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Name
Formula / Structure
ExactMass
ID
Kojic acid
12 spectra
C6H6O4
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
142.02660
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003794
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003311
LC-ESI-ITFT; MS2; CE: 20%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003795
LC-ESI-ITFT; MS2; CE: 20%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003313
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003796
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003315
LC-ESI-ITFT; MS2; CE: 40%; R=7500; [M+H]+
MSBNK-HBM4EU-HB004098
LC-ESI-ITFT; MS2; CE: 40%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003312
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M+H]+
MSBNK-HBM4EU-HB004099
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003314
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M+H]+
MSBNK-HBM4EU-HB004100
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003316
Lateropyrone
12 spectra
C15H10O8
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
318.03760
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003837
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003350
LC-ESI-ITFT; MS2; CE: 20%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003838
LC-ESI-ITFT; MS2; CE: 20%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003351
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003839
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003352
LC-ESI-ITFT; MS2; CE: 40%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003840
LC-ESI-ITFT; MS2; CE: 40%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003353
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003841
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003354
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003842
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003355
Lovastatin
6 spectra
C24H36O5
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
404.25629
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003990
LC-ESI-ITFT; MS2; CE: 20%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003991
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003992
LC-ESI-ITFT; MS2; CE: 40%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003993
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003994
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003995
Malformin A1
12 spectra
C23H39N5O5S2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
529.23932
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003972
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003484
LC-ESI-ITFT; MS2; CE: 20%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003973
LC-ESI-ITFT; MS2; CE: 20%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003485
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003974
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003486
LC-ESI-ITFT; MS2; CE: 40%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003975
LC-ESI-ITFT; MS2; CE: 40%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003487
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003976
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003488
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003977
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003489
Malformin C
6 spectra
C23H39N5O5S2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
529.23926
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003490
LC-ESI-ITFT; MS2; CE: 20%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003491
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003492
LC-ESI-ITFT; MS2; CE: 40%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003493
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003494
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003495
Mefruside
107 spectra
C13H19ClN2O5S2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
382.04239
ESI-QTOF; MS2; CE: 10eV; R=15000; [M+H]+
MSBNK-HBM4EU-HB002700
ESI-QTOF; MS2; CE: 15eV; R=15000; [M+H]+
MSBNK-HBM4EU-HB002701
ESI-QTOF; MS2; CE: 20eV; R=15000; [M+H]+
MSBNK-HBM4EU-HB002702
ESI-QTOF; MS2; CE: 25eV; R=15000; [M+H]+
MSBNK-HBM4EU-HB002703
ESI-QTOF; MS2; CE: 30eV; R=15000; [M+H]+
MSBNK-HBM4EU-HB002704
ESI-QTOF; MS2; CE: 35eV; R=15000; [M+H]+
MSBNK-HBM4EU-HB002705
ESI-QTOF; MS2; CE: 40eV; R=15000; [M+H]+
MSBNK-HBM4EU-HB002706
ESI-QTOF; MS2; CE: 45eV; R=15000; [M+H]+
MSBNK-HBM4EU-HB002707
ESI-QTOF; MS2; CE: 50eV; R=15000; [M+H]+
MSBNK-HBM4EU-HB002709
ESI-QTOF; MS2; CE: 5eV; R=15000; [M+H]+
MSBNK-HBM4EU-HB002708
LC-ESI-ITFT; MS2; CE: 10%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001101
LC-ESI-ITFT; MS2; CE: 10%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002364
