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4,225 Hit.
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Results End
Name
Formula / Structure
ExactMass
ID
nPFOA
5 spectra
C8HF15O2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
413.97369
LC-ESI-QQ; MS2; CE10eV
FFF00342
LC-ESI-QQ; MS2; CE20eV
FFF00343
LC-ESI-QQ; MS2; CE30eV
FFF00344
LC-ESI-QQ; MS2; CE40eV
FFF00345
LC-ESI-QQ; MS2; CE50eV
FFF00346
nPFOS
6 spectra
C8HF17O3S
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
499.93750
LC-ESI-QQ; MS2; CE10eV; [M-H]-
FFF00293
LC-ESI-QQ; MS2; CE20eV; [M-H]-
FFF00294
LC-ESI-QQ; MS2; CE30eV; [M-H]-
FFF00295
LC-ESI-QQ; MS2; CE40eV; [M-H]-
FFF00296
LC-ESI-QQ; MS2; CE50eV; [M-H]-
FFF00297
LC-ESI-QQ; MS2; CE60eV; [M-H]-
FFF00298
Nuarimol
12 spectra
C17H12ClFN2O
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
314.06219
LC-ESI-QFT; MS2; CE: 15; R=17500; [M+H]+
LU124401
LC-ESI-QFT; MS2; CE: 15; R=17500; [M-H]-
LU124451
LC-ESI-QFT; MS2; CE: 30; R=17500; [M+H]+
LU124402
LC-ESI-QFT; MS2; CE: 30; R=17500; [M-H]-
LU124452
LC-ESI-QFT; MS2; CE: 45; R=17500; [M+H]+
LU124403
LC-ESI-QFT; MS2; CE: 45; R=17500; [M-H]-
LU124453
LC-ESI-QFT; MS2; CE: 60; R=17500; [M+H]+
LU124404
LC-ESI-QFT; MS2; CE: 60; R=17500; [M-H]-
LU124454
LC-ESI-QFT; MS2; CE: 75; R=17500; [M+H]+
LU124405
LC-ESI-QFT; MS2; CE: 75; R=17500; [M-H]-
LU124455
LC-ESI-QFT; MS2; CE: 90; R=17500; [M+H]+
LU124406
LC-ESI-QFT; MS2; CE: 90; R=17500; [M-H]-
LU124456
Nucleocardyl, Sandesin, 9-beta-D-Ribofuranosyladen...
3 spectra
C10H13N5O4
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
267.24500
LC-ESI-QTOF; MS2
PT100400
LC-ESI-QTOF; MS2
PT100403
LC-ESI-QTOF; MS2
PT200400
Nucleocardyl, Sandesin, 9-beta-D-Ribofuranosyladen...
6 spectra
C10H13N5O4
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
267.24500
LC-ESI-QQ; MS2
PS004001
LC-ESI-QQ; MS2
PS004002
LC-ESI-QQ; MS2
PS004003
LC-ESI-QQ; MS2
PS004004
LC-ESI-QQ; MS2
PS004005
LC-ESI-QQ; MS2
PS004006
Nudicauline
5 spectra
C38H50N2O11
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
710.82898
LC-ESI-QQQ; MS2; Frag=135.0V CID@10.0; [M+H]+
NGA02007
LC-ESI-QQQ; MS2; Frag=135.0V CID@15.0; [M+H]+
NGA02006
LC-ESI-QQQ; MS2; Frag=135.0V CID@25.0; [M+H]+
NGA02005
LC-ESI-QQQ; MS2; Frag=135.0V CID@5.0; [M+H]+
NGA02008
LC-ESI-QQQ; MS; [M+H]+
CB000205
Nva, L-2-Aminovaleric acid, (S)-2-Aminovaleric aci...
2 spectra
C5H11NO2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
117.14800
LC-ESI-QTOF; MS2
PT102840
LC-ESI-QTOF; MS2
PT202840
Nva, L-2-Aminovaleric acid, (S)-2-Aminovaleric aci...
