: (8R,9S,10R,13S,14S,17S)-17-hydroxy-10,13,17-trimethyl-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-3-one
CH$COMPOUND_CLASS: N/A; Environmental Standard
CH$FORMULA: C20H30O2
CH$EXACT_MASS: 302.2245802
CH$SMILES: C[C@]1(O)CC[C@H]2[C@@H]3CCC4=CC(=O)CC[C@]4(C)[C@H]3CC[C@]12C
CH$IUPAC: InChI=1S/C20H30O2/c1-18-9-6-14(21)12-13(18)4-5-15-16(18)7-10-19(2)17(15)8-11-20(19,3)22/h12,15-17,22H,4-11H2,1-3H3/t15-,16+,17+,18+,19+,20+/m1/s1
CH$LINK: CAS 58-18-4
CH$LINK: CHEBI 27436
CH$LINK: KEGG C07198
CH$LINK: LIPIDMAPS LMST02020029
CH$LINK: PUBCHEM CID:6010
CH$LINK: INCHIKEY GCKMFJBGXUYNAG-HLXURNFRSA-N
CH$LINK: CHEMSPIDER 5788
CH$LINK: COMPTOX DTXSID1033664

AC$INSTRUMENT: Bruker maXis Impact
AC$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: FRAGMENTATION_MODE CID
AC$MASS_SPECTROMETRY: COLLISION_ENERGY 20 eV
AC$MASS_SPECTROMETRY: RESOLUTION 35000
AC$CHROMATOGRAPHY: COLUMN_NAME Acclaim RSLC C18 2.2um, 2.1x100mm, Thermo
AC$CHROMATOGRAPHY: FLOW_GRADIENT 99/1 at 0-1 min, 61/39 at 3 min, 0.1/99.9 at 14-16 min, 99/1 at 16.1-20 min
AC$CHROMATOGRAPHY: FLOW_RATE 200 uL/min at 0-3 min, 400 uL/min at 14 min, 480 uL/min at 16-19 min, 200 uL/min at 19.1-20 min
AC$CHROMATOGRAPHY: RETENTION_TIME 10.354 min
AC$CHROMATOGRAPHY: SOLVENT A 90:10 water:methanol with 0.01% formic acid and 5mM ammonium formate
AC$CHROMATOGRAPHY: SOLVENT B methanol with 0.01% formic acid and 5mM ammonium formate

MS$FOCUSED_ION: BASE_PEAK 303.2322
MS$FOCUSED_ION: PRECURSOR_M/Z 303.2319
MS$FOCUSED_ION: PRECURSOR_TYPE [M+H]+
MS$DATA_PROCESSING: RECALIBRATE identity on assigned fragments and MS1
MS$DATA_PROCESSING: WHOLE RMassBank 2.10.1

PK$SPLASH: splash10-0udi-0239000000-43f151b93c4dd48b4ff5
PK$ANNOTATION: m/z tentative_formula formula_count mass error(ppm)
  121.1006 C9H13+ 1 121.1012 -4.36
  123.0795 C8H11O+ 1 123.0804 -7.98
  133.1006 C10H13+ 1 133.1012 -4.57
  135.116 C10H15+ 1 135.1168 -6.42
  145.1003 C11H13+ 1 145.1012 -5.96
  147.1163 C11H15+ 1 147.1168 -3.86
  149.1315 C11H17+ 1 149.1325 -6.73
  159.116 C12H15+ 1 159.1168 -5.44
  161.1318 C12H17+ 1 161.1325 -4.44
  163.1107 C11H15O+ 1 163.1117 -6.21
  163.1469 C12H19+ 1 163.1481 -7.6
  171.1157 C13H15+ 1 171.1168 -6.34
  173.1316 C13H17+ 1 173.1325 -5.12
  175.1472 C13H19+ 1 175.1481 -5.07
  177.1264 C12H17O+ 1 177.1274 -5.32
  177.1631 C13H21+ 1 177.1638 -3.65
  185.1317 C14H17+ 1 185.1325 -4.3
  187.1476 C14H19+ 1 187.1481 -3.01
  189.1633 C14H21+ 1 189.1638 -2.29
  190.1659 C13[13]CH21+ 1 190.1677 -9.13
  199.1475 C15H19+ 1 199.1481 -3.32
  201.1633 C15H21+ 1 201.1638 -2.54
  203.1789 C15H23+ 1 203.1794 -2.72
  211.1472 C16H19+ 1 211.1481 -4.42
  215.1793 C16H23+ 1 215.1794 -0.4
  225.1636 C17H21+ 1 225.1638 -0.87
  227.1793 C17H23+ 1 227.1794 -0.36
  228.182 C16[13]CH23+ 1 228.1833 -5.99
  229.1583 C16H21O+ 1 229.1587 -1.82
  243.1742 C17H23O+ 1 243.1743 -0.6
  245.1897 C17H25O+ 1 245.19 -1.15
  246.193 C16[13]CH25O+ 1 246.1939 -3.72
  267.2111 C20H27+ 1 267.2107 1.25
  268.2143 C19[13]CH27+ 1 268.2146 -1.33
  285.2217 C20H29O+ 1 285.2213 1.43
  286.2247 C19[13]CH29O+ 1 286.2252 -1.72
  303.2326 C20H31O2+ 1 303.2319 2.58
  304.2359 C19[13]CH31O2+ 1 304.2358 0.61
  305.2387 C18[13]C2H31O2+ 1 305.2391 -1.23
PK$NUM_PEAK: 39
PK$PEAK: m/z int. rel.int.
  121.1006 9140 8
  123.0795 11340 10
  133.1006 10016 9
  135.116 10392 9
  145.1003 8084 7
  147.1163 6924 6
  149.1315 8732 7
  159.116 18948 17
  161.1318 12964 11
  163.1107 7184 6
  163.1469 6416 5
  171.1157 8372 7
  173.1316 9324 8
  175.1472 14488 13
  177.1264 19972 18
  177.1631 30772 27
  185.1317 9760 8
  187.1476 8616 7
  189.1633 69268 62
  190.1659 11024 10
  199.1475 6408 5
  201.1633 15044 13
  203.1789 19120 17
  211.1472 17084 15
  215.1793 10212 9
  225.1636 8412 7
  227.1793 44256 40
  228.182 7932 7
  229.1583 13588 12
  243.1742 5868 5
  245.1897 45536 41
  246.193 8472 7
  267.2111 85152 77
  268.2143 20152 18
  285.2217 231112 210
  286.2247 45328 41
  303.2326 1099272 999
  304.2359 204156 185
  305.2387 20856 18
//

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