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Compound Name:
F
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2,940 Hit.
( 581 - 675 Displayed )
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Name
Formula / Structure
ExactMass
ID
Feruloyl dehydrotyramine (isomer of 1655)
1 spectrum
C18H17NO4
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
311.33701
LC-ESI-QTOF; MS2
PR311019
Feruloyl Hexoside (isomer of 847)
1 spectrum
C16H20O9
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
356.32700
LC-ESI-QTOF; MS2
PR309327
Feruloyl Hexoside (isomer of 849)
1 spectrum
C16H20O9
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
356.32700
LC-ESI-QTOF; MS2
PR309328
Feruloyl Lactate
1 spectrum
C13H14O7
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
282.24799
LC-ESI-QTOF; MS2
PR309326
Feruloyl lysine
1 spectrum
C16H22N2O5
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
322.36099
LC-ESI-QTOF; MS2
PR311016
Feruloyl O-methyldehydrodopamine
1 spectrum
C19H19NO5
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
341.36301
LC-ESI-QTOF; MS2
PR311022
Feruloyl O-methyldopamine
1 spectrum
C19H21NO5
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
343.37900
LC-ESI-QTOF; MS2
PR311023
Feruloyl putrescine (isomer of 1173)
1 spectrum
C14H20N2O3
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
264.32501
LC-ESI-QTOF; MS2
PR311013
Feruloyl putrescine (isomer of 1178)
1 spectrum
C14H20N2O3
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
264.32501
LC-ESI-QTOF; MS2
PR311012
Feruloyl quinic acid
1 spectrum
C17H20O9
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
368.33801
LC-ESI-QTOF; MS2
PR311017
Feruloyl quinic acid (isomer of 886, 887)
1 spectrum
C17H20O9
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
368.33801
LC-ESI-QTOF; MS2
PR309021
Feruloyl quinic acid (isomer of 886, 888)
1 spectrum
C17H20O9
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
368.33801
LC-ESI-QTOF; MS2
PR309020
Feruloyl quinic acid (isomer of 887, 888)
1 spectrum
C17H20O9
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
368.33801
LC-ESI-QTOF; MS2
PR309019
Feruloyl tyramine
1 spectrum
C18H19NO4
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
313.35300
LC-ESI-QTOF; MS2
PR311020
Feruloylguaiacyl hexoside
1 spectrum
C23H26O11
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
478.45001
LC-ESI-QTOF; MS2
PR309330
Feruloylputrescine
2 spectra
C14H20N2O3
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
264.14740
LC-ESI-ITTOF; MS2; [M+H]+
MSJ00004
LC-ESI-ITTOF; MS; Positive
MSJ00003
Feruloyltyramine
2 spectra
C18H19NO4
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
313.13141
LC-ESI-ITTOF; MS2; [M+H]+
MSJ00002
LC-ESI-ITTOF; MS; Positive
MSJ00001
Feselol
5 spectra
C24H30O4
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
382.50430
LC-ESI-QQQ; MS2; Frag=135.0V CID@10.0; [M+H]+
NGA01947
LC-ESI-QQQ; MS2; Frag=135.0V CID@15.0; [M+H]+
NGA01946
LC-ESI-QQQ; MS2; Frag=135.0V CID@25.0; [M+H]+
NGA01945
LC-ESI-QQQ; MS2; Frag=135.0V CID@5.0; [M+H]+
NGA01948
LC-ESI-QQQ; MS; [M+H]+
CB000264
Fexofenadine
12 spectra
C32H39NO4
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
501.28790
LC-ESI-QFT; MS2; CE: 15; R=35000; [M+H]+
EQ301901
LC-ESI-QFT; MS2; CE: 15; R=35000; [M-H]-
EQ301951
LC-ESI-QFT; MS2; CE: 30; R=35000; [M+H]+
EQ301902
LC-ESI-QFT; MS2; CE: 30; R=35000; [M-H]-
EQ301952
LC-ESI-QFT; MS2; CE: 45; R=35000; [M+H]+
EQ301903
LC-ESI-QFT; MS2; CE: 45; R=35000; [M-H]-
EQ301953
LC-ESI-QFT; MS2; CE: 60; R=35000; [M+H]+
EQ301904
LC-ESI-QFT; MS2; CE: 60; R=35000; [M-H]-
EQ301954
LC-ESI-QFT; MS2; CE: 75; R=35000; [M+H]+
EQ301905
LC-ESI-QFT; MS2; CE: 75; R=35000; [M-H]-
EQ301955
LC-ESI-QFT; MS2; CE: 90; R=35000; [M+H]+
EQ301906
LC-ESI-QFT; MS2; CE: 90; R=35000; [M-H]-
EQ301956
FFA_n_189.0167_20.1
1 spectrum
C8H5F3O2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
190.02420
LC-ESI-QFT; MS2; CE: 85%; R=17500; [M-H]-
ET405801
FILIFOLIDE A
1 spectrum
C10H14O2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
166.09938
EI-B; MS
JP006309
FILIFOLONE
1 spectrum
C10H14O
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
150.10448
EI-B; MS
JP006311
Finasteride
16 spectra
C23H36N2O2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
372.27771
LC-ESI-ITFT; MS2; CE: 35; R=15000; [M+H]+
UF411503
LC-ESI-ITFT; MS2; CE: 55; R=15000; [M+H]+
UF411501
LC-ESI-ITFT; MS2; CE: 55; R=15000; [M+H]+
UF411504
LC-ESI-ITFT; MS2; CE: 80; R=15000; [M+H]+
UF411502
LC-ESI-QFT; MS2; CE: 15; R=17500; [M+H]+
LU054101
LC-ESI-QFT; MS2; CE: 30; R=17500; [M+H]+
LU054102
LC-ESI-QFT; MS2; CE: 45; R=17500; [M+H]+
LU054103
LC-ESI-QFT; MS2; CE: 60; R=17500; [M+H]+
LU054104
LC-ESI-QFT; MS2; CE: 75; R=17500; [M+H]+
LU054105
LC-ESI-QFT; MS2; CE: 90; R=17500; [M+H]+
LU054106
LC-ESI-QTOF; MS2; CE: 10 eV; R=35000; [M+H]+
AU270201
LC-ESI-QTOF; MS2; CE: 20 eV; R=35000; [M+H]+
AU270202
LC-ESI-QTOF; MS2; CE: 30 eV; R=35000; [M+H]+
AU270203
LC-ESI-QTOF; MS2; CE: 40 eV; R=35000; [M+H]+
AU270204
LC-ESI-QTOF; MS2; CE: 50 eV; R=35000; [M+H]+
AU270205
LC-ESI-QTOF; MS2; CE: Ramp 23.1-34.6 eV; R=35000; [M+H]+
AU270206
Fipexide
12 spectra
C20H21ClN2O4
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
388.11899
LC-ESI-Q; MS; POS; 15 V
WA002733
LC-ESI-Q; MS; POS; 30 V
WA002732
LC-ESI-Q; MS; POS; 45 V
WA002731
LC-ESI-Q; MS; POS; 60 V
WA002730
LC-ESI-Q; MS; POS; 75 V
WA002729
LC-ESI-Q; MS; POS; 90 V
WA002728
LC-ESI-QFT; MS2; CE: 15; R=17500; [M+H]+
LU132401
LC-ESI-QFT; MS2; CE: 30; R=17500; [M+H]+
LU132402
LC-ESI-QFT; MS2; CE: 45; R=17500; [M+H]+
LU132403
LC-ESI-QFT; MS2; CE: 60; R=17500; [M+H]+
LU132404
LC-ESI-QFT; MS2; CE: 75; R=17500; [M+H]+
LU132405
LC-ESI-QFT; MS2; CE: 90; R=17500; [M+H]+
LU132406
Fipronil
28 spectra
C12H4Cl2F6N4OS
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
435.93869
LC-ESI-ITFT; MS2; CE: 15%; R=15000; [M+H]+
EA266608
LC-ESI-ITFT; MS2; CE: 15%; R=15000; [M-H]-
EA266658
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M+H]+
EA266602
LC-ESI-ITFT; MS2; CE: 15%; R=7500; [M-H]-
EA266652
LC-ESI-ITFT; MS2; CE: 30%; R=15000; [M+H]+
EA266609
LC-ESI-ITFT; MS2; CE: 30%; R=15000; [M-H]-
EA266659
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M+H]+
EA266603
LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M-H]-
EA266653
LC-ESI-ITFT; MS2; CE: 35%; R=30000; [M+H]+
EA266614
LC-ESI-ITFT; MS2; CE: 35%; R=30000; [M-H]-
EA266664
LC-ESI-ITFT; MS2; CE: 35%; R=7500; [M+H]+
EA266601
LC-ESI-ITFT; MS2; CE: 35%; R=7500; [M-H]-
EA266651
LC-ESI-ITFT; MS2; CE: 45%; R=15000; [M+H]+
EA266610
LC-ESI-ITFT; MS2; CE: 45%; R=15000; [M-H]-
EA266660
LC-ESI-ITFT; MS2; CE: 45%; R=7500; [M+H]+
EA266604
LC-ESI-ITFT; MS2; CE: 45%; R=7500; [M-H]-
EA266654
LC-ESI-ITFT; MS2; CE: 60%; R=15000; [M+H]+
EA266611
LC-ESI-ITFT; MS2; CE: 60%; R=15000; [M-H]-
EA266661
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M+H]+
EA266605
LC-ESI-ITFT; MS2; CE: 60%; R=7500; [M-H]-
EA266655
LC-ESI-ITFT; MS2; CE: 75%; R=15000; [M+H]+
EA266612
LC-ESI-ITFT; MS2; CE: 75%; R=15000; [M-H]-
EA266662
LC-ESI-ITFT; MS2; CE: 75%; R=7500; [M+H]+
EA266606
LC-ESI-ITFT; MS2; CE: 75%; R=7500; [M-H]-
EA266656
LC-ESI-ITFT; MS2; CE: 90%; R=30000; [M+H]+
EA266613
LC-ESI-ITFT; MS2; CE: 90%; R=30000; [M-H]-
EA266663
LC-ESI-ITFT; MS2; CE: 90%; R=7500; [M+H]+
EA266607
LC-ESI-ITFT; MS2; CE: 90%; R=7500; [M-H]-
EA266657
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