4 spectra
C5H11NO2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
117.14800
LC-ESI-QQ; MS2
PS028401
LC-ESI-QQ; MS2
PS028402
LC-ESI-QQ; MS2
PS028403
LC-ESI-QQ; MS2
PS028404
NVE_247.1330_17.3
6 spectra
C15H18O3
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
246.12560
LC-ESI-QFT; MS2; CE: 15; R=17500; [M+H]+
ET120601
LC-ESI-QFT; MS2; CE: 30; R=17500; [M+H]+
ET120602
LC-ESI-QFT; MS2; CE: 45; R=17500; [M+H]+
ET120603
LC-ESI-QFT; MS2; CE: 60; R=17500; [M+H]+
ET120604
LC-ESI-QFT; MS2; CE: 75; R=17500; [M+H]+
ET120605
LC-ESI-QFT; MS2; CE: 90; R=17500; [M+H]+
ET120606
NVE_250.1804_10.8
5 spectra
C15H23NO2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
249.17290
LC-ESI-QFT; MS2; CE: 15-90; R=17500; [M+H]+
ET120101
LC-ESI-QFT; MS2; CE: 15-90; R=17500; [M+H]+
ET120102
LC-ESI-QFT; MS2; CE: 15-90; R=17500; [M+H]+
ET120103
LC-ESI-QFT; MS2; CE: 15-90; R=17500; [M+H]+
ET120104
LC-ESI-QFT; MS2; CE: 15-90; R=17500; [M+H]+
ET120105
NVE_264.1959_12.6
5 spectra
C16H25NO2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
263.18851
LC-ESI-QFT; MS2; CE: 15-90; R=17500; [M+H]+
ET120001
LC-ESI-QFT; MS2; CE: 15-90; R=17500; [M+H]+
ET120002
LC-ESI-QFT; MS2; CE: 15-90; R=17500; [M+H]+
ET120003
LC-ESI-QFT; MS2; CE: 15-90; R=17500; [M+H]+
ET120004
LC-ESI-QFT; MS2; CE: 15-90; R=17500; [M+H]+
ET120005
NVE_274.1802_16.6
6 spectra
C17H23NO2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
273.17291
LC-ESI-QFT; MS2; CE: 15; R=17500; [M+H]+
ET120701
LC-ESI-QFT; MS2; CE: 30; R=17500; [M+H]+
ET120702
LC-ESI-QFT; MS2; CE: 45; R=17500; [M+H]+
ET120703
LC-ESI-QFT; MS2; CE: 60; R=17500; [M+H]+
ET120704
LC-ESI-QFT; MS2; CE: 75; R=17500; [M+H]+
ET120705
LC-ESI-QFT; MS2; CE: 90; R=17500; [M+H]+
ET120706
NVE_278.1753_15.6
1 spectrum
C16H23NO3
277.16779
LC-ESI-QFT; MS2; CE: (160-0.41mz or 15) NCE; R=17500; [M+H]+
ET121103
NVE_278.1753_8.8
6 spectra
C16H23NO3
277.16779
LC-ESI-QFT; MS2; CE: 15; R=17500; [M+H]+
ET121001
LC-ESI-QFT; MS2; CE: 30; R=17500; [M+H]+
ET121002
LC-ESI-QFT; MS2; CE: 45; R=17500; [M+H]+
ET121003
LC-ESI-QFT; MS2; CE: 60; R=17500; [M+H]+
ET121004
LC-ESI-QFT; MS2; CE: 75; R=17500; [M+H]+
ET121005
LC-ESI-QFT; MS2; CE: 90; R=17500; [M+H]+
ET121006
NVE_278.1753_9.6
6 spectra
C16H23NO3
277.16779
LC-ESI-QFT; MS2; CE: 15; R=17500; [M+H]+
ET120501
LC-ESI-QFT; MS2; CE: 30; R=17500; [M+H]+