LC-ESI-ITFT; MS2; CE: 100%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001131
LC-ESI-ITFT; MS2; CE: 100%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001147
LC-ESI-ITFT; MS2; CE: 105%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001136
LC-ESI-ITFT; MS2; CE: 105%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001144
LC-ESI-ITFT; MS2; CE: 110%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001133
LC-ESI-ITFT; MS2; CE: 110%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001149
LC-ESI-ITFT; MS2; CE: 115%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001138
LC-ESI-ITFT; MS2; CE: 115%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001152
LC-ESI-ITFT; MS2; CE: 120%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001135
LC-ESI-ITFT; MS2; CE: 120%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001157
LC-ESI-ITFT; MS2; CE: 125%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001140
LC-ESI-ITFT; MS2; CE: 125%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001154
LC-ESI-ITFT; MS2; CE: 130%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001141
LC-ESI-ITFT; MS2; CE: 130%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001159
LC-ESI-ITFT; MS2; CE: 140%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001143
LC-ESI-ITFT; MS2; CE: 15%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001102
LC-ESI-ITFT; MS2; CE: 15%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001106
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002365
LC-ESI-ITFT; MS2; CE: 150%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001145
LC-ESI-ITFT; MS2; CE: 165%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001156
LC-ESI-ITFT; MS2; CE: 20%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001103
LC-ESI-ITFT; MS2; CE: 20%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001107
LC-ESI-ITFT; MS2; CE: 20%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002366
LC-ESI-ITFT; MS2; CE: 25%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001108
LC-ESI-ITFT; MS2; CE: 25%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002367
LC-ESI-ITFT; MS2; CE: 30%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001105
LC-ESI-ITFT; MS2; CE: 30%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001109
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002368
LC-ESI-ITFT; MS2; CE: 35%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001104
LC-ESI-ITFT; MS2; CE: 35%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001110
LC-ESI-ITFT; MS2; CE: 35%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001112
LC-ESI-ITFT; MS2; CE: 35%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002369
LC-ESI-ITFT; MS2; CE: 40%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001111
LC-ESI-ITFT; MS2; CE: 40%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001117
LC-ESI-ITFT; MS2; CE: 40%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002370
LC-ESI-ITFT; MS2; CE: 45%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001114
LC-ESI-ITFT; MS2; CE: 45%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001116
LC-ESI-ITFT; MS2; CE: 45%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002371
LC-ESI-ITFT; MS2; CE: 5%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002372
LC-ESI-ITFT; MS2; CE: 50%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001113
LC-ESI-ITFT; MS2; CE: 50%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001119
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002373
LC-ESI-ITFT; MS2; CE: 55%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001118
LC-ESI-ITFT; MS2; CE: 55%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001122
LC-ESI-ITFT; MS2; CE: 55%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002374
LC-ESI-ITFT; MS2; CE: 60%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001115
LC-ESI-ITFT; MS2; CE: 60%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001127
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002375
LC-ESI-ITFT; MS2; CE: 65%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001120
LC-ESI-ITFT; MS2; CE: 65%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001124
LC-ESI-ITFT; MS2; CE: 65%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002376
LC-ESI-ITFT; MS2; CE: 70%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001121
LC-ESI-ITFT; MS2; CE: 70%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001129
LC-ESI-ITFT; MS2; CE: 70%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002377
LC-ESI-ITFT; MS2; CE: 75%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001126
LC-ESI-ITFT; MS2; CE: 75%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001132
LC-ESI-ITFT; MS2; CE: 75%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002378
