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8,299 Hit.
( 6,200 - 6,320 Displayed )
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Name
Formula / Structure
ExactMass
ID
Coumarin base + 1O, 1MeO, O-Hex
1 spectrum
C16H18O9
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
354.31100
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR309350
Coumaroyl + C6H9O8 (isomer of 843, 844, 845)
1 spectrum
C15H16O10
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
356.28299
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR309203
Coumaroyl + C6H9O8 (isomer of 843, 844, 846)
1 spectrum
C15H16O10
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
356.28299
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR309201
Coumaroyl + C6H9O8 (isomer of 843, 845, 846)
1 spectrum
C15H16O10
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
356.28299
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR309202
Coumaroyl + C6H9O8 (isomer of 844, 845, 846)
1 spectrum
C15H16O10
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
356.28299
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR309200
Coumaroyl agmatine (isomer of 1296)
1 spectrum
C14H20N4O2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
276.34000
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR311080
Coumaroyl agmatine (isomer of 1297)
1 spectrum
C14H20N4O2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
276.34000
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR311079
Coumaroyl Hexoside (isomer of 690, 691)
1 spectrum
C15H18O8
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
326.30099
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR309359
Coumaroyl Hexoside (isomer of 690, 692)
1 spectrum
C15H18O8
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
326.30099
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR309358
Coumaroyl Hexoside (isomer of 691, 692)
1 spectrum
C15H18O8
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
326.30099
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR309357
Coumaroyl putrescin
1 spectrum
C13H18N2O2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
234.29900
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR311078
Coumaroyl quinic acid (isomer of 758, 759)
1 spectrum
C16H18O8
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
338.31201
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR309014
Coumaroyl quinic acid (isomer of 758, 760)
1 spectrum
C16H18O8
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
338.31201
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR309013
Coumaroyl quinic acid (isomer of 759, 760)
1 spectrum
C16H18O8
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
338.31201
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR309361
Coumaroyl tyramine
1 spectrum
C17H17NO3
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
283.32700
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR311081