ET120502
LC-ESI-QFT; MS2; CE: 45; R=17500; [M+H]+
ET120503
LC-ESI-QFT; MS2; CE: 60; R=17500; [M+H]+
ET120504
LC-ESI-QFT; MS2; CE: 75; R=17500; [M+H]+
ET120505
LC-ESI-QFT; MS2; CE: 90; R=17500; [M+H]+
ET120506
NVE_280.1909_11.8
6 spectra
C16H25NO3
279.18341
LC-ESI-QFT; MS2; CE: 15; R=17500; [M+H]+
ET120401
LC-ESI-QFT; MS2; CE: 30; R=17500; [M+H]+
ET120402
LC-ESI-QFT; MS2; CE: 45; R=17500; [M+H]+
ET120403
LC-ESI-QFT; MS2; CE: 60; R=17500; [M+H]+
ET120404
LC-ESI-QFT; MS2; CE: 75; R=17500; [M+H]+
ET120405
LC-ESI-QFT; MS2; CE: 90; R=17500; [M+H]+
ET120406
Nw-Acetylhistamine
10 spectra
C7H11N3O
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
153.09021
LC-ESI-QQ; MS2; CE:10 V; [M+H]+
KO002233
LC-ESI-QQ; MS2; CE:10 V; [M-H]-
KO000161
LC-ESI-QQ; MS2; CE:20 V; [M+H]+
KO002234
LC-ESI-QQ; MS2; CE:20 V; [M-H]-
KO000162
LC-ESI-QQ; MS2; CE:30 V; [M+H]+
KO002235
LC-ESI-QQ; MS2; CE:30 V; [M-H]-
KO000163
LC-ESI-QQ; MS2; CE:40 V; [M+H]+
KO002236
LC-ESI-QQ; MS2; CE:40 V; [M-H]-
KO000164
LC-ESI-QQ; MS2; CE:50 V; [M+H]+
KO002237
LC-ESI-QQ; MS2; CE:50 V; [M-H]-
KO000165
Nw-Methyltryptamine
5 spectra
C11H14N2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
174.11571
LC-ESI-QQ; MS2; CE:10 V; [M+H]+
KO003497
LC-ESI-QQ; MS2; CE:20 V; [M+H]+
KO003498
LC-ESI-QQ; MS2; CE:30 V; [M+H]+
KO003499
LC-ESI-QQ; MS2; CE:40 V; [M+H]+
KO003500
LC-ESI-QQ; MS2; CE:50 V; [M+H]+
KO003501
NX2 toxin
10 spectra
C17H24O6
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
324.15729
LC-APCI-ITFT; MS2; CE: 10; R=17500; [M+H]+
AC000392
LC-APCI-ITFT; MS2; CE: 10; R=17500; [M-H2O+H]+
AC000397
LC-APCI-ITFT; MS2; CE: 20; R=17500; [M+H]+
AC000393
LC-APCI-ITFT; MS2; CE: 20; R=17500; [M-H2O+H]+
AC000398
LC-APCI-ITFT; MS2; CE: 30; R=17500; [M+H]+
AC000394
LC-APCI-ITFT; MS2; CE: 30; R=17500; [M-H2O+H]+
AC000399
LC-APCI-ITFT; MS2; CE: 40; R=17500; [M+H]+
AC000395
LC-APCI-ITFT; MS2; CE: 40; R=17500; [M-H2O+H]+
AC000400
LC-APCI-ITFT; MS2; CE: 55; R=17500; [M+H]+
AC000396
LC-APCI-ITFT; MS2; CE: 55; R=17500; [M-H2O+H]+
AC000401
Nylidrin
121 spectra
C19H25NO2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
299.18851
ESI-QTOF; MS2; CE: 10eV; R=15000; [M+H]+
HB002720
ESI-QTOF; MS2; CE: 15eV; R=15000; [M+H]+
HB002721
ESI-QTOF; MS2; CE: 20eV; R=15000; [M+H]+
HB002722
ESI-QTOF; MS2; CE: 25eV; R=15000; [M+H]+
HB002723
