MassBank Record: AC000252

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Trichoverrol A; LC-ESI-ITFT; MS2; CE: 50; R=17500; [M+H]+

Mass Spectrum
Chemical Structure
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ACCESSION: AC000252
RECORD_TITLE: Trichoverrol A; LC-ESI-ITFT; MS2; CE: 50; R=17500; [M+H]+
DATE: 2017.07.07
AUTHORS: Justin B. Renaud, J. David Miller, Mark W. Sumarah, Agriculture and Agri-Food Canada
LICENSE: CC BY-SA
COPYRIGHT: Copyright (C) 2017
PUBLICATION: Renaud, J. B.; Sumarah, M. W. Data Independent Acquisition-Digital Archiving Mass Spectrometry: Application to Single Kernel Mycotoxin Analysis of Fusarium Graminearum Infected Maize. Analytical and Bioanalytical Chemistry 2016, 408 (12), 3083–91. DOI:10.1007/s00216-016-9391-5
COMMENT: CONFIDENCE isolated standard

CH$NAME: Trichoverrol A
CH$NAME: [4b(2Z,4E,6S,7S)]-4-(6,7-dihydroxy-2,4-octadienoate) 12,13-Epoxy-trichothec-9-ene-4,15-diol
CH$COMPOUND_CLASS: Natural Product; Fungal metabolite
CH$FORMULA: C23H32O7
CH$EXACT_MASS: 420.21480000000002519300323911011219024658203125
CH$SMILES: CC1=C[C@@H]2[C@](CC1)([C@]3([C@@H](C[C@H]([C@@]34CO4)O2)OC(=O)/C=C\C=C\[C@@H]([C@H](C)O)O)C)CO
CH$IUPAC: InChI=1S/C23H32O7/c1-14-8-9-22(12-24)18(10-14)29-19-11-17(21(22,3)23(19)13-28-23)30-20(27)7-5-4-6-16(26)15(2)25/h4-7,10,15-19,24-26H,8-9,11-13H2,1-3H3/b6-4+,7-5-/t15-,16-,17+,18+,19+,21+,22+,23-/m0/s1
CH$LINK: CAS 76739-71-4
CH$LINK: CHEMSPIDER 10274911
CH$LINK: INCHIKEY QFKRKMXPKBHGGO-OYWHZMLYSA-N
CH$LINK: KNAPSACK C00012661
CH$LINK: PUBCHEM CID:101649339

AC$INSTRUMENT: Q-Exactive Orbitrap Thermo Scientific
AC$INSTRUMENT_TYPE: LC-ESI-ITFT
AC$MASS_SPECTROMETRY: MS_TYPE MS2
AC$MASS_SPECTROMETRY: ION_MODE POSITIVE
AC$MASS_SPECTROMETRY: COLLISION_ENERGY 50(NCE)
AC$MASS_SPECTROMETRY: FRAGMENTATION_MODE HCD
AC$MASS_SPECTROMETRY: IONIZATION ESI
AC$MASS_SPECTROMETRY: IONIZATION_VOLTAGE 3.9 kV
AC$MASS_SPECTROMETRY: RESOLUTION 17500
AC$CHROMATOGRAPHY: COLUMN_NAME Agilent RRHD Eclipse 50 x 2 mm, 1.8 uM
AC$CHROMATOGRAPHY: FLOW_GRADIENT 100:0 at 0 min, 100:0 at 0.5 min, 0:100 at 3.5 min, 0:100 at 5.5 min, 100:0 at 7 min
AC$CHROMATOGRAPHY: FLOW_RATE 0.3 mL min-1
AC$CHROMATOGRAPHY: NAPS_RTI 1016
AC$CHROMATOGRAPHY: RETENTION_TIME 3.3
AC$CHROMATOGRAPHY: SOLVENT A H2O 0.1% FA
AC$CHROMATOGRAPHY: SOLVENT B ACN 0.1% FA

MS$FOCUSED_ION: BASE_PEAK 81.0703
MS$FOCUSED_ION: PRECURSOR_M/Z 421.2215
MS$FOCUSED_ION: PRECURSOR_TYPE [M+H]+
MS$DATA_PROCESSING: DEPROFILE Proteowizard
MS$DATA_PROCESSING: INTENSITY CUTOFF 0.05 Base Peak
MS$DATA_PROCESSING: RECALIBRATE based on Fragment ion formula determination

PK$SPLASH: splash10-0a59-6900000000-6e8ed68996f05178b356
PK$ANNOTATION: 67.0548 C5H7+ 8.41
  93.0699 C7H9+ 0.13
  107.0855 C8H11+ -0.37
  117.0699 C9H9+ 0.1
  123.0804 C8H11O1+ -0.41
PK$NUM_PEAK: 41
PK$PEAK: m/z int. rel.int.
  55.0549 5525.45751953125 97
  63.128 2391.620849609375 41
  67.0542 4539.4736328125 80
  69.0335 3484.7822265625 61
  79.0542 12769.8310546875 227
  81.0699 55990.55859375 999
  83.0491 18567.80859375 330
  90.977 3993.857666015625 70
  91.0542 6812.28515625 120
  93.0699 24614.33984375 438
  95.0491 11116.9541015625 197
  95.0855 11689.1943359375 207
  105.0699 35596.8671875 634
  106.7353 2435.839111328125 42
  107.0855 37959.73046875 676
  109.0648 14475.556640625 257
  117.0699 3851.992919921875 67
  119.0855 5212.16259765625 92
  121.0648 4982.44970703125 87
  123.0804 21456.662109375 382
  125.0597 4890.888671875 86
  129.0699 4114.32275390625 72
  129.1652 2655.129150390625 46
  131.0855 6120.0546875 108
  133.1012 10578.349609375 187
  139.8399 2762.89111328125 48
  143.0855 16856.7109375 300
  145.1012 9389.9111328125 166
  147.1168 5215.11376953125 92
  155.0855 3969.587890625 69
  156.0934 3734.794677734375 65
  157.1012 4348.12890625 76
  161.0961 17071.3203125 303
  170.109 3541.5634765625 62
  175.1118 4079.73486328125 71
  175.7122 3053.876953125 53
  183.1168 2623.332275390625 45
  201.1274 3639.738037109375 64
  222.3182 3111.795654296875 54
  295.4428 3208.03271484375 56
  353.4109 2858.83251953125 50
//