Coumatetralyl
37 spectra
C19H16O3
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
292.10995
LC-ESI-Q; MS; NEG; 30 V
MSBNK-Waters-WA002777
LC-ESI-Q; MS; POS; 15 V
MSBNK-Waters-WA002783
LC-ESI-Q; MS; POS; 30 V
MSBNK-Waters-WA002782
LC-ESI-Q; MS; POS; 45 V
MSBNK-Waters-WA002781
LC-ESI-Q; MS; POS; 60 V
MSBNK-Waters-WA002780
LC-ESI-Q; MS; POS; 75 V
MSBNK-Waters-WA002779
LC-ESI-Q; MS; POS; 90 V
MSBNK-Waters-WA002778
LC-ESI-QFT; MS2; CE: 120%; R=17500; [M+H]+
MSBNK-Eawag-EQ01094507
LC-ESI-QFT; MS2; CE: 120%; R=17500; [M-H]-
MSBNK-Eawag-EQ01094557
LC-ESI-QFT; MS2; CE: 15%; R=17500; [M+H]+
MSBNK-Eawag-EQ01094501
LC-ESI-QFT; MS2; CE: 15%; R=17500; [M-H]-
MSBNK-Eawag-EQ01094551
LC-ESI-QFT; MS2; CE: 150%; R=17500; [M+H]+
MSBNK-Eawag-EQ01094508
LC-ESI-QFT; MS2; CE: 150%; R=17500; [M-H]-
MSBNK-Eawag-EQ01094558
LC-ESI-QFT; MS2; CE: 15; R=17500; [M+H]+
MSBNK-LCSB-LU071001
LC-ESI-QFT; MS2; CE: 15; R=17500; [M-H]-
MSBNK-LCSB-LU071051
LC-ESI-QFT; MS2; CE: 180%; R=17500; [M+H]+
MSBNK-Eawag-EQ01094509
LC-ESI-QFT; MS2; CE: 180%; R=17500; [M-H]-
MSBNK-Eawag-EQ01094559
LC-ESI-QFT; MS2; CE: 30%; R=17500; [M+H]+
MSBNK-Eawag-EQ01094502
LC-ESI-QFT; MS2; CE: 30%; R=17500; [M-H]-
MSBNK-Eawag-EQ01094552
LC-ESI-QFT; MS2; CE: 30; R=17500; [M+H]+
MSBNK-LCSB-LU071002
LC-ESI-QFT; MS2; CE: 30; R=17500; [M-H]-
MSBNK-LCSB-LU071052
LC-ESI-QFT; MS2; CE: 45%; R=17500; [M+H]+
MSBNK-Eawag-EQ01094503
LC-ESI-QFT; MS2; CE: 45%; R=17500; [M-H]-
MSBNK-Eawag-EQ01094553
LC-ESI-QFT; MS2; CE: 45; R=17500; [M+H]+
MSBNK-LCSB-LU071003
LC-ESI-QFT; MS2; CE: 45; R=17500; [M-H]-
MSBNK-LCSB-LU071053
LC-ESI-QFT; MS2; CE: 60%; R=17500; [M+H]+
MSBNK-Eawag-EQ01094504
LC-ESI-QFT; MS2; CE: 60%; R=17500; [M-H]-
MSBNK-Eawag-EQ01094554
LC-ESI-QFT; MS2; CE: 60; R=17500; [M+H]+
MSBNK-LCSB-LU071004
LC-ESI-QFT; MS2; CE: 60; R=17500; [M-H]-
MSBNK-LCSB-LU071054
LC-ESI-QFT; MS2; CE: 75%; R=17500; [M+H]+
MSBNK-Eawag-EQ01094505
LC-ESI-QFT; MS2; CE: 75%; R=17500; [M-H]-
MSBNK-Eawag-EQ01094555
LC-ESI-QFT; MS2; CE: 75; R=17500; [M+H]+
MSBNK-LCSB-LU071005
LC-ESI-QFT; MS2; CE: 75; R=17500; [M-H]-
MSBNK-LCSB-LU071055
LC-ESI-QFT; MS2; CE: 90%; R=17500; [M+H]+
MSBNK-Eawag-EQ01094506
LC-ESI-QFT; MS2; CE: 90%; R=17500; [M-H]-
MSBNK-Eawag-EQ01094556
LC-ESI-QFT; MS2; CE: 90; R=17500; [M+H]+
MSBNK-LCSB-LU071006
LC-ESI-QFT; MS2; CE: 90; R=17500; [M-H]-
MSBNK-LCSB-LU071056
Coumestan base + 2O
1 spectrum
C15H8O5
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
268.22400
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR311075
Coumestan base + 2O, O-Hex
2 spectra
C21H18O10
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
430.36499
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR309351
LC-ESI-QTOF; MS2
MSBNK-RIKEN-PR311076
Coumestrol
6 spectra
C15H8O5
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
268.03720
LC-ESI-QTOF; MS2; CE:10 eV; [M-H]-
MSBNK-BS-BS003252
LC-ESI-QTOF; MS2; CE:20 eV; [M-H]-
MSBNK-BS-BS003251
