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Compound Name:
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Results :
2,101 Hit.
( 922 - 1,214 Displayed )
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Name
Formula / Structure
ExactMass
ID
ERGOSTEROL
1 spectrum
C28H44O
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
396.33923
EI-B; MS
JP011384
ERGOSTEROL-TRIMETHYLSILYL-ETHER
1 spectrum
C31H52OSi
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
468.37875
EI-B; MS
JP002702
Ergotamine
11 spectra
C33H35N5O5
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
581.26379
LC-ESI-ITFT; MS2; CE: 10; R=17500; [M+H]+
AC000342
LC-ESI-ITFT; MS2; CE: 20; R=17500; [M+H]+
AC000343
LC-ESI-ITFT; MS2; CE: 30; R=17500; [M+H]+
AC000344
LC-ESI-ITFT; MS2; CE: 40; R=17500; [M+H]+
AC000345
LC-ESI-ITFT; MS2; CE: 55; R=17500; [M+H]+
AC000346
LC-ESI-Q; MS; POS; 15 V
WA001650
LC-ESI-Q; MS; POS; 30 V
WA001649
LC-ESI-Q; MS; POS; 45 V
WA001648
LC-ESI-Q; MS; POS; 60 V
WA001647
LC-ESI-Q; MS; POS; 75 V
WA001646
LC-ESI-Q; MS; POS; 90 V
WA001645
Ergovaline
5 spectra
C29H35N5O5
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
533.26379
LC-ESI-ITFT; MS2; CE: 10; R=17500; [M+H]+
AC000327
LC-ESI-ITFT; MS2; CE: 20; R=17500; [M+H]+
AC000328
LC-ESI-ITFT; MS2; CE: 30; R=17500; [M+H]+
AC000329
LC-ESI-ITFT; MS2; CE: 40; R=17500; [M+H]+
AC000330
LC-ESI-ITFT; MS2; CE: 55; R=17500; [M+H]+
AC000331
ERGSTA-4,24(28)-DIEN-3-ONE
1 spectrum
C28H44O
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
396.33923
EI-B; MS
JP009507
Erid-7-Glc, Miscanthoside, 2-(3,4-dihydroxyphenyl)...
2 spectra
C21H22O11
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
450.39600
LC-ESI-QTOF; MS2
PT104180
LC-ESI-QTOF; MS2
PT204180
Erid-7-Glc, Miscanthoside, Pyracanthoside, ((S)-2-...
12 spectra
C21H22O11
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
450.39600
LC-ESI-QQ; MS2
PS041801
LC-ESI-QQ; MS2
PS041802
LC-ESI-QQ; MS2
PS041803
LC-ESI-QQ; MS2
PS041804
LC-ESI-QQ; MS2
PS041805
LC-ESI-QQ; MS2
PS041806
LC-ESI-QQ; MS2
PS041807
LC-ESI-QQ; MS2
PS041808
LC-ESI-QQ; MS2
PS041809
LC-ESI-QQ; MS2
PS041810
LC-ESI-QQ; MS2
PS041811
LC-ESI-QQ; MS2
PS041812
Eriocitrin
1 spectrum
C27H32O15
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
596.53802
LC-ESI-QQ; MS2
PM000317
Eriodictyol
41 spectra
C15H12O6
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
288.06339
LC-ESI-QTOF; MS
BS003467
LC-ESI-QTOF; MS
PR020015
LC-ESI-QTOF; MS2
PR302483
LC-ESI-QTOF; MS2
PR302488
LC-ESI-QTOF; MS2
PR302494
LC-ESI-QTOF; MS2
PR302500
LC-ESI-QTOF; MS2
PR302506
LC-ESI-QTOF; MS2
PR302512
LC-ESI-QTOF; MS2
PR302518
LC-ESI-QTOF; MS2
PR302524
LC-ESI-QTOF; MS2
PR302530
LC-ESI-QTOF; MS2
PR302535
LC-ESI-QTOF; MS2
PR302541
LC-ESI-QTOF; MS2
PR302547
LC-ESI-QTOF; MS2
PR306152
LC-ESI-QTOF; MS2
PR306157
LC-ESI-QTOF; MS2
PR306162
LC-ESI-QTOF; MS2
PR306167
LC-ESI-QTOF; MS2
PR306172
LC-ESI-QTOF; MS2
PR306177
LC-ESI-QTOF; MS2
PR306182
LC-ESI-QTOF; MS2
PR306187
LC-ESI-QTOF; MS2
PR306192
LC-ESI-QTOF; MS2
PR306197
LC-ESI-QTOF; MS2
PR306202
LC-ESI-QTOF; MS2
PR306207
LC-ESI-QTOF; MS2
PR309310
LC-ESI-QTOF; MS2
PR310998
LC-ESI-QTOF; MS2; CE:10 eV; [M-H]-
BS003463
LC-ESI-QTOF; MS2; CE:20 eV; [M-H]-
BS003464
LC-ESI-QTOF; MS2; CE:30 eV; [2M-H]-
PR040014
LC-ESI-QTOF; MS2; CE:30 eV; [M+H]+
PR040015
LC-ESI-QTOF; MS2; CE:30 eV; [M-H]-
BS003465
LC-ESI-QTOF; MS2; CE:30 eV; [M-H]-
PR040013
LC-ESI-QTOF; MS2; CE:40 eV; [M-H]-
BS003468
LC-ESI-QTOF; MS2; CE:Ramp 5-60 eV; [2M-H]-
PR040012
LC-ESI-QTOF; MS2; CE:Ramp 5-60 eV; [M+H]+
PR040016
LC-ESI-QTOF; MS2; CE:Ramp 5-60 eV; [M-H]-
PR040011
LC-ESI-QTOF; MS2; CE:Ramp 5-60 V; [M+H]+
PR100226
LC-ESI-QTOF; MS2; CE:Ramp 5-60 V; [M-H]-
PR100639
LC-ESI-QTOF; MS; CE:10 eV; [M-H]-
BS003466
Eriodictyol-7-neohesperidoside
7 spectra
C27H32O15
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
596.17407
LC-ESI-QTOF; MS
BS003515
LC-ESI-QTOF; MS2; CE:10 eV; [M-H]-
BS003513
LC-ESI-QTOF; MS2; CE:20 eV; [M-H]-
BS003512
LC-ESI-QTOF; MS2; CE:30 eV; [M-H]-
BS003514
LC-ESI-QTOF; MS2; CE:40 eV; [M-H]-
BS003516
LC-ESI-QTOF; MS2; CE:50 eV; [M-H]-
BS003510
LC-ESI-QTOF; MS; CE:10 eV; [M-H]-
BS003511
Eriodictyol-7-O-glucoside
35 spectra
C21H22O11
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
450.11621
LC-ESI-QTOF; MS
PR020041
LC-ESI-QTOF; MS2
PR302481
LC-ESI-QTOF; MS2
PR302486
LC-ESI-QTOF; MS2
PR302492
LC-ESI-QTOF; MS2
PR302498
LC-ESI-QTOF; MS2
PR302504
LC-ESI-QTOF; MS2
PR302510
LC-ESI-QTOF; MS2
PR302516
LC-ESI-QTOF; MS2
PR302522
LC-ESI-QTOF; MS2
PR302528
LC-ESI-QTOF; MS2
PR302533
LC-ESI-QTOF; MS2
PR302539
LC-ESI-QTOF; MS2
PR302545
LC-ESI-QTOF; MS2
PR306150
LC-ESI-QTOF; MS2
PR306155
LC-ESI-QTOF; MS2
PR306160
LC-ESI-QTOF; MS2
PR306165
LC-ESI-QTOF; MS2
PR306170
LC-ESI-QTOF; MS2
PR306175
LC-ESI-QTOF; MS2
PR306180
LC-ESI-QTOF; MS2
PR306185
LC-ESI-QTOF; MS2
PR306190
LC-ESI-QTOF; MS2
PR306195
LC-ESI-QTOF; MS2
PR306200
LC-ESI-QTOF; MS2
PR306205
LC-ESI-QTOF; MS2
PR309235
LC-ESI-QTOF; MS2
PR310485
LC-ESI-QTOF; MS2; CE:30 V; [2M-H]-
PR040090
LC-ESI-QTOF; MS2; CE:30 V; [M+H]+
PR040091
LC-ESI-QTOF; MS2; CE:30 V; [M-H]-
PR040089
LC-ESI-QTOF; MS2; CE:Ramp 5-60 V; [2M-H]-
PR040088
LC-ESI-QTOF; MS2; CE:Ramp 5-60 V; [M+H]+
PR040092
LC-ESI-QTOF; MS2; CE:Ramp 5-60 V; [M+H]+
PR100239
LC-ESI-QTOF; MS2; CE:Ramp 5-60 V; [M-H]-
PR040087
LC-ESI-QTOF; MS2; CE:Ramp 5-60 V; [M-H]-
PR100655
Eriodictyol-7-O-neohesperidoside
26 spectra
C27H32O15
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
596.53802
LC-ESI-QTOF; MS2
PR302409
LC-ESI-QTOF; MS2
PR302415
LC-ESI-QTOF; MS2
PR302421
LC-ESI-QTOF; MS2
PR302427
LC-ESI-QTOF; MS2
PR302433
LC-ESI-QTOF; MS2
PR302439
LC-ESI-QTOF; MS2
PR302445
LC-ESI-QTOF; MS2
PR302451
LC-ESI-QTOF; MS2
PR302457
LC-ESI-QTOF; MS2
PR302463
LC-ESI-QTOF; MS2
PR302469
LC-ESI-QTOF; MS2
PR302475
LC-ESI-QTOF; MS2
PR306078
LC-ESI-QTOF; MS2
PR306084
LC-ESI-QTOF; MS2
PR306090
LC-ESI-QTOF; MS2
PR306096
LC-ESI-QTOF; MS2
PR306102
LC-ESI-QTOF; MS2
PR306108
LC-ESI-QTOF; MS2
PR306114
LC-ESI-QTOF; MS2
PR306120
LC-ESI-QTOF; MS2
PR306126
LC-ESI-QTOF; MS2
PR306132
LC-ESI-QTOF; MS2
PR306137
LC-ESI-QTOF; MS2
PR306143
LC-ESI-QTOF; MS2
PR308795
LC-ESI-QTOF; MS2
PR310488
Eriodictyol-7-O-rutinoside
25 spectra
C27H32O15
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
596.53802
LC-ESI-QTOF; MS2
PR302480
LC-ESI-QTOF; MS2
PR302485
LC-ESI-QTOF; MS2
PR302491
LC-ESI-QTOF; MS2
PR302497
LC-ESI-QTOF; MS2
PR302503
LC-ESI-QTOF; MS2
PR302509
LC-ESI-QTOF; MS2
PR302515
LC-ESI-QTOF; MS2
PR302521
LC-ESI-QTOF; MS2
PR302527
LC-ESI-QTOF; MS2
PR302538
LC-ESI-QTOF; MS2
PR302544
LC-ESI-QTOF; MS2
PR306149
LC-ESI-QTOF; MS2
PR306154
LC-ESI-QTOF; MS2
PR306159
LC-ESI-QTOF; MS2
PR306164
LC-ESI-QTOF; MS2
PR306169
LC-ESI-QTOF; MS2
PR306174
LC-ESI-QTOF; MS2
PR306179
LC-ESI-QTOF; MS2
PR306184
LC-ESI-QTOF; MS2
PR306189
LC-ESI-QTOF; MS2
PR306194
LC-ESI-QTOF; MS2
PR306199
LC-ESI-QTOF; MS2
PR306204
LC-ESI-QTOF; MS2
PR308796
LC-ESI-QTOF; MS2
PR310489
Erucamide
5 spectra
C22H43NO
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
337.33447
LC-ESI-QTOF; MS2; [M+H]+; CE: 10eV
FIO00882
LC-ESI-QTOF; MS2; [M+H]+; CE: 20eV
FIO00883
LC-ESI-QTOF; MS2; [M+H]+; CE: 30eV
FIO00884
LC-ESI-QTOF; MS2; [M+H]+; CE: 40eV
FIO00885
LC-ESI-QTOF; MS2; [M+H]+; CE: 50eV
FIO00886
ERUCIC ACID TRIMETHYLSILYL ESTER
1 spectrum
C25H50O2Si
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
410.35800
EI-B; MS
JP000586
Erucifoline
40 spectra
C18H23NO6
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
349.15250
LC-ESI-ITFT; MS2; CE: 10%; R=15000; [M+H]+
NA000426
LC-ESI-ITFT; MS2; CE: 100%; R=15000; [M+H]+
NA000717
LC-ESI-ITFT; MS2; CE: 105%; R=15000; [M+H]+
NA000754
LC-ESI-ITFT; MS2; CE: 110%; R=15000; [M+H]+
NA000719
LC-ESI-ITFT; MS2; CE: 115%; R=15000; [M+H]+
NA000756
LC-ESI-ITFT; MS2; CE: 120%; R=15000; [M+H]+
NA000721
LC-ESI-ITFT; MS2; CE: 125%; R=15000; [M+H]+
NA000758
LC-ESI-ITFT; MS2; CE: 15%; R=15000; [M+H]+
NA000427
LC-ESI-ITFT; MS2; CE: 15%; R=15000; [M+H]+
NA000476
LC-ESI-ITFT; MS2; CE: 20%; R=15000; [M+H]+
NA000428
LC-ESI-ITFT; MS2; CE: 20%; R=15000; [M+H]+
NA000477
LC-ESI-ITFT; MS2; CE: 25%; R=15000; [M+H]+
NA000429
LC-ESI-ITFT; MS2; CE: 25%; R=15000; [M+H]+
NA000478
LC-ESI-ITFT; MS2; CE: 30%; R=15000; [M+H]+
NA000430
LC-ESI-ITFT; MS2; CE: 30%; R=15000; [M+H]+
NA000479
LC-ESI-ITFT; MS2; CE: 35%; R=15000; [M+H]+
NA000480
LC-ESI-ITFT; MS2; CE: 35%; R=15000; [M+H]+
NA000527
LC-ESI-ITFT; MS2; CE: 40%; R=15000; [M+H]+
NA000526
LC-ESI-ITFT; MS2; CE: 40%; R=15000; [M+H]+
NA000577
LC-ESI-ITFT; MS2; CE: 45%; R=15000; [M+H]+
NA000529
LC-ESI-ITFT; MS2; CE: 45%; R=15000; [M+H]+
NA000576
LC-ESI-ITFT; MS2; CE: 50%; R=15000; [M+H]+
NA000528
LC-ESI-ITFT; MS2; CE: 50%; R=15000; [M+H]+
NA000579
LC-ESI-ITFT; MS2; CE: 55%; R=15000; [M+H]+
NA000578
LC-ESI-ITFT; MS2; CE: 55%; R=15000; [M+H]+
NA000627
LC-ESI-ITFT; MS2; CE: 60%; R=15000; [M+H]+
NA000530
LC-ESI-ITFT; MS2; CE: 60%; R=15000; [M+H]+
NA000673
LC-ESI-ITFT; MS2; CE: 65%; R=15000; [M+H]+
NA000580
LC-ESI-ITFT; MS2; CE: 65%; R=15000; [M+H]+
NA000629
LC-ESI-ITFT; MS2; CE: 70%; R=15000; [M+H]+
NA000626
LC-ESI-ITFT; MS2; CE: 70%; R=15000; [M+H]+
NA000675
LC-ESI-ITFT; MS2; CE: 75%; R=15000; [M+H]+
NA000672
LC-ESI-ITFT; MS2; CE: 75%; R=15000; [M+H]+
NA000718
LC-ESI-ITFT; MS2; CE: 80%; R=15000; [M+H]+
NA000628
LC-ESI-ITFT; MS2; CE: 80%; R=15000; [M+H]+
NA000755
LC-ESI-ITFT; MS2; CE: 85%; R=15000; [M+H]+
NA000674
LC-ESI-ITFT; MS2; CE: 85%; R=15000; [M+H]+
NA000720
LC-ESI-ITFT; MS2; CE: 90%; R=15000; [M+H]+
NA000630
LC-ESI-ITFT; MS2; CE: 90%; R=15000; [M+H]+
NA000757
LC-ESI-ITFT; MS2; CE: 95%; R=15000; [M+H]+
NA000676
Erythromycin
52 spectra
C37H67NO13
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
733.46124
LC-ESI-ITFT; MS2; CE 35 eV; [M+H]+
CE000001
LC-ESI-ITFT; MS2; CE 45 eV; [M+H]+
CE000002
LC-ESI-ITFT; MS2; CE 55 eV; [M+H]+
CE000003
LC-ESI-ITFT; MS2; CE 70 eV; [M+H]+
CE000004
LC-ESI-ITFT; MS2; CE: 15%; R=15000; [M+H]+
EA018908
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M+H]+
EA018902
LC-ESI-ITFT; MS2; CE: 30%; R=15000; [M+H]+
EA018909
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M+H]+
EA018903
LC-ESI-ITFT; MS2; CE: 35%; R=15000; [M+H]+
EA018914
LC-ESI-ITFT; MS2; CE: 35%; R=7500; [M+H]+
EA018901
LC-ESI-ITFT; MS2; CE: 45%; R=15000; [M+H]+
EA018910
LC-ESI-ITFT; MS2; CE: 45%; R=7500; [M+H]+
EA018904
LC-ESI-ITFT; MS2; CE: 60%; R=15000; [M+H]+
EA018911
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M+H]+
EA018905
LC-ESI-ITFT; MS2; CE: 75%; R=15000; [M+H]+
EA018912
LC-ESI-ITFT; MS2; CE: 75%; R=7500; [M+H]+
EA018906
LC-ESI-ITFT; MS2; CE: 90%; R=15000; [M+H]+
EA018913
LC-ESI-ITFT; MS2; CE: 90%; R=7500; [M+H]+
EA018907
LC-ESI-ITFT; MS; [M+H]+; isotope pattern
CE000005
LC-ESI-Q; MS; NEG; 30 V
WA002287
LC-ESI-Q; MS; POS; 15 V
WA002286
LC-ESI-Q; MS; POS; 30 V
WA002285
LC-ESI-Q; MS; POS; 45 V
WA002284
LC-ESI-Q; MS; POS; 60 V
WA002283
LC-ESI-Q; MS; POS; 75 V
WA002282
LC-ESI-Q; MS; POS; 90 V
WA002281
LC-ESI-QQQ; MS2; Frag=135.0V CID@10.0; [M+H]+
NGA01646
LC-ESI-QQQ; MS2; Frag=135.0V CID@10.0; [M+HCOO]-
NGA04307
LC-ESI-QQQ; MS2; Frag=135.0V CID@15.0; [M+H]+
NGA01647
LC-ESI-QQQ; MS2; Frag=135.0V CID@15.0; [M+HCOO]-
NGA04306
LC-ESI-QQQ; MS2; Frag=135.0V CID@25.0; [M+H]+
NGA01648
LC-ESI-QQQ; MS2; Frag=135.0V CID@25.0; [M+HCOO]-
NGA04305
LC-ESI-QQQ; MS2; Frag=135.0V CID@5.0; [M+H]+
NGA01645
LC-ESI-QQQ; MS2; Frag=135.0V CID@5.0; [M+HCOO]-
NGA04308
LC-ESI-QQQ; MS; [M+H]+
CB000347
LC-ESI-QTOF; MS2; CE: 10 eV; R=35000; [M+H]+
AU105401
LC-ESI-QTOF; MS2; CE: 20 eV; R=35000; [M+H]+
AU105402
LC-ESI-QTOF; MS2; CE: 30 eV; R=35000; [M+H]+
AU105403
LC-ESI-QTOF; MS2; CE: 40 eV; R=35000; [M+H]+
AU105404
LC-ESI-QTOF; MS2; CE: 50 eV; R=35000; [M+H]+
AU105405
LC-ESI-QTOF; MS2; CE: Ramp 30.5-45.7 eV; R=35000; [M+H]+
AU105406
LC-ESI-QTOF; MS2; CE:10 eV; [M+H]+
PB005801
LC-ESI-QTOF; MS2; CE:15 eV; [M+H]+
PB005802
LC-ESI-QTOF; MS2; CE:20 eV; [M+H]+
PB005803
LC-ESI-QTOF; MS2; CE:30 eV; [M+H]+
PB005804
LC-ESI-QTOF; MS2; HILIC; CE: 10 eV; R=35000; [M+H]+
AU105407
LC-ESI-QTOF; MS2; HILIC; CE: 20 eV; R=35000; [M+H]+
AU105408
LC-ESI-QTOF; MS2; HILIC; CE: 30 eV; R=35000; [M+H]+
AU105409
LC-ESI-QTOF; MS2; HILIC; CE: 40 eV; R=35000; [M+H]+
AU105410
LC-ESI-QTOF; MS2; HILIC; CE: 50 eV; R=35000; [M+H]+
AU105411
LC-ESI-QTOF; MS; NEGATIVE
BML81201
LC-ESI-QTOF; MS; POSITIVE
BML81200
erythromycin ethylsuccinate
3 spectra
C43H75NO16
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
861.50861
LC-APCI-QTOF; MS; NEGATIVE
BML81208
LC-ESI-QTOF; MS; NEGATIVE
BML81206
LC-ESI-QTOF; MS; POSITIVE
BML81205
Erythromycin propionate
5 spectra
C40H71NO14
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
790.01019
LC-ESI-QQQ; MS2; Frag=135.0V CID@10.0; [M+H]+
NGA02219
LC-ESI-QQQ; MS2; Frag=135.0V CID@15.0; [M+H]+
NGA02218
LC-ESI-QQQ; MS2; Frag=135.0V CID@25.0; [M+H]+
NGA02217
LC-ESI-QQQ; MS2; Frag=135.0V CID@5.0; [M+H]+
NGA02220
LC-ESI-QQQ; MS; [M+H]+
CB000349
Eschscholtzxanthin
1 spectrum
C40H54O2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
566.41235
FAB-EBEB; MS2; m/z: 566.41; [M]+*
CA000055
Esculentic acid
1 spectrum
C30H48O5
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
488.71411
LC-ESI-QQQ; MS; [M+H]+
CB000471
Esculetin
8 spectra
C9H6O4
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
178.02661
LC-APCI-QTOF; MS; NEGATIVE
BML81213
LC-APCI-QTOF; MS; POSITIVE
BML81212
LC-ESI-QTOF; MS2; CE 10 ev; [M+H]+
BML01641
LC-ESI-QTOF; MS2; CE 10 ev; [M-H]-
BML01674
LC-ESI-QTOF; MS2; CE 20 ev; [M+H]+
BML01652
LC-ESI-QTOF; MS2; CE 20 ev; [M-H]-
BML01684
LC-ESI-QTOF; MS; NEGATIVE
BML81211
LC-ESI-QTOF; MS; POSITIVE
BML81210
esculetin
2 spectra
C9H6O4
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
178.02660
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M+H]+
ML003901
LC-ESI-ITFT; MS2; CE: 50%; R=7500; [M-H]-
ML003951
Esculetin, Esculin aglycon, Cichorigenin, 6,7-Dihy...
1 spectrum
C9H6O4
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
178.14301
LC-ESI-QTOF; MS2
PT112500
Esculetin, Esculin aglycon, Cichorigenin, 6,7-Dihy...
6 spectra
C9H6O4
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
178.14301
LC-ESI-QQ; MS2
PS125001
LC-ESI-QQ; MS2
PS125002
LC-ESI-QQ; MS2
PS125003
LC-ESI-QQ; MS2
PS125007
LC-ESI-QQ; MS2
PS125008
LC-ESI-QQ; MS2
PS125009
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