LC-ESI-ITFT; MS2; CE: 80%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001123
LC-ESI-ITFT; MS2; CE: 80%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001137
LC-ESI-ITFT; MS2; CE: 80%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002379
LC-ESI-ITFT; MS2; CE: 85%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001128
LC-ESI-ITFT; MS2; CE: 85%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001134
LC-ESI-ITFT; MS2; CE: 90%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001125
LC-ESI-ITFT; MS2; CE: 90%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001139
LC-ESI-ITFT; MS2; CE: 95%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001130
LC-ESI-ITFT; MS2; CE: 95%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001142
LC-ESI-QFT; MS2; CE: 10%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002141
LC-ESI-QFT; MS2; CE: 10%; R=30000; [M+H]+
MSBNK-HBM4EU-HB001993
LC-ESI-QFT; MS2; CE: 15%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002142
LC-ESI-QFT; MS2; CE: 20%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002143
LC-ESI-QFT; MS2; CE: 20%; R=30000; [M+H]+
MSBNK-HBM4EU-HB001994
LC-ESI-QFT; MS2; CE: 25%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002144
LC-ESI-QFT; MS2; CE: 30%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002145
LC-ESI-QFT; MS2; CE: 35%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002146
LC-ESI-QFT; MS2; CE: 40%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002147
LC-ESI-QFT; MS2; CE: 40%; R=30000; [M+H]+
MSBNK-HBM4EU-HB001995
LC-ESI-QFT; MS2; CE: 45%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002148
LC-ESI-QFT; MS2; CE: 50%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002149
LC-ESI-QFT; MS2; CE: 55%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002150
LC-ESI-QFT; MS2; CE: 60%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002151
LC-ESI-QFT; MS2; CE: 65%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002152
LC-ESI-QFT; MS2; CE: 70%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002153
LC-ESI-QFT; MS2; CE: 75%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002154
LC-ESI-QFT; MS2; CE: 80%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002155
LC-ESI-QFT; MS2; CE: 80%; R=30000; [M+H]+
MSBNK-HBM4EU-HB001996
LC-ESI-QTOF; MS2; CE: 10 eV; R=3600; [M+H]+
MSBNK-HBM4EU-HB002550
LC-ESI-QTOF; MS2; CE: 15 eV; R=3600; [M+H]+
MSBNK-HBM4EU-HB002551
LC-ESI-QTOF; MS2; CE: 20 eV; R=3600; [M+H]+
MSBNK-HBM4EU-HB002552
LC-ESI-QTOF; MS2; CE: 25 eV; R=3600; [M+H]+
MSBNK-HBM4EU-HB002553
LC-ESI-QTOF; MS2; CE: 30 eV; R=3600; [M+H]+
MSBNK-HBM4EU-HB002554
LC-ESI-QTOF; MS2; CE: 35 eV; R=3600; [M+H]+
MSBNK-HBM4EU-HB002555
LC-ESI-QTOF; MS2; CE: 40 eV; R=3600; [M+H]+
MSBNK-HBM4EU-HB002556
LC-ESI-QTOF; MS2; CE: 45 eV; R=3600; [M+H]+
MSBNK-HBM4EU-HB002557
LC-ESI-QTOF; MS2; CE: 5 eV; R=3600; [M+H]+
MSBNK-HBM4EU-HB002559
LC-ESI-QTOF; MS2; CE: 50 eV; R=3600; [M+H]+
MSBNK-HBM4EU-HB002558
Metamitron-desamino (PROBABLE)
1 spectrum
C10H9N3O
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
187.07381
LC-ESI-QFT; MS2; CE: 42%; R=70000; [M+H]+
MSBNK-HBM4EU-HB002880
Metamitron-metabolite (TENTATIVE)
1 spectrum
C9H9N3
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
159.07890
LC-ESI-QFT; MS2; CE: 42%; R=70000; [M+H]+
MSBNK-HBM4EU-HB002881
Metamitron-OH (TENTATIVE)
1 spectrum
C10H10N4O2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
218.07950
LC-ESI-QFT; MS2; CE: 30%; R=70000; [M+H]+
MSBNK-HBM4EU-HB002879
Metazachlor-diOH (TENTATIVE)
2 spectra
C14H16ClN3O3
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
309.08679
LC-ESI-QFT; MS2; CE: 30%; R=70000; [M+H]+
MSBNK-HBM4EU-HB002886
LC-ESI-QFT; MS2; CE: 55%; R=70000; [M+H]+
MSBNK-HBM4EU-HB002887
Metazachlor-N-dealkylation (TENTATIVE)
1 spectrum
C10H12ClNO
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
197.05991
LC-ESI-QFT; MS2; CE: 30%; R=70000; [M+H]+
MSBNK-HBM4EU-HB002882
Metazachlor-OH (TENTATIVE)
3 spectra
C14H16ClN3O2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
293.09180
LC-ESI-QFT; MS2; CE: 30%; R=70000; [M+H]+
MSBNK-HBM4EU-HB002883
LC-ESI-QFT; MS2; CE: 30%; R=70000; [M+H]+
MSBNK-HBM4EU-HB002884
LC-ESI-QFT; MS2; CE: 55%; R=70000; [M+H]+
MSBNK-HBM4EU-HB002885
Metazachlor-OH-deschloro (PROBABLE)
2 spectra
C14H17N3O2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
259.13110
LC-ESI-QFT; MS2; CE: 30%; R=70000; [M+H]+
MSBNK-HBM4EU-HB002888
LC-ESI-QFT; MS2; CE: 55%; R=70000; [M+H]+
MSBNK-HBM4EU-HB002889
Metoclopramide
119 spectra
C14H22ClN3O2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
299.14011
ESI-QTOF; MS2; CE: 10eV; R=15000; [M+H]+
MSBNK-HBM4EU-HB002710
ESI-QTOF; MS2; CE: 15eV; R=15000; [M+H]+
MSBNK-HBM4EU-HB002711
ESI-QTOF; MS2; CE: 20eV; R=15000; [M+H]+
