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Compound Name:
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2,087 Hit.
( 1 - 190 Displayed )
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Name
Formula / Structure
ExactMass
ID
H-shaped caldarchaeol
1 spectrum
C86H170O6
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
1299.29968
FAB-B; MS
MSBNK-UOEH-UO000017
H-shaped caldarchaeol alcohol
1 spectrum
C80H162O4
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
1187.24731
FAB-B; MS
MSBNK-UOEH-UO000020
H-shaped caldarchaeol alcohol tetraacetate
2 spectra
C88H170O8
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
1355.28955
CI-B; MS
MSBNK-UOEH-UO000022
EI-B; MS
MSBNK-UOEH-UO000023
H-shaped caldarchaeol diacetate
1 spectrum
C90H174O8
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
1383.32092
FAB-B; MS
MSBNK-UOEH-UO000019
Habanolide
2 spectra
C15H26O2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
238.19328
LC-ESI-QTOF; MS2; CE: 10 eV; R=35000; [M+H]+
MSBNK-Athens_Univ-AU245601
LC-ESI-QTOF; MS2; CE: Ramp 19.4-29.1 eV; R=35000; [M+H]+
MSBNK-Athens_Univ-AU245606
HALFORDIN
1 spectrum
C14H12O6
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
276.06339
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP003113
HALFORDIN (14-CD3)
1 spectrum
C14H12O6
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
276.06339
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP003117
HALFORDININ
1 spectrum
C18H18O6
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
330.11035
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP003116
HALKENDIN
2 spectra
C13H10O5
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
246.05283
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP003115
EI-B; MS
MSBNK-Fac_Eng_Univ_Tokyo-JP003123
Halocynthiaxanthin
3 spectra
C40H54O4
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
598.40222
FAB-EBEB; MS2; m/z: 598.40; [M]+*
MSBNK-Kyoto_Univ-CA000060
LC-ESI-QTOF; MS2; POSITIVE; [M+H]+; CID; CE 20 V
MSBNK-MSSJ-MSJ00210
LC-ESI-QTOF; MS; POSITIVE; ESI
MSBNK-MSSJ-MSJ00209
Halocynthiaxanthin acetate
1 spectrum
C42H56O5
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
640.41278
FAB-EBEB; MS2; m/z: 640.41; [M]+*
MSBNK-Kyoto_Univ-CA000061
Halofenozide
12 spectra
C18H19ClN2O2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
330.11349
LC-ESI-QFT; MS2; CE: 15; R=17500; [M+H]+
MSBNK-LCSB-LU086301
LC-ESI-QFT; MS2; CE: 15; R=17500; [M-H]-
MSBNK-LCSB-LU086351
LC-ESI-QFT; MS2; CE: 30; R=17500; [M+H]+
MSBNK-LCSB-LU086302
LC-ESI-QFT; MS2; CE: 30; R=17500; [M-H]-
MSBNK-LCSB-LU086352
LC-ESI-QFT; MS2; CE: 45; R=17500; [M+H]+
MSBNK-LCSB-LU086303
LC-ESI-QFT; MS2; CE: 45; R=17500; [M-H]-
MSBNK-LCSB-LU086353
LC-ESI-QFT; MS2; CE: 60; R=17500; [M+H]+
MSBNK-LCSB-LU086304
LC-ESI-QFT; MS2; CE: 60; R=17500; [M-H]-
MSBNK-LCSB-LU086354
LC-ESI-QFT; MS2; CE: 75; R=17500; [M+H]+
MSBNK-LCSB-LU086305
LC-ESI-QFT; MS2; CE: 75; R=17500; [M-H]-
MSBNK-LCSB-LU086355
LC-ESI-QFT; MS2; CE: 90; R=17500; [M+H]+
MSBNK-LCSB-LU086306
LC-ESI-QFT; MS2; CE: 90; R=17500; [M-H]-
MSBNK-LCSB-LU086356
Haloperidol
25 spectra
C21H23ClFNO2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
375.14014
LC-ESI-Q; MS; POS; 15 V, 30 V
MSBNK-Waters-WA002247
LC-ESI-Q; MS; POS; 45 V
MSBNK-Waters-WA002251
LC-ESI-Q; MS; POS; 60 V
MSBNK-Waters-WA002248
LC-ESI-Q; MS; POS; 75 V
MSBNK-Waters-WA002250
LC-ESI-Q; MS; POS; 90 V
MSBNK-Waters-WA002249
LC-ESI-QFT; MS2; CE: 120; R=35000; [M+H]+
MSBNK-Eawag-EQ356607
LC-ESI-QFT; MS2; CE: 150; R=35000; [M+H]+
MSBNK-Eawag-EQ356608
LC-ESI-QFT; MS2; CE: 15; R=17500; [M+H]+
MSBNK-LCSB-LU058801
LC-ESI-QFT; MS2; CE: 15; R=35000; [M+H]+
MSBNK-Eawag-EQ356601
LC-ESI-QFT; MS2; CE: 180; R=35000; [M+H]+
MSBNK-Eawag-EQ356609
LC-ESI-QFT; MS2; CE: 30; R=17500; [M+H]+
MSBNK-LCSB-LU058802
LC-ESI-QFT; MS2; CE: 30; R=35000; [M+H]+
MSBNK-Eawag-EQ356602
LC-ESI-QFT; MS2; CE: 45; R=17500; [M+H]+
MSBNK-LCSB-LU058803
LC-ESI-QFT; MS2; CE: 45; R=35000; [M+H]+
MSBNK-Eawag-EQ356603
LC-ESI-QFT; MS2; CE: 60; R=17500; [M+H]+
MSBNK-LCSB-LU058804
LC-ESI-QFT; MS2; CE: 60; R=35000; [M+H]+
MSBNK-Eawag-EQ356604
LC-ESI-QFT; MS2; CE: 75; R=17500; [M+H]+
MSBNK-LCSB-LU058805
LC-ESI-QFT; MS2; CE: 75; R=35000; [M+H]+
MSBNK-Eawag-EQ356605
LC-ESI-QFT; MS2; CE: 90; R=17500; [M+H]+
MSBNK-LCSB-LU058806
LC-ESI-QFT; MS2; CE: 90; R=35000; [M+H]+
MSBNK-Eawag-EQ356606
LC-ESI-QTOF; MS2; CE: 10 eV; R=35000; [M+H]+
MSBNK-Athens_Univ-AU112201
LC-ESI-QTOF; MS2; CE: 20 eV; R=35000; [M+H]+
MSBNK-Athens_Univ-AU112202
LC-ESI-QTOF; MS2; CE: 30 eV; R=35000; [M+H]+
MSBNK-Athens_Univ-AU112203
LC-ESI-QTOF; MS2; CE: 40 eV; R=35000; [M+H]+
MSBNK-Athens_Univ-AU112204
LC-ESI-QTOF; MS2; CE: 50 eV; R=35000; [M+H]+
MSBNK-Athens_Univ-AU112205
Haloxyfop
34 spectra
C15H11ClF3NO4
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
361.03287
LC-ESI-QFT; MS2; CE: 120; R=35000; [M+H]+
MSBNK-Eawag-EQ356207
LC-ESI-QFT; MS2; CE: 120; R=35000; [M-H]-
MSBNK-Eawag-EQ356257
LC-ESI-QFT; MS2; CE: 150; R=35000; [M+H]+
MSBNK-Eawag-EQ356208
LC-ESI-QFT; MS2; CE: 150; R=35000; [M-H]-
MSBNK-Eawag-EQ356258
LC-ESI-QFT; MS2; CE: 15; R=17500; [M+H]+
MSBNK-LCSB-LU038401
LC-ESI-QFT; MS2; CE: 15; R=17500; [M-H]-
MSBNK-LCSB-LU038451
LC-ESI-QFT; MS2; CE: 15; R=35000; [M+H]+
MSBNK-Eawag-EQ356201
LC-ESI-QFT; MS2; CE: 15; R=35000; [M-H]-
MSBNK-Eawag-EQ356251
LC-ESI-QFT; MS2; CE: 180; R=35000; [M+H]+
MSBNK-Eawag-EQ356209
LC-ESI-QFT; MS2; CE: 180; R=35000; [M-H]-
MSBNK-Eawag-EQ356259
LC-ESI-QFT; MS2; CE: 30; R=17500; [M+H]+
MSBNK-LCSB-LU038402
LC-ESI-QFT; MS2; CE: 30; R=17500; [M-H]-
MSBNK-LCSB-LU038452
LC-ESI-QFT; MS2; CE: 30; R=35000; [M+H]+
MSBNK-Eawag-EQ356202
LC-ESI-QFT; MS2; CE: 30; R=35000; [M-H]-
MSBNK-Eawag-EQ356252
LC-ESI-QFT; MS2; CE: 45; R=17500; [M+H]+
MSBNK-LCSB-LU038403
LC-ESI-QFT; MS2; CE: 45; R=17500; [M-H]-
MSBNK-LCSB-LU038453
LC-ESI-QFT; MS2; CE: 45; R=35000; [M+H]+
MSBNK-Eawag-EQ356203
LC-ESI-QFT; MS2; CE: 45; R=35000; [M-H]-
MSBNK-Eawag-EQ356253
LC-ESI-QFT; MS2; CE: 60; R=17500; [M+H]+
MSBNK-LCSB-LU038404
LC-ESI-QFT; MS2; CE: 60; R=17500; [M-H]-
MSBNK-LCSB-LU038454
LC-ESI-QFT; MS2; CE: 60; R=35000; [M+H]+
MSBNK-Eawag-EQ356204
LC-ESI-QFT; MS2; CE: 60; R=35000; [M-H]-
MSBNK-Eawag-EQ356254
LC-ESI-QFT; MS2; CE: 75; R=17500; [M+H]+
MSBNK-LCSB-LU038405
LC-ESI-QFT; MS2; CE: 75; R=17500; [M-H]-
MSBNK-LCSB-LU038455
LC-ESI-QFT; MS2; CE: 75; R=35000; [M+H]+
MSBNK-Eawag-EQ356205
LC-ESI-QFT; MS2; CE: 75; R=35000; [M-H]-
MSBNK-Eawag-EQ356255
LC-ESI-QFT; MS2; CE: 90; R=17500; [M+H]+
MSBNK-LCSB-LU038406
LC-ESI-QFT; MS2; CE: 90; R=17500; [M-H]-
MSBNK-LCSB-LU038456
LC-ESI-QFT; MS2; CE: 90; R=35000; [M+H]+
MSBNK-Eawag-EQ356206
LC-ESI-QFT; MS2; CE: 90; R=35000; [M-H]-
MSBNK-Eawag-EQ356256
LC-ESI-QQ; MS2; CE:10 V; [M+H]+
MSBNK-Waters-WA000235
LC-ESI-QQ; MS2; CE:20 V; [M+H]+
MSBNK-Waters-WA000236
LC-ESI-QQ; MS2; CE:30 V; [M+H]+
MSBNK-Waters-WA000237
LC-ESI-QQ; MS2; CE:40 V; [M+H]+
MSBNK-Waters-WA000238
Haplamidine
4 spectra
C20H22N2O2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
322.41049
LC-ESI-QQQ; MS2; Frag=135.0V CID@10.0; [M+H]+
MSBNK-RIKEN_NPDepo-NGA02962
LC-ESI-QQQ; MS2; Frag=135.0V CID@15.0; [M+H]+
MSBNK-RIKEN_NPDepo-NGA02963
LC-ESI-QQQ; MS2; Frag=135.0V CID@25.0; [M+H]+
MSBNK-RIKEN_NPDepo-NGA02964
LC-ESI-QQQ; MS2; Frag=135.0V CID@5.0; [M+H]+
MSBNK-RIKEN_NPDepo-NGA02961
Haploperoside C
5 spectra
C22H28O13
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
500.15298
LC-ESI-QTOF; MS2; CE 10 ev; [M+H]+
MSBNK-Washington_State_Univ-BML01534
LC-ESI-QTOF; MS2; CE 20 ev; [M+H]+
MSBNK-Washington_State_Univ-BML01546
LC-ESI-QTOF; MS2; CE 40 ev; [M+H]+
MSBNK-Washington_State_Univ-BML01558
LC-ESI-QTOF; MS; NEGATIVE
MSBNK-Washington_State_Univ-BML81331
LC-ESI-QTOF; MS; POSITIVE
MSBNK-Washington_State_Univ-BML81330
Haploperoside C Acetate
8 spectra
C34H40O19
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
752.21637
LC-APCI-QTOF; MS; NEGATIVE
MSBNK-Washington_State_Univ-BML81338
LC-APCI-QTOF; MS; POSITIVE
MSBNK-Washington_State_Univ-BML81337
LC-ESI-QTOF; MS2; CE 10 ev; [M+CH3COOH-H]-
MSBNK-Washington_State_Univ-BML01681
LC-ESI-QTOF; MS2; CE 10 ev; [M+H]+
MSBNK-Washington_State_Univ-BML01648
LC-ESI-QTOF; MS2; CE 20 ev; [M+H]+
MSBNK-Washington_State_Univ-BML01659
LC-ESI-QTOF; MS2; CE 40 ev; [M+H]+
MSBNK-Washington_State_Univ-BML01670
LC-ESI-QTOF; MS; NEGATIVE
MSBNK-Washington_State_Univ-BML81336
LC-ESI-QTOF; MS; POSITIVE
MSBNK-Washington_State_Univ-BML81335
Haploperozide
5 spectra
C28H38O17
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
646.21088
LC-ESI-QTOF; MS2; CE 10 ev; [M+H]+
MSBNK-Washington_State_Univ-BML01535
LC-ESI-QTOF; MS2; CE 20 ev; [M+H]+
MSBNK-Washington_State_Univ-BML01547
LC-ESI-QTOF; MS2; CE 40 ev; [M+H]+
MSBNK-Washington_State_Univ-BML01559
LC-ESI-QTOF; MS; NEGATIVE
MSBNK-Washington_State_Univ-BML81341
LC-ESI-QTOF; MS; POSITIVE
MSBNK-Washington_State_Univ-BML81340
Haplophyllidine
5 spectra
C18H23NO4
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
317.38831
LC-ESI-QQQ; MS2; Frag=135.0V CID@10.0; [M+H]+
MSBNK-RIKEN_NPDepo-NGA00434
LC-ESI-QQQ; MS2; Frag=135.0V CID@15.0; [M+H]+
MSBNK-RIKEN_NPDepo-NGA00435
LC-ESI-QQQ; MS2; Frag=135.0V CID@25.0; [M+H]+
MSBNK-RIKEN_NPDepo-NGA00436
LC-ESI-QQQ; MS2; Frag=135.0V CID@5.0; [M+H]+
MSBNK-RIKEN_NPDepo-NGA00433
LC-ESI-QQQ; MS; [M+H]+
MSBNK-RIKEN_NPDepo-CB000014
haploside D
8 spectra
C30H34O18
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
682.17450
LC-ESI-QTOF; MS2; CE 10 ev; [M+H]+
MSBNK-Washington_State_Univ-BML01590
LC-ESI-QTOF; MS2; CE 10 ev; [M-H]-
MSBNK-Washington_State_Univ-BML01617
LC-ESI-QTOF; MS2; CE 20 ev; [M+H]+
MSBNK-Washington_State_Univ-BML01599
LC-ESI-QTOF; MS2; CE 20 ev; [M-H]-
MSBNK-Washington_State_Univ-BML01625
LC-ESI-QTOF; MS2; CE 40 ev; [M+H]+
MSBNK-Washington_State_Univ-BML01608
LC-ESI-QTOF; MS2; CE 40 ev; [M-H]-
MSBNK-Washington_State_Univ-BML01633
LC-ESI-QTOF; MS; NEGATIVE
MSBNK-Washington_State_Univ-BML81346
LC-ESI-QTOF; MS; POSITIVE
MSBNK-Washington_State_Univ-BML81345
Harmaline
29 spectra
C13H14N2O
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
214.11061
GC-EI-TOF; MS; 1 TMS; BP:174
MSBNK-Kazusa-KZ000213
GC-EI-TOF; MS; 1 TMS; BP:174
MSBNK-RIKEN-PR010121
LC-APCI-QTOF; MS; NEGATIVE
MSBNK-Washington_State_Univ-BML81353
LC-APCI-QTOF; MS; POSITIVE
MSBNK-Washington_State_Univ-BML81352
LC-ESI-IT; MS2; m/z: 215; [M+H]+
MSBNK-Keio_Univ-KO008994
LC-ESI-IT; MS3; m/z: 215/174; [M+H]+
MSBNK-Keio_Univ-KO008997
LC-ESI-IT; MS3; m/z: 215/198; [M+H]+
MSBNK-Keio_Univ-KO008996
LC-ESI-IT; MS3; m/z: 215/200; [M+H]+
MSBNK-Keio_Univ-KO008995
LC-ESI-QQ; MS2; CE:10 V; [M+H]+
MSBNK-Keio_Univ-KO003098
LC-ESI-QQ; MS2; CE:10 V; [M-H]-
MSBNK-Keio_Univ-KO001018
LC-ESI-QQ; MS2; CE:20 V; [M+H]+
MSBNK-Keio_Univ-KO003099
LC-ESI-QQ; MS2; CE:20 V; [M-H]-
MSBNK-Keio_Univ-KO001019
LC-ESI-QQ; MS2; CE:30 V; [M+H]+
MSBNK-Keio_Univ-KO003100
LC-ESI-QQ; MS2; CE:30 V; [M-H]-
MSBNK-Keio_Univ-KO001020
LC-ESI-QQ; MS2; CE:40 V; [M+H]+
MSBNK-Keio_Univ-KO003101
LC-ESI-QQ; MS2; CE:40 V; [M-H]-
MSBNK-Keio_Univ-KO001021
LC-ESI-QQ; MS2; CE:50 V; [M+H]+
MSBNK-Keio_Univ-KO003102
LC-ESI-QQ; MS2; CE:50 V; [M-H]-
MSBNK-Keio_Univ-KO001022
LC-ESI-QTOF; MS2; CE 10 ev; [M+H]+
MSBNK-Washington_State_Univ-BML00065
LC-ESI-QTOF; MS2; CE 10 ev; [M-H]-
MSBNK-Washington_State_Univ-BML00090
LC-ESI-QTOF; MS2; CE 20 ev; [M+H]+
MSBNK-Washington_State_Univ-BML00072
LC-ESI-QTOF; MS2; CE 20 ev; [M-H]-
MSBNK-Washington_State_Univ-BML00086
LC-ESI-QTOF; MS2; CE 40 ev; [M+H]+
MSBNK-Washington_State_Univ-BML00079
LC-ESI-QTOF; MS2; CE 40 ev; [M-H]-
MSBNK-Washington_State_Univ-BML00094
LC-ESI-QTOF; MS2; CE:30 V; [M+H]+
MSBNK-RIKEN-PR100070
LC-ESI-QTOF; MS2; CE:Ramp 5-60 V; [M+H]+
MSBNK-RIKEN-PR100069
LC-ESI-QTOF; MS2; CE:Ramp 5-60 V; [M-H]-
MSBNK-RIKEN-PR100517
LC-ESI-QTOF; MS; NEGATIVE
MSBNK-Washington_State_Univ-BML81351
LC-ESI-QTOF; MS; POSITIVE
MSBNK-Washington_State_Univ-BML81350
Harmaline hydrochloride dihydrate, 1-Methyl-7-meth...
4 spectra
C13H14N2O
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
214.26801
LC-ESI-QQ; MS2
MSBNK-RIKEN_ReSpect-PS012501
LC-ESI-QQ; MS2
MSBNK-RIKEN_ReSpect-PS012502
LC-ESI-QQ; MS2
MSBNK-RIKEN_ReSpect-PS012503
LC-ESI-QQ; MS2
MSBNK-RIKEN_ReSpect-PS012504
Harmaline hydrochloride dihydrate, 7-methoxy-1-met...
3 spectra
C13H14N2O
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
214.26801
LC-ESI-QTOF; MS2
MSBNK-RIKEN_ReSpect-PT101250
LC-ESI-QTOF; MS2
MSBNK-RIKEN_ReSpect-PT101253
LC-ESI-QTOF; MS2
MSBNK-RIKEN_ReSpect-PT201250
Harmalol
30 spectra
C12H12N2O
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
200.09496
LC-APCI-QTOF; MS; NEGATIVE
MSBNK-Washington_State_Univ-BML81358
LC-APCI-QTOF; MS; POSITIVE
MSBNK-Washington_State_Univ-BML81357
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR300545
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR300550
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR300554
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR300559
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR300563
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR300568
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR300573
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR300577
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR300581
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR300586
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR300591
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR300595
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR304783
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR304785
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR304787
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR304789
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR304791
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR304793
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR304795
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR304797
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR304799
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR304801
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR304803
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR304805
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR308855
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR310551
LC-ESI-QTOF; MS; NEGATIVE
MSBNK-Washington_State_Univ-BML81356
LC-ESI-QTOF; MS; POSITIVE
MSBNK-Washington_State_Univ-BML81355
HARMAN
2 spectra
C12H10N2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
182.08440
ESI-ITFT; MS2; CE: 35%; R=30000; [M+H]+
MSBNK-UFZ-UA000701
ESI-ITFT; MS2; CE: 35%; R=30000; [M-H]-
MSBNK-UFZ-UA000702
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