ESI-QTOF; MS2; CE: 30eV; R=15000; [M+H]+
HB002724
ESI-QTOF; MS2; CE: 35eV; R=15000; [M+H]+
HB002725
ESI-QTOF; MS2; CE: 40eV; R=15000; [M+H]+
HB002726
ESI-QTOF; MS2; CE: 45eV; R=15000; [M+H]+
HB002727
ESI-QTOF; MS2; CE: 50eV; R=15000; [M+H]+
HB002729
ESI-QTOF; MS2; CE: 5eV; R=15000; [M+H]+
HB002728
LC-ESI-ITFT; MS2; CE: 10%; R=15000; [M+H]+
HB000201
LC-ESI-ITFT; MS2; CE: 10%; R=7500; [M+H]+
HB002394
LC-ESI-ITFT; MS2; CE: 100%; R=15000; [M+H]+
HB000231
LC-ESI-ITFT; MS2; CE: 100%; R=15000; [M+H]+
HB000247
LC-ESI-ITFT; MS2; CE: 105%; R=15000; [M+H]+
HB000236
LC-ESI-ITFT; MS2; CE: 105%; R=15000; [M+H]+
HB000244
LC-ESI-ITFT; MS2; CE: 110%; R=15000; [M+H]+
HB000233
LC-ESI-ITFT; MS2; CE: 110%; R=15000; [M+H]+
HB000249
LC-ESI-ITFT; MS2; CE: 115%; R=15000; [M+H]+
HB000238
LC-ESI-ITFT; MS2; CE: 115%; R=15000; [M+H]+
HB000252
LC-ESI-ITFT; MS2; CE: 120%; R=15000; [M+H]+
HB000235
LC-ESI-ITFT; MS2; CE: 120%; R=15000; [M+H]+
HB000257
LC-ESI-ITFT; MS2; CE: 125%; R=15000; [M+H]+
HB000240
LC-ESI-ITFT; MS2; CE: 125%; R=15000; [M+H]+
HB000254
LC-ESI-ITFT; MS2; CE: 130%; R=15000; [M+H]+
HB000241
LC-ESI-ITFT; MS2; CE: 130%; R=15000; [M+H]+
HB000259
LC-ESI-ITFT; MS2; CE: 135%; R=15000; [M+H]+
HB000246
LC-ESI-ITFT; MS2; CE: 140%; R=15000; [M+H]+
HB000243
LC-ESI-ITFT; MS2; CE: 145%; R=15000; [M+H]+
HB000248
LC-ESI-ITFT; MS2; CE: 15%; R=15000; [M+H]+
HB000202
LC-ESI-ITFT; MS2; CE: 15%; R=15000; [M+H]+
HB000206
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M+H]+
HB002395
LC-ESI-ITFT; MS2; CE: 150%; R=15000; [M+H]+
HB000245
LC-ESI-ITFT; MS2; CE: 155%; R=15000; [M+H]+
HB000250
LC-ESI-ITFT; MS2; CE: 160%; R=15000; [M+H]+
HB000251
LC-ESI-ITFT; MS2; CE: 165%; R=15000; [M+H]+
HB000256
LC-ESI-ITFT; MS2; CE: 170%; R=15000; [M+H]+
HB000253
LC-ESI-ITFT; MS2; CE: 175%; R=15000; [M+H]+
HB000258
LC-ESI-ITFT; MS2; CE: 180%; R=15000; [M+H]+
HB000255
LC-ESI-ITFT; MS2; CE: 185%; R=15000; [M+H]+
HB000260
LC-ESI-ITFT; MS2; CE: 20%; R=15000; [M+H]+
HB000203
LC-ESI-ITFT; MS2; CE: 20%; R=15000; [M+H]+
HB000207
LC-ESI-ITFT; MS2; CE: 20%; R=7500; [M+H]+
HB002396
LC-ESI-ITFT; MS2; CE: 25%; R=15000; [M+H]+
HB000208
LC-ESI-ITFT; MS2; CE: 25%; R=7500; [M+H]+
HB002397
LC-ESI-ITFT; MS2; CE: 30%; R=15000; [M+H]+
HB000205
LC-ESI-ITFT; MS2; CE: 30%; R=15000; [M+H]+
HB000209
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M+H]+
HB002398
LC-ESI-ITFT; MS2; CE: 35%; R=15000; [M+H]+
HB000204
LC-ESI-ITFT; MS2; CE: 35%; R=15000; [M+H]+
HB000210
LC-ESI-ITFT; MS2; CE: 35%; R=15000; [M+H]+
HB000212
LC-ESI-ITFT; MS2; CE: 35%; R=7500; [M+H]+
HB002399
LC-ESI-ITFT; MS2; CE: 40%; R=15000; [M+H]+
HB000211
LC-ESI-ITFT; MS2; CE: 40%; R=15000; [M+H]+
HB000217
LC-ESI-ITFT; MS2; CE: 40%; R=7500; [M+H]+
HB002400
LC-ESI-ITFT; MS2; CE: 45%; R=15000; [M+H]+
HB000214
LC-ESI-ITFT; MS2; CE: 45%; R=15000; [M+H]+
HB000216
LC-ESI-ITFT; MS2; CE: 45%; R=7500; [M+H]+
HB002401
LC-ESI-ITFT; MS2; CE: 5%; R=7500; [M+H]+
HB002402
LC-ESI-ITFT; MS2; CE: 50%; R=15000; [M+H]+
HB000213
LC-ESI-ITFT; MS2; CE: 50%; R=15000; [M+H]+
HB000219
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M+H]+
HB002403
LC-ESI-ITFT; MS2; CE: 55%; R=15000; [M+H]+
HB000218
LC-ESI-ITFT; MS2; CE: 55%; R=15000; [M+H]+
HB000222
LC-ESI-ITFT; MS2; CE: 55%; R=7500; [M+H]+
HB002404
LC-ESI-ITFT; MS2; CE: 60%; R=15000; [M+H]+
HB000215
LC-ESI-ITFT; MS2; CE: 60%; R=15000; [M+H]+
HB000227
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M+H]+
HB002405
LC-ESI-ITFT; MS2; CE: 65%; R=15000; [M+H]+
HB000220
LC-ESI-ITFT; MS2; CE: 65%; R=15000; [M+H]+
HB000224
LC-ESI-ITFT; MS2; CE: 65%; R=7500; [M+H]+
HB002406
LC-ESI-ITFT; MS2; CE: 70%; R=15000; [M+H]+
HB000221
LC-ESI-ITFT; MS2; CE: 70%; R=15000; [M+H]+
HB000229
LC-ESI-ITFT; MS2; CE: 70%; R=7500; [M+H]+
HB002407
LC-ESI-ITFT; MS2; CE: 75%; R=15000; [M+H]+
HB000226
LC-ESI-ITFT; MS2; CE: 75%; R=15000; [M+H]+
HB000232
LC-ESI-ITFT; MS2; CE: 75%; R=7500; [M+H]+
HB002408
LC-ESI-ITFT; MS2; CE: 80%; R=15000; [M+H]+
HB000223
LC-ESI-ITFT; MS2; CE: 80%; R=15000; [M+H]+
HB000237
LC-ESI-ITFT; MS2; CE: 80%; R=7500; [M+H]+
HB002409
LC-ESI-ITFT; MS2; CE: 85%; R=15000; [M+H]+
HB000228
LC-ESI-ITFT; MS2; CE: 85%; R=15000; [M+H]+
HB000234
LC-ESI-ITFT; MS2; CE: 90%; R=15000; [M+H]+
HB000225
LC-ESI-ITFT; MS2; CE: 90%; R=15000; [M+H]+
HB000239
LC-ESI-ITFT; MS2; CE: 95%; R=15000; [M+H]+
HB000230
LC-ESI-ITFT; MS2; CE: 95%; R=15000; [M+H]+
HB000242
LC-ESI-QFT; MS2; CE: 10%; R=17500; [M+H]+
HB002171
LC-ESI-QFT; MS2; CE: 10%; R=30000; [M+H]+
HB002001
LC-ESI-QFT; MS2; CE: 15%; R=17500; [M+H]+
HB002172
LC-ESI-QFT; MS2; CE: 20%; R=17500; [M+H]+
HB002173
LC-ESI-QFT; MS2; CE: 20%; R=30000; [M+H]+
HB002002
LC-ESI-QFT; MS2; CE: 25%; R=17500; [M+H]+
HB002174
LC-ESI-QFT; MS2; CE: 30%; R=17500; [M+H]+
HB002175
LC-ESI-QFT; MS2; CE: 35%; R=17500; [M+H]+
HB002176
LC-ESI-QFT; MS2; CE: 40%; R=17500; [M+H]+
HB002177
LC-ESI-QFT; MS2; CE: 40%; R=30000; [M+H]+
HB002003
LC-ESI-QFT; MS2; CE: 45%; R=17500; [M+H]+
HB002178
LC-ESI-QFT; MS2; CE: 50%; R=17500; [M+H]+
HB002179
LC-ESI-QFT; MS2; CE: 55%; R=17500; [M+H]+
HB002180
LC-ESI-QFT; MS2; CE: 60%; R=17500; [M+H]+
HB002181
LC-ESI-QFT; MS2; CE: 65%; R=17500; [M+H]+
HB002182
LC-ESI-QFT; MS2; CE: 70%; R=17500; [M+H]+
HB002183
LC-ESI-QFT; MS2; CE: 75%; R=17500; [M+H]+
HB002184
LC-ESI-QFT; MS2; CE: 80%; R=17500; [M+H]+
HB002185
LC-ESI-QFT; MS2; CE: 80%; R=30000; [M+H]+
HB002004
LC-ESI-QFT; MS2; CE: CE15; R=17500; [M+H]+
HB002785
LC-ESI-QFT; MS2; CE: CE30; R=17500; [M+H]+
HB002786
LC-ESI-QFT; MS2; CE: CE45; R=17500; [M+H]+
HB002787
LC-ESI-QFT; MS2; CE: CE60; R=17500; [M+H]+
HB002788
LC-ESI-QFT; MS2; CE: CE75; R=17500; [M+H]+
HB002789
LC-ESI-QFT; MS2; CE: CE90; R=17500; [M+H]+
HB002790
LC-ESI-QTOF; MS2; CE: 10 eV; R=3600; [M+H]+
HB002570
LC-ESI-QTOF; MS2; CE: 15 eV; R=3600; [M+H]+
HB002571
LC-ESI-QTOF; MS2; CE: 20 eV; R=3600; [M+H]+
HB002572
LC-ESI-QTOF; MS2; CE: 25 eV; R=3600; [M+H]+
HB002573
LC-ESI-QTOF; MS2; CE: 30 eV; R=3600; [M+H]+
HB002574
LC-ESI-QTOF; MS2; CE: 35 eV; R=3600; [M+H]+
HB002575
LC-ESI-QTOF; MS2; CE: 40 eV; R=3600; [M+H]+
HB002576
LC-ESI-QTOF; MS2; CE: 45 eV; R=3600; [M+H]+
HB002577
LC-ESI-QTOF; MS2; CE: 5 eV; R=3600; [M+H]+
HB002579
LC-ESI-QTOF; MS2; CE: 50 eV; R=3600; [M+H]+
HB002578
Nystatin
12 spectra
C47H75NO17
Generated by the Chemistry Development Kit (http://github.com/cdk)
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925.50348
LC-ESI-QFT; MS2; CE: 15; R=35000; [M+H]+
EQ314001
LC-ESI-QFT; MS2; CE: 15; R=35000; [M-H]-
EQ314051
LC-ESI-QFT; MS2; CE: 30; R=35000; [M+H]+
EQ314002
LC-ESI-QFT; MS2; CE: 30; R=35000; [M-H]-
EQ314052
LC-ESI-QFT; MS2; CE: 45; R=35000; [M+H]+
EQ314003
LC-ESI-QFT; MS2; CE: 45; R=35000; [M-H]-
EQ314053
LC-ESI-QFT; MS2; CE: 60; R=35000; [M+H]+
EQ314004
LC-ESI-QFT; MS2; CE: 60; R=35000; [M-H]-
EQ314054
LC-ESI-QFT; MS2; CE: 75; R=35000; [M+H]+
EQ314005
LC-ESI-QFT; MS2; CE: 75; R=35000; [M-H]-
EQ314055
LC-ESI-QFT; MS2; CE: 90; R=35000; [M+H]+
EQ314006
LC-ESI-QFT; MS2; CE: 90; R=35000; [M-H]-
EQ314056
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