MSBNK-HBM4EU-HB002712
ESI-QTOF; MS2; CE: 25eV; R=15000; [M+H]+
MSBNK-HBM4EU-HB002713
ESI-QTOF; MS2; CE: 30eV; R=15000; [M+H]+
MSBNK-HBM4EU-HB002714
ESI-QTOF; MS2; CE: 35eV; R=15000; [M+H]+
MSBNK-HBM4EU-HB002715
ESI-QTOF; MS2; CE: 40eV; R=15000; [M+H]+
MSBNK-HBM4EU-HB002716
ESI-QTOF; MS2; CE: 45eV; R=15000; [M+H]+
MSBNK-HBM4EU-HB002717
ESI-QTOF; MS2; CE: 50eV; R=15000; [M+H]+
MSBNK-HBM4EU-HB002719
ESI-QTOF; MS2; CE: 5eV; R=15000; [M+H]+
MSBNK-HBM4EU-HB002718
LC-ESI-ITFT; MS2; CE: 10%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001201
LC-ESI-ITFT; MS2; CE: 100%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001231
LC-ESI-ITFT; MS2; CE: 100%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001247
LC-ESI-ITFT; MS2; CE: 105%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001236
LC-ESI-ITFT; MS2; CE: 105%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001244
LC-ESI-ITFT; MS2; CE: 110%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001233
LC-ESI-ITFT; MS2; CE: 110%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001249
LC-ESI-ITFT; MS2; CE: 115%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001238
LC-ESI-ITFT; MS2; CE: 115%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001252
LC-ESI-ITFT; MS2; CE: 120%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001235
LC-ESI-ITFT; MS2; CE: 120%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001257
LC-ESI-ITFT; MS2; CE: 125%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001240
LC-ESI-ITFT; MS2; CE: 125%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001254
LC-ESI-ITFT; MS2; CE: 130%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001241
LC-ESI-ITFT; MS2; CE: 130%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001259
LC-ESI-ITFT; MS2; CE: 135%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001246
LC-ESI-ITFT; MS2; CE: 140%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001243
LC-ESI-ITFT; MS2; CE: 145%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001248
LC-ESI-ITFT; MS2; CE: 15%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001202
LC-ESI-ITFT; MS2; CE: 15%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001206
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002380
LC-ESI-ITFT; MS2; CE: 150%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001245
LC-ESI-ITFT; MS2; CE: 155%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001250
LC-ESI-ITFT; MS2; CE: 160%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001251
LC-ESI-ITFT; MS2; CE: 165%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001256
LC-ESI-ITFT; MS2; CE: 170%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001253
LC-ESI-ITFT; MS2; CE: 175%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001258
LC-ESI-ITFT; MS2; CE: 180%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001255
LC-ESI-ITFT; MS2; CE: 185%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001260
LC-ESI-ITFT; MS2; CE: 20%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001203
LC-ESI-ITFT; MS2; CE: 20%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001207
LC-ESI-ITFT; MS2; CE: 20%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002381
LC-ESI-ITFT; MS2; CE: 25%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001208
LC-ESI-ITFT; MS2; CE: 25%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002382
LC-ESI-ITFT; MS2; CE: 30%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001205
LC-ESI-ITFT; MS2; CE: 30%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001209
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002383
LC-ESI-ITFT; MS2; CE: 35%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001204
LC-ESI-ITFT; MS2; CE: 35%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001210
LC-ESI-ITFT; MS2; CE: 35%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001212
LC-ESI-ITFT; MS2; CE: 35%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002384
LC-ESI-ITFT; MS2; CE: 40%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001211
LC-ESI-ITFT; MS2; CE: 40%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001217
LC-ESI-ITFT; MS2; CE: 40%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002385
LC-ESI-ITFT; MS2; CE: 45%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001214
LC-ESI-ITFT; MS2; CE: 45%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001216
LC-ESI-ITFT; MS2; CE: 45%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002386
LC-ESI-ITFT; MS2; CE: 50%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001213
LC-ESI-ITFT; MS2; CE: 50%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001219
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002387
LC-ESI-ITFT; MS2; CE: 55%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001218
LC-ESI-ITFT; MS2; CE: 55%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001222
LC-ESI-ITFT; MS2; CE: 55%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002388
LC-ESI-ITFT; MS2; CE: 60%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001215
LC-ESI-ITFT; MS2; CE: 60%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001227
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002389
LC-ESI-ITFT; MS2; CE: 65%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001220
LC-ESI-ITFT; MS2; CE: 65%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001224
LC-ESI-ITFT; MS2; CE: 65%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002390
LC-ESI-ITFT; MS2; CE: 70%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001221
LC-ESI-ITFT; MS2; CE: 70%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001229
LC-ESI-ITFT; MS2; CE: 70%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002391
LC-ESI-ITFT; MS2; CE: 75%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001226
LC-ESI-ITFT; MS2; CE: 75%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001232
LC-ESI-ITFT; MS2; CE: 75%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002392
LC-ESI-ITFT; MS2; CE: 80%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001223
LC-ESI-ITFT; MS2; CE: 80%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001237
LC-ESI-ITFT; MS2; CE: 80%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002393
LC-ESI-ITFT; MS2; CE: 85%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001228
LC-ESI-ITFT; MS2; CE: 85%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001234
LC-ESI-ITFT; MS2; CE: 90%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001225
LC-ESI-ITFT; MS2; CE: 90%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001239
LC-ESI-ITFT; MS2; CE: 95%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001230
LC-ESI-ITFT; MS2; CE: 95%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001242
LC-ESI-QFT; MS2; CE: 10%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002156
LC-ESI-QFT; MS2; CE: 10%; R=30000; [M+H]+
MSBNK-HBM4EU-HB001997
LC-ESI-QFT; MS2; CE: 15%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002157
LC-ESI-QFT; MS2; CE: 20%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002158
LC-ESI-QFT; MS2; CE: 20%; R=30000; [M+H]+
MSBNK-HBM4EU-HB001998
LC-ESI-QFT; MS2; CE: 25%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002159
LC-ESI-QFT; MS2; CE: 30%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002160
LC-ESI-QFT; MS2; CE: 35%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002161
LC-ESI-QFT; MS2; CE: 40%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002162
LC-ESI-QFT; MS2; CE: 40%; R=30000; [M+H]+
MSBNK-HBM4EU-HB001999
LC-ESI-QFT; MS2; CE: 45%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002163
LC-ESI-QFT; MS2; CE: 50%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002164
LC-ESI-QFT; MS2; CE: 55%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002165
LC-ESI-QFT; MS2; CE: 60%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002166
LC-ESI-QFT; MS2; CE: 65%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002167
LC-ESI-QFT; MS2; CE: 70%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002168
LC-ESI-QFT; MS2; CE: 75%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002169
LC-ESI-QFT; MS2; CE: 80%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002170
LC-ESI-QFT; MS2; CE: 80%; R=30000; [M+H]+
MSBNK-HBM4EU-HB002000
LC-ESI-QFT; MS2; CE: CE15; R=17500; [M+H]+
MSBNK-HBM4EU-HB002809
LC-ESI-QFT; MS2; CE: CE30; R=17500; [M+H]+
MSBNK-HBM4EU-HB002810
LC-ESI-QFT; MS2; CE: CE45; R=17500; [M+H]+
MSBNK-HBM4EU-HB002811
LC-ESI-QFT; MS2; CE: CE60; R=17500; [M+H]+
MSBNK-HBM4EU-HB002812
LC-ESI-QFT; MS2; CE: CE75; R=17500; [M+H]+
MSBNK-HBM4EU-HB002813
LC-ESI-QFT; MS2; CE: CE90; R=17500; [M+H]+
MSBNK-HBM4EU-HB002814
LC-ESI-QTOF; MS2; CE: 10 eV; R=3600; [M+H]+
MSBNK-HBM4EU-HB002560
LC-ESI-QTOF; MS2; CE: 15 eV; R=3600; [M+H]+
MSBNK-HBM4EU-HB002561
LC-ESI-QTOF; MS2; CE: 20 eV; R=3600; [M+H]+
MSBNK-HBM4EU-HB002562
LC-ESI-QTOF; MS2; CE: 25 eV; R=3600; [M+H]+
MSBNK-HBM4EU-HB002563
LC-ESI-QTOF; MS2; CE: 30 eV; R=3600; [M+H]+
MSBNK-HBM4EU-HB002564
LC-ESI-QTOF; MS2; CE: 35 eV; R=3600; [M+H]+
MSBNK-HBM4EU-HB002565
LC-ESI-QTOF; MS2; CE: 40 eV; R=3600; [M+H]+
MSBNK-HBM4EU-HB002566
LC-ESI-QTOF; MS2; CE: 45 eV; R=3600; [M+H]+
MSBNK-HBM4EU-HB002567
LC-ESI-QTOF; MS2; CE: 5 eV; R=3600; [M+H]+
MSBNK-HBM4EU-HB002569
LC-ESI-QTOF; MS2; CE: 50 eV; R=3600; [M+H]+
MSBNK-HBM4EU-HB002568
Metolachlor-desaturated (TENTATIVE)
1 spectrum
C15H20ClNO2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
281.11710
LC-ESI-QFT; MS2; CE: 42%; R=70000; [M+H]+
MSBNK-HBM4EU-HB002893
Metolachlor-desmethyl (Unequivocal molecular formu...
1 spectrum
C14H16ClNO2
265.08591
LC-ESI-QFT; MS2; CE: 30%; R=70000; [M+H]+
MSBNK-HBM4EU-HB002891
Metolachlor-diOH (TENTATIVE)
2 spectra
C15H22ClNO4
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
315.12280
LC-ESI-QFT; MS2; CE: 30%; R=70000; [M+H]+
MSBNK-HBM4EU-HB002895
LC-ESI-QFT; MS2; CE: 30%; R=70000; [M+H]+
MSBNK-HBM4EU-HB002896
Metolachlor-N-dealkylation (TENTATIVE)
1 spectrum
C11H14ClNO
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
211.07539
LC-ESI-QFT; MS2; CE: 30%; R=70000; [M+H]+
MSBNK-HBM4EU-HB002890
Metolachlor-OH (TENTATIVE)
1 spectrum
C15H22ClNO3
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
299.12881
LC-ESI-QFT; MS2; CE: 30%; R=70000; [M+H]+
MSBNK-HBM4EU-HB002894
Metolachlor-OH-desmethyl (Unequivocal molecular fo...
1 spectrum
C14H20ClNO3
285.11200
LC-ESI-QFT; MS2; CE: 30%; R=70000; [M+H]+
MSBNK-HBM4EU-HB002892
Moniliformin
6 spectra
C4H2O3
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
98.00039
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003069
LC-ESI-ITFT; MS2; CE: 20%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003070
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003071
LC-ESI-ITFT; MS2; CE: 40%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003072
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003073
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003074
Mycophenolic Acid
12 spectra
C17H20O6
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
320.12601
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003704
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003204
LC-ESI-ITFT; MS2; CE: 20%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003705
LC-ESI-ITFT; MS2; CE: 20%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003205
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003706
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003206
LC-ESI-ITFT; MS2; CE: 40%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003707
LC-ESI-ITFT; MS2; CE: 40%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003207
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003708
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003208
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003709
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003209
Neoxaline
12 spectra
C23H25N5O4
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
435.19070
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003797
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003317
LC-ESI-ITFT; MS2; CE: 20%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003798
LC-ESI-ITFT; MS2; CE: 20%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003318
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003799
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003319
LC-ESI-ITFT; MS2; CE: 40%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003800
LC-ESI-ITFT; MS2; CE: 40%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003320
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003801
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003321
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003802
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003322
Nivalenol
8 spectra
C15H20O7
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
312.12091
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M-H]-
MSBNK-HBM4EU-HB002964
LC-ESI-ITFT; MS2; CE: 20%; R=7500; [M-H]-
MSBNK-HBM4EU-HB002966
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M-H]-
MSBNK-HBM4EU-HB002968
LC-ESI-ITFT; MS2; CE: 40%; R=7500; [M-H]-
MSBNK-HBM4EU-HB002965
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M+H]+
MSBNK-HBM4EU-HB004019
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M-H]-
MSBNK-HBM4EU-HB002967
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M+H]+
MSBNK-HBM4EU-HB004020
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M-H]-
MSBNK-HBM4EU-HB002969
Norlichexanthone
12 spectra
C14H10O5
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
258.05280
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003611
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003099
LC-ESI-ITFT; MS2; CE: 20%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003612
LC-ESI-ITFT; MS2; CE: 20%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003101
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003613
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003103
LC-ESI-ITFT; MS2; CE: 40%; R=7500; [M+H]+
MSBNK-HBM4EU-HB004071
LC-ESI-ITFT; MS2; CE: 40%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003100
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M+H]+
MSBNK-HBM4EU-HB004072
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003102
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M+H]+
MSBNK-HBM4EU-HB004073
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003104
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Copyright © 2006 MassBank Project; 2011
NORMAN Association
; 2021
MassBank Consortium
Responsible:
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