LC-ESI-QTOF; MS2; CE:30 eV; [M-H]-
MSBNK-BS-BS003253
LC-ESI-QTOF; MS2; CE:40 eV; [M-H]-
MSBNK-BS-BS003254
LC-ESI-QTOF; MS2; CE:50 eV; [M-H]-
MSBNK-BS-BS003256
LC-ESI-QTOF; MS; CE:10 eV; [M-H]-
MSBNK-BS-BS003255
Coumoxystrobin
9 spectra
C26H28O6
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
436.18860
LC-ESI-QFT; MS2; CE: 120%; R=17500; [M+H]+
MSBNK-Eawag-EQ01121916
LC-ESI-QFT; MS2; CE: 15%; R=17500; [M+H]+
MSBNK-Eawag-EQ01121910
LC-ESI-QFT; MS2; CE: 150%; R=17500; [M+H]+
MSBNK-Eawag-EQ01121917
LC-ESI-QFT; MS2; CE: 180%; R=17500; [M+H]+
MSBNK-Eawag-EQ01121918
LC-ESI-QFT; MS2; CE: 30%; R=17500; [M+H]+
MSBNK-Eawag-EQ01121911
LC-ESI-QFT; MS2; CE: 45%; R=17500; [M+H]+
MSBNK-Eawag-EQ01121912
LC-ESI-QFT; MS2; CE: 60%; R=17500; [M+H]+
MSBNK-Eawag-EQ01121913
LC-ESI-QFT; MS2; CE: 75%; R=17500; [M+H]+
MSBNK-Eawag-EQ01121914
LC-ESI-QFT; MS2; CE: 90%; R=17500; [M+H]+
MSBNK-Eawag-EQ01121915
CP-100829
3 spectra
C14H7Cl2FN2O3S
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
371.95386
ESI-QTOF; MS2; CE: 10; [M-H]-
MSBNK-EPA-ENTACT_AGILENT001942
ESI-QTOF; MS2; CE: 20; [M-H]-
MSBNK-EPA-ENTACT_AGILENT001941
ESI-QTOF; MS2; CE: 40; [M-H]-
MSBNK-EPA-ENTACT_AGILENT001940
CP-114271
18 spectra
C17H19F3N2O4S
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
404.10178
ESI-QTOF; MS2; CE: 10; [M+H]+
MSBNK-EPA-ENTACT_AGILENT001779
ESI-QTOF; MS2; CE: 10; [M-H]-
MSBNK-EPA-ENTACT_AGILENT001778
ESI-QTOF; MS2; CE: 20; [M+H]+
MSBNK-EPA-ENTACT_AGILENT001780
ESI-QTOF; MS2; CE: 20; [M-H]-
MSBNK-EPA-ENTACT_AGILENT001777
ESI-QTOF; MS2; CE: 40; [M+H]+
MSBNK-EPA-ENTACT_AGILENT001776
ESI-QTOF; MS2; CE: 40; [M-H]-
MSBNK-EPA-ENTACT_AGILENT001781
LC-ESI-QFT; MS2; CE: 15; R=17500; [M+H]+
MSBNK-LCSB-LU026501
LC-ESI-QFT; MS2; CE: 15; R=17500; [M-H]-
MSBNK-LCSB-LU026551
LC-ESI-QFT; MS2; CE: 30; R=17500; [M+H]+
MSBNK-LCSB-LU026502
LC-ESI-QFT; MS2; CE: 30; R=17500; [M-H]-
MSBNK-LCSB-LU026552
LC-ESI-QFT; MS2; CE: 45; R=17500; [M+H]+
MSBNK-LCSB-LU026503
LC-ESI-QFT; MS2; CE: 45; R=17500; [M-H]-
MSBNK-LCSB-LU026553
LC-ESI-QFT; MS2; CE: 60; R=17500; [M+H]+
MSBNK-LCSB-LU026504
LC-ESI-QFT; MS2; CE: 60; R=17500; [M-H]-
MSBNK-LCSB-LU026554
LC-ESI-QFT; MS2; CE: 75; R=17500; [M+H]+
MSBNK-LCSB-LU026505
LC-ESI-QFT; MS2; CE: 75; R=17500; [M-H]-
MSBNK-LCSB-LU026555
LC-ESI-QFT; MS2; CE: 90; R=17500; [M+H]+
MSBNK-LCSB-LU026506
LC-ESI-QFT; MS2; CE: 90; R=17500; [M-H]-
MSBNK-LCSB-LU026556
CP-122721
9 spectra
C20H23F3N2O2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
380.17117
ESI-QTOF; MS2; CE: 10; [M+H]+
MSBNK-EPA-ENTACT_AGILENT000969
ESI-QTOF; MS2; CE: 20; [M+H]+
MSBNK-EPA-ENTACT_AGILENT000967
ESI-QTOF; MS2; CE: 40; [M+H]+
MSBNK-EPA-ENTACT_AGILENT000968
LC-ESI-QFT; MS2; CE: 15; R=17500; [M+H]+
MSBNK-LCSB-LU044301
LC-ESI-QFT; MS2; CE: 30; R=17500; [M+H]+
MSBNK-LCSB-LU044302
LC-ESI-QFT; MS2; CE: 45; R=17500; [M+H]+
MSBNK-LCSB-LU044303
LC-ESI-QFT; MS2; CE: 60; R=17500; [M+H]+
MSBNK-LCSB-LU044304
LC-ESI-QