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Name
Formula / Structure
ExactMass
ID
Roquefortine E
6 spectra
C27H31N5O2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
457.24777
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003162
LC-ESI-ITFT; MS2; CE: 20%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003163
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003164
LC-ESI-ITFT; MS2; CE: 40%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003165
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003166
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003167
Rubratoxin A
6 spectra
C26H32O11
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
520.19446
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003210
LC-ESI-ITFT; MS2; CE: 20%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003211
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003212
LC-ESI-ITFT; MS2; CE: 40%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003213
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003214
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003215
Rubrofusarin
12 spectra
C15H12O5
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
272.06851
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003585
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003075
LC-ESI-ITFT; MS2; CE: 20%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003586
LC-ESI-ITFT; MS2; CE: 20%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003076
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003587
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003077
LC-ESI-ITFT; MS2; CE: 40%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003588
LC-ESI-ITFT; MS2; CE: 40%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003078
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003589
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003079
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003590
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003080
Rugulosin
12 spectra
C30H22O10
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
542.12128
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003713
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003216
LC-ESI-ITFT; MS2; CE: 20%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003714
LC-ESI-ITFT; MS2; CE: 20%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003217
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003715
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003218
LC-ESI-ITFT; MS2; CE: 40%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003716
LC-ESI-ITFT; MS2; CE: 40%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003219
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003717
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003220
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003718
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003221
Rugulotrosin A
12 spectra
C32H30O14
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
638.16357
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003719
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003222
LC-ESI-ITFT; MS2; CE: 20%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003720
LC-ESI-ITFT; MS2; CE: 20%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003223
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003721
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003224
LC-ESI-ITFT; MS2; CE: 40%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003722
LC-ESI-ITFT; MS2; CE: 40%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003225
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003723
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003226
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003724
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003227
Skyrin
12 spectra
C30H18O10
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
538.09003
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003882
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003413
LC-ESI-ITFT; MS2; CE: 20%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003883
LC-ESI-ITFT; MS2; CE: 20%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003414
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003884
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003415
LC-ESI-ITFT; MS2; CE: 40%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003885
LC-ESI-ITFT; MS2; CE: 40%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003416
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003886
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003417
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003887
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003418
Stachybotrylactam
12 spectra
C23H31NO4
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
385.22531
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003864
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003392
LC-ESI-ITFT; MS2; CE: 20%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003865
LC-ESI-ITFT; MS2; CE: 20%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003393
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003866
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003394
LC-ESI-ITFT; MS2; CE: 40%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003867
LC-ESI-ITFT; MS2; CE: 40%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003395
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003868
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003396
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003869
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003397
Sulfamethoxazole
115 spectra
C10H11N3O3S
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
253.05209
ESI-QTOF; MS2; CE: 10eV; R=15000; [M+H]+
MSBNK-HBM4EU-HB002749
ESI-QTOF; MS2; CE: 15eV; R=15000; [M+H]+
MSBNK-HBM4EU-HB002750
ESI-QTOF; MS2; CE: 20eV; R=15000; [M+H]+
MSBNK-HBM4EU-HB002751
ESI-QTOF; MS2; CE: 25eV; R=15000; [M+H]+
MSBNK-HBM4EU-HB002752
ESI-QTOF; MS2; CE: 30eV; R=15000; [M+H]+
MSBNK-HBM4EU-HB002753
ESI-QTOF; MS2; CE: 35eV; R=15000; [M+H]+
MSBNK-HBM4EU-HB002754
ESI-QTOF; MS2; CE: 40eV; R=15000; [M+H]+
MSBNK-HBM4EU-HB002755
ESI-QTOF; MS2; CE: 45eV; R=15000; [M+H]+
MSBNK-HBM4EU-HB002756
ESI-QTOF; MS2; CE: 50eV; R=15000; [M+H]+
MSBNK-HBM4EU-HB002758
ESI-QTOF; MS2; CE: 5eV; R=15000; [M+H]+
MSBNK-HBM4EU-HB002757
LC-ESI-ITFT; MS2; CE: 10%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001601
LC-ESI-ITFT; MS2; CE: 10%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002437
LC-ESI-ITFT; MS2; CE: 100%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001631
LC-ESI-ITFT; MS2; CE: 100%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001647
LC-ESI-ITFT; MS2; CE: 105%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001636
LC-ESI-ITFT; MS2; CE: 105%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001644
LC-ESI-ITFT; MS2; CE: 110%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001633
LC-ESI-ITFT; MS2; CE: 110%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001649
LC-ESI-ITFT; MS2; CE: 115%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001638
LC-ESI-ITFT; MS2; CE: 115%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001652
LC-ESI-ITFT; MS2; CE: 120%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001635
LC-ESI-ITFT; MS2; CE: 120%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001657
LC-ESI-ITFT; MS2; CE: 125%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001640
LC-ESI-ITFT; MS2; CE: 125%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001654
LC-ESI-ITFT; MS2; CE: 130%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001641
LC-ESI-ITFT; MS2; CE: 130%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001659
LC-ESI-ITFT; MS2; CE: 135%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001646
LC-ESI-ITFT; MS2; CE: 140%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001643
LC-ESI-ITFT; MS2; CE: 145%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001648
LC-ESI-ITFT; MS2; CE: 15%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001602
LC-ESI-ITFT; MS2; CE: 15%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001606
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002438
LC-ESI-ITFT; MS2; CE: 150%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001645
LC-ESI-ITFT; MS2; CE: 155%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001650
LC-ESI-ITFT; MS2; CE: 160%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001651
LC-ESI-ITFT; MS2; CE: 165%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001656
LC-ESI-ITFT; MS2; CE: 170%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001653
LC-ESI-ITFT; MS2; CE: 175%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001658
LC-ESI-ITFT; MS2; CE: 180%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001655
LC-ESI-ITFT; MS2; CE: 185%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001660
LC-ESI-ITFT; MS2; CE: 20%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001603
LC-ESI-ITFT; MS2; CE: 20%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001607
LC-ESI-ITFT; MS2; CE: 20%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002439
LC-ESI-ITFT; MS2; CE: 25%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001608
LC-ESI-ITFT; MS2; CE: 25%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002440
LC-ESI-ITFT; MS2; CE: 30%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001605
LC-ESI-ITFT; MS2; CE: 30%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001609
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002441
LC-ESI-ITFT; MS2; CE: 35%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001604
LC-ESI-ITFT; MS2; CE: 35%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001610
LC-ESI-ITFT; MS2; CE: 35%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001612
LC-ESI-ITFT; MS2; CE: 35%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002442
LC-ESI-ITFT; MS2; CE: 40%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001611
LC-ESI-ITFT; MS2; CE: 40%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001617
LC-ESI-ITFT; MS2; CE: 40%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002443
LC-ESI-ITFT; MS2; CE: 45%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001614
LC-ESI-ITFT; MS2; CE: 45%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001616
LC-ESI-ITFT; MS2; CE: 45%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002444
LC-ESI-ITFT; MS2; CE: 5%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002445
LC-ESI-ITFT; MS2; CE: 50%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001613
LC-ESI-ITFT; MS2; CE: 50%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001619
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002446
LC-ESI-ITFT; MS2; CE: 55%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001618
LC-ESI-ITFT; MS2; CE: 55%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001622
LC-ESI-ITFT; MS2; CE: 55%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002447
LC-ESI-ITFT; MS2; CE: 60%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001615
LC-ESI-ITFT; MS2; CE: 60%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001627
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002448
LC-ESI-ITFT; MS2; CE: 65%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001620
LC-ESI-ITFT; MS2; CE: 65%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001624
LC-ESI-ITFT; MS2; CE: 65%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002449
LC-ESI-ITFT; MS2; CE: 70%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001621
LC-ESI-ITFT; MS2; CE: 70%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001629
LC-ESI-ITFT; MS2; CE: 70%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002450
LC-ESI-ITFT; MS2; CE: 75%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001626
LC-ESI-ITFT; MS2; CE: 75%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001632
LC-ESI-ITFT; MS2; CE: 75%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002451
LC-ESI-ITFT; MS2; CE: 80%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001623
LC-ESI-ITFT; MS2; CE: 80%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001637
LC-ESI-ITFT; MS2; CE: 80%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002452
LC-ESI-ITFT; MS2; CE: 85%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001628
LC-ESI-ITFT; MS2; CE: 85%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001634
LC-ESI-ITFT; MS2; CE: 90%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001625
LC-ESI-ITFT; MS2; CE: 90%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001639
LC-ESI-ITFT; MS2; CE: 95%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001630
LC-ESI-ITFT; MS2; CE: 95%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001642
LC-ESI-QFT; MS2; CE: 10%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002216
LC-ESI-QFT; MS2; CE: 10%; R=30000; [M+H]+
MSBNK-HBM4EU-HB002013
LC-ESI-QFT; MS2; CE: 15%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002217
LC-ESI-QFT; MS2; CE: 20%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002218
LC-ESI-QFT; MS2; CE: 20%; R=30000; [M+H]+
MSBNK-HBM4EU-HB002014
LC-ESI-QFT; MS2; CE: 25%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002219
LC-ESI-QFT; MS2; CE: 30%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002220
LC-ESI-QFT; MS2; CE: 35%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002221
LC-ESI-QFT; MS2; CE: 40%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002222
LC-ESI-QFT; MS2; CE: 40%; R=30000; [M+H]+
MSBNK-HBM4EU-HB002015
LC-ESI-QFT; MS2; CE: 45%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002223
LC-ESI-QFT; MS2; CE: 50%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002224
LC-ESI-QFT; MS2; CE: 55%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002225
LC-ESI-QFT; MS2; CE: 60%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002226
LC-ESI-QFT; MS2; CE: 65%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002227
LC-ESI-QFT; MS2; CE: 70%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002228
LC-ESI-QFT; MS2; CE: 75%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002229
LC-ESI-QFT; MS2; CE: 80%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002230
LC-ESI-QFT; MS2; CE: 80%; R=30000; [M+H]+
MSBNK-HBM4EU-HB002016
LC-ESI-QTOF; MS2; CE: 10 eV; R=3600; [M+H]+
MSBNK-HBM4EU-HB002600
LC-ESI-QTOF; MS2; CE: 15 eV; R=3600; [M+H]+
MSBNK-HBM4EU-HB002601
LC-ESI-QTOF; MS2; CE: 20 eV; R=3600; [M+H]+
MSBNK-HBM4EU-HB002602
LC-ESI-QTOF; MS2; CE: 25 eV; R=3600; [M+H]+
MSBNK-HBM4EU-HB002603
LC-ESI-QTOF; MS2; CE: 30 eV; R=3600; [M+H]+
MSBNK-HBM4EU-HB002604
LC-ESI-QTOF; MS2; CE: 35 eV; R=3600; [M+H]+
MSBNK-HBM4EU-HB002605
LC-ESI-QTOF; MS2; CE: 40 eV; R=3600; [M+H]+
MSBNK-HBM4EU-HB002606
LC-ESI-QTOF; MS2; CE: 45 eV; R=3600; [M+H]+
MSBNK-HBM4EU-HB002607
LC-ESI-QTOF; MS2; CE: 5 eV; R=3600; [M+H]+
MSBNK-HBM4EU-HB002609
LC-ESI-QTOF; MS2; CE: 50 eV; R=3600; [M+H]+
MSBNK-HBM4EU-HB002608
Sulfamoxole
121 spectra
C11H13N3O3S
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
267.06781
ESI-QTOF; MS2; CE: 10eV; R=15000; [M+H]+
MSBNK-HBM4EU-HB002759
ESI-QTOF; MS2; CE: 15eV; R=15000; [M+H]+
MSBNK-HBM4EU-HB002760
ESI-QTOF; MS2; CE: 20eV; R=15000; [M+H]+
MSBNK-HBM4EU-HB002761
ESI-QTOF; MS2; CE: 25eV; R=15000; [M+H]+
MSBNK-HBM4EU-HB002762
ESI-QTOF; MS2; CE: 30eV; R=15000; [M+H]+
MSBNK-HBM4EU-HB002763
ESI-QTOF; MS2; CE: 35eV; R=15000; [M+H]+
MSBNK-HBM4EU-HB002764
ESI-QTOF; MS2; CE: 40eV; R=15000; [M+H]+
MSBNK-HBM4EU-HB002765
ESI-QTOF; MS2; CE: 45eV; R=15000; [M+H]+
MSBNK-HBM4EU-HB002766
ESI-QTOF; MS2; CE: 50eV; R=15000; [M+H]+
MSBNK-HBM4EU-HB002768
ESI-QTOF; MS2; CE: 5eV; R=15000; [M+H]+
MSBNK-HBM4EU-HB002767
LC-ESI-ITFT; MS2; CE: 10%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001701
LC-ESI-ITFT; MS2; CE: 10%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002453
LC-ESI-ITFT; MS2; CE: 100%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001731
LC-ESI-ITFT; MS2; CE: 100%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001747
LC-ESI-ITFT; MS2; CE: 105%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001736
LC-ESI-ITFT; MS2; CE: 105%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001744
LC-ESI-ITFT; MS2; CE: 110%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001733
LC-ESI-ITFT; MS2; CE: 110%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001749
LC-ESI-ITFT; MS2; CE: 115%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001738
LC-ESI-ITFT; MS2; CE: 115%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001752
LC-ESI-ITFT; MS2; CE: 120%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001735
LC-ESI-ITFT; MS2; CE: 120%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001757
LC-ESI-ITFT; MS2; CE: 125%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001740
LC-ESI-ITFT; MS2; CE: 125%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001754
LC-ESI-ITFT; MS2; CE: 130%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001741
LC-ESI-ITFT; MS2; CE: 130%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001759
LC-ESI-ITFT; MS2; CE: 135%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001746
LC-ESI-ITFT; MS2; CE: 140%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001743
LC-ESI-ITFT; MS2; CE: 145%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001748
LC-ESI-ITFT; MS2; CE: 15%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001702
LC-ESI-ITFT; MS2; CE: 15%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001706
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002454
LC-ESI-ITFT; MS2; CE: 150%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001745
LC-ESI-ITFT; MS2; CE: 155%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001750
LC-ESI-ITFT; MS2; CE: 160%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001751
LC-ESI-ITFT; MS2; CE: 165%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001756
LC-ESI-ITFT; MS2; CE: 170%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001753
LC-ESI-ITFT; MS2; CE: 175%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001758
LC-ESI-ITFT; MS2; CE: 180%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001755
LC-ESI-ITFT; MS2; CE: 185%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001760
LC-ESI-ITFT; MS2; CE: 20%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001703
LC-ESI-ITFT; MS2; CE: 20%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001707
LC-ESI-ITFT; MS2; CE: 20%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002455
LC-ESI-ITFT; MS2; CE: 25%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001708
LC-ESI-ITFT; MS2; CE: 25%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002456
LC-ESI-ITFT; MS2; CE: 30%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001705
LC-ESI-ITFT; MS2; CE: 30%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001709
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002457
LC-ESI-ITFT; MS2; CE: 35%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001704
LC-ESI-ITFT; MS2; CE: 35%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001710
LC-ESI-ITFT; MS2; CE: 35%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001712
LC-ESI-ITFT; MS2; CE: 35%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002458
LC-ESI-ITFT; MS2; CE: 40%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001711
LC-ESI-ITFT; MS2; CE: 40%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001717
LC-ESI-ITFT; MS2; CE: 40%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002459
LC-ESI-ITFT; MS2; CE: 45%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001714
LC-ESI-ITFT; MS2; CE: 45%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001716
LC-ESI-ITFT; MS2; CE: 45%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002460
LC-ESI-ITFT; MS2; CE: 5%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002461
LC-ESI-ITFT; MS2; CE: 50%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001713
LC-ESI-ITFT; MS2; CE: 50%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001719
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002462
LC-ESI-ITFT; MS2; CE: 55%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001718
LC-ESI-ITFT; MS2; CE: 55%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001722
LC-ESI-ITFT; MS2; CE: 55%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002463
LC-ESI-ITFT; MS2; CE: 60%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001715
LC-ESI-ITFT; MS2; CE: 60%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001727
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002464
LC-ESI-ITFT; MS2; CE: 65%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001720
LC-ESI-ITFT; MS2; CE: 65%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001724
LC-ESI-ITFT; MS2; CE: 65%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002465
LC-ESI-ITFT; MS2; CE: 70%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001721
LC-ESI-ITFT; MS2; CE: 70%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001729
LC-ESI-ITFT; MS2; CE: 70%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002466
LC-ESI-ITFT; MS2; CE: 75%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001726
LC-ESI-ITFT; MS2; CE: 75%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001732
LC-ESI-ITFT; MS2; CE: 75%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002467
LC-ESI-ITFT; MS2; CE: 80%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001723
LC-ESI-ITFT; MS2; CE: 80%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001737
LC-ESI-ITFT; MS2; CE: 80%; R=7500; [M+H]+
MSBNK-HBM4EU-HB002468
LC-ESI-ITFT; MS2; CE: 85%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001728
LC-ESI-ITFT; MS2; CE: 85%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001734
LC-ESI-ITFT; MS2; CE: 90%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001725
LC-ESI-ITFT; MS2; CE: 90%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001739
LC-ESI-ITFT; MS2; CE: 95%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001730
LC-ESI-ITFT; MS2; CE: 95%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001742
LC-ESI-QFT; MS2; CE: 10%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002231
LC-ESI-QFT; MS2; CE: 10%; R=30000; [M+H]+
MSBNK-HBM4EU-HB002017
LC-ESI-QFT; MS2; CE: 15%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002232
LC-ESI-QFT; MS2; CE: 20%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002233
LC-ESI-QFT; MS2; CE: 20%; R=30000; [M+H]+
MSBNK-HBM4EU-HB002018
LC-ESI-QFT; MS2; CE: 25%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002234
LC-ESI-QFT; MS2; CE: 30%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002235
LC-ESI-QFT; MS2; CE: 35%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002236
LC-ESI-QFT; MS2; CE: 40%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002237
LC-ESI-QFT; MS2; CE: 40%; R=30000; [M+H]+
MSBNK-HBM4EU-HB002019
LC-ESI-QFT; MS2; CE: 45%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002238
LC-ESI-QFT; MS2; CE: 50%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002239
LC-ESI-QFT; MS2; CE: 55%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002240
LC-ESI-QFT; MS2; CE: 60%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002241
LC-ESI-QFT; MS2; CE: 65%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002242
LC-ESI-QFT; MS2; CE: 70%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002243
LC-ESI-QFT; MS2; CE: 75%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002244
LC-ESI-QFT; MS2; CE: 80%; R=17500; [M+H]+
MSBNK-HBM4EU-HB002245
LC-ESI-QFT; MS2; CE: 80%; R=30000; [M+H]+
MSBNK-HBM4EU-HB002020
LC-ESI-QFT; MS2; CE: CE15; R=17500; [M+H]+
MSBNK-HBM4EU-HB002797
LC-ESI-QFT; MS2; CE: CE30; R=17500; [M+H]+
MSBNK-HBM4EU-HB002798
LC-ESI-QFT; MS2; CE: CE45; R=17500; [M+H]+
MSBNK-HBM4EU-HB002799
LC-ESI-QFT; MS2; CE: CE60; R=17500; [M+H]+
MSBNK-HBM4EU-HB002800
LC-ESI-QFT; MS2; CE: CE75; R=17500; [M+H]+
MSBNK-HBM4EU-HB002801
LC-ESI-QFT; MS2; CE: CE90; R=17500; [M+H]+
MSBNK-HBM4EU-HB002802
LC-ESI-QTOF; MS2; CE: 10 eV; R=3600; [M+H]+
MSBNK-HBM4EU-HB002610
LC-ESI-QTOF; MS2; CE: 15 eV; R=3600; [M+H]+
MSBNK-HBM4EU-HB002611
LC-ESI-QTOF; MS2; CE: 20 eV; R=3600; [M+H]+
MSBNK-HBM4EU-HB002612
LC-ESI-QTOF; MS2; CE: 25 eV; R=3600; [M+H]+
MSBNK-HBM4EU-HB002613
LC-ESI-QTOF; MS2; CE: 30 eV; R=3600; [M+H]+
MSBNK-HBM4EU-HB002614
LC-ESI-QTOF; MS2; CE: 35 eV; R=3600; [M+H]+
MSBNK-HBM4EU-HB002615
LC-ESI-QTOF; MS2; CE: 40 eV; R=3600; [M+H]+
MSBNK-HBM4EU-HB002616
LC-ESI-QTOF; MS2; CE: 45 eV; R=3600; [M+H]+
MSBNK-HBM4EU-HB002617
LC-ESI-QTOF; MS2; CE: 5 eV; R=3600; [M+H]+
MSBNK-HBM4EU-HB002619
LC-ESI-QTOF; MS2; CE: 50 eV; R=3600; [M+H]+
MSBNK-HBM4EU-HB002618
Sulochrin
12 spectra
C17H16O7
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
332.08960
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003852
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003380
LC-ESI-ITFT; MS2; CE: 20%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003853
LC-ESI-ITFT; MS2; CE: 20%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003381
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003854
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003382
LC-ESI-ITFT; MS2; CE: 40%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003855
LC-ESI-ITFT; MS2; CE: 40%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003383
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003856
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003384
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003857
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003385
Sulthiame
60 spectra
C10H14N2O4S2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
290.03949
LC-ESI-ITFT; MS2; CE: 10%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001801
LC-ESI-ITFT; MS2; CE: 100%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001831
LC-ESI-ITFT; MS2; CE: 100%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001847
LC-ESI-ITFT; MS2; CE: 105%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001836
LC-ESI-ITFT; MS2; CE: 105%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001844
LC-ESI-ITFT; MS2; CE: 110%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001833
LC-ESI-ITFT; MS2; CE: 110%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001849
LC-ESI-ITFT; MS2; CE: 115%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001838
LC-ESI-ITFT; MS2; CE: 115%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001852
LC-ESI-ITFT; MS2; CE: 120%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001835
LC-ESI-ITFT; MS2; CE: 120%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001857
LC-ESI-ITFT; MS2; CE: 125%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001840
LC-ESI-ITFT; MS2; CE: 125%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001854
LC-ESI-ITFT; MS2; CE: 130%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001841
LC-ESI-ITFT; MS2; CE: 130%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001859
LC-ESI-ITFT; MS2; CE: 135%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001846
LC-ESI-ITFT; MS2; CE: 140%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001843
LC-ESI-ITFT; MS2; CE: 145%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001848
LC-ESI-ITFT; MS2; CE: 15%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001802
LC-ESI-ITFT; MS2; CE: 15%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001806
LC-ESI-ITFT; MS2; CE: 150%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001845
LC-ESI-ITFT; MS2; CE: 155%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001850
LC-ESI-ITFT; MS2; CE: 160%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001851
LC-ESI-ITFT; MS2; CE: 165%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001856
LC-ESI-ITFT; MS2; CE: 170%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001853
LC-ESI-ITFT; MS2; CE: 175%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001858
LC-ESI-ITFT; MS2; CE: 180%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001855
LC-ESI-ITFT; MS2; CE: 185%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001860
LC-ESI-ITFT; MS2; CE: 20%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001803
LC-ESI-ITFT; MS2; CE: 20%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001807
LC-ESI-ITFT; MS2; CE: 25%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001808
LC-ESI-ITFT; MS2; CE: 30%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001805
LC-ESI-ITFT; MS2; CE: 30%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001809
LC-ESI-ITFT; MS2; CE: 35%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001804
LC-ESI-ITFT; MS2; CE: 35%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001810
LC-ESI-ITFT; MS2; CE: 35%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001812
LC-ESI-ITFT; MS2; CE: 40%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001811
LC-ESI-ITFT; MS2; CE: 40%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001817
LC-ESI-ITFT; MS2; CE: 45%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001814
LC-ESI-ITFT; MS2; CE: 45%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001816
LC-ESI-ITFT; MS2; CE: 50%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001813
LC-ESI-ITFT; MS2; CE: 50%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001819
LC-ESI-ITFT; MS2; CE: 55%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001818
LC-ESI-ITFT; MS2; CE: 55%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001822
LC-ESI-ITFT; MS2; CE: 60%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001815
LC-ESI-ITFT; MS2; CE: 60%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001827
LC-ESI-ITFT; MS2; CE: 65%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001820
LC-ESI-ITFT; MS2; CE: 65%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001824
LC-ESI-ITFT; MS2; CE: 70%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001821
LC-ESI-ITFT; MS2; CE: 70%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001829
LC-ESI-ITFT; MS2; CE: 75%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001826
LC-ESI-ITFT; MS2; CE: 75%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001832
LC-ESI-ITFT; MS2; CE: 80%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001823
LC-ESI-ITFT; MS2; CE: 80%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001837
LC-ESI-ITFT; MS2; CE: 85%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001828
LC-ESI-ITFT; MS2; CE: 85%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001834
LC-ESI-ITFT; MS2; CE: 90%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001825
LC-ESI-ITFT; MS2; CE: 90%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001839
LC-ESI-ITFT; MS2; CE: 95%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001830
LC-ESI-ITFT; MS2; CE: 95%; R=15000; [M+H]+
MSBNK-HBM4EU-HB001842
T-2 tetraol
5 spectra
C15H22O6
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
298.14160
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M-H]-
MSBNK-HBM4EU-HB002953
LC-ESI-ITFT; MS2; CE: 20%; R=7500; [M-H]-
MSBNK-HBM4EU-HB002955
LC-ESI-ITFT; MS2; CE: 40%; R=7500; [M-H]-
MSBNK-HBM4EU-HB002954
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M-H]-
MSBNK-HBM4EU-HB002956
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M-H]-
MSBNK-HBM4EU-HB002957
T2 tetraol
2 spectra
C15H22O6
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
298.14160
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003513
LC-ESI-ITFT; MS2; CE: 20%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003514
Tentotoxin
12 spectra
C22H30N4O4
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
414.22672
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003617
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003111
LC-ESI-ITFT; MS2; CE: 20%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003618
LC-ESI-ITFT; MS2; CE: 20%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003112
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003619
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003113
LC-ESI-ITFT; MS2; CE: 40%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003620
LC-ESI-ITFT; MS2; CE: 40%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003114
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003621
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003115
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003622
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003116
Tenuazonic acid
12 spectra
C10H15NO3
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
197.10519
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003614
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003105
LC-ESI-ITFT; MS2; CE: 20%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003615
LC-ESI-ITFT; MS2; CE: 20%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003107
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M+H]+
MSBNK-HBM4EU-HB003616
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003109
LC-ESI-ITFT; MS2; CE: 40%; R=7500; [M+H]+
MSBNK-HBM4EU-HB004074
LC-ESI-ITFT; MS2; CE: 40%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003106
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M+H]+
MSBNK-HBM4EU-HB004075
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003108
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M+H]+
MSBNK-HBM4EU-HB004076
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M-H]-
MSBNK-HBM4EU-HB003110
Terbuthylazine-desaturated (TENTATIVE)
1 spectrum
C9H14ClN5
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
227.09300
LC-ESI-QFT; MS2; CE: 42%; R=70000; [M+H]+
MSBNK-HBM4EU-HB002912
Terbuthylazine-deschloro (PROBABLE)
1 spectrum
C9H17N5O
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
211.14240
LC-ESI-QFT; MS2; CE: 30%; R=70000; [M+H]+
MSBNK-HBM4EU-HB002915
Terbuthylazine-desethyl (PROBABLE)
1 spectrum
C7H12ClN5
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
201.07730
LC-ESI-QFT; MS2; CE: 30%; R=70000; [M+H]+
MSBNK-HBM4EU-HB002911
Terbuthylazine-OH (TENTATIVE)
2 spectra
C9H16ClN5O
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
245.10420
LC-ESI-QFT; MS2; CE: 30%; R=70000; [M+H]+
MSBNK-HBM4EU-HB002913
LC-ESI-QFT; MS2; CE: 30%; R=70000; [M+H]+
MSBNK-HBM4EU-HB002914
Terbutryn-desaturated (TENTATIVE)
3 spectra
C10H17N5S
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
239.11951
LC-ESI-QFT; MS2; CE: 30%; R=70000; [M+H]+
MSBNK-HBM4EU-HB002919
LC-ESI-QFT; MS2; CE: 30%; R=70000; [M+H]+
MSBNK-HBM4EU-HB002920
LC-ESI-QFT; MS2; CE: 55%; R=70000; [M+H]+
MSBNK-HBM4EU-HB002918
Terbutryn-diOH (TENTATIVE)
4 spectra
C10H19N5O2S
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
273.12491
LC-ESI-QFT; MS2; CE: 30%; R=70000; [M+H]+
MSBNK-HBM4EU-HB002921
LC-ESI-QFT; MS2; CE: 30%; R=70000; [M+H]+
MSBNK-HBM4EU-HB002922
LC-ESI-QFT; MS2; CE: 30%; R=70000; [M+H]+
MSBNK-HBM4EU-HB002923
LC-ESI-QFT; MS2; CE: 55%; R=70000; [M+H]+
MSBNK-HBM4EU-HB002924
Terbutryn-OH (TENTATIVE)
4 spectra
C10H19N5OS
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
257.13000
LC-ESI-QFT; MS2; CE: 30%; R=70000; [M+H]+
MSBNK-HBM4EU-HB002925
LC-ESI-QFT; MS2; CE: 55%; R=70000; [M+H]+
MSBNK-HBM4EU-HB002926
LC-ESI-QFT; MS2; CE: 55%; R=70000; [M+H]+
MSBNK-HBM4EU-HB002927
LC-ESI-QFT; MS2; CE: 55%; R=70000; [M+H]+
MSBNK-HBM4EU-HB002928
Terbutryn-OH-desaturated (TENTATIVE)
2 spectra
C10H17N5OS
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
255.11440
LC-ESI-QFT; MS2; CE: 30%; R=70000; [M+H]+
MSBNK-HBM4EU-HB002916
LC-ESI-QFT; MS2; CE: 30%; R=70000; [M+H]+
MSBNK-HBM4EU-HB002917
Terbutryn-OH-desethyl (TENTATIVE)
1 spectrum
C8H15N5S
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
213.10381
LC-ESI-QFT; MS2; CE: 30%; R=70000; [M+H]+
MSBNK-HBM4EU-HB002929
Terbutryn-OH-desmethyl (TENTATIVE)
2 spectra
C9H17N5OS
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
243.11440
LC-ESI-QFT; MS2; CE: 30%; R=70000; [M+H]+
MSBNK-HBM4EU-HB002930
LC-ESI-QFT; MS2; CE: 55%; R=70000; [M+H]+
MSBNK-HBM4EU-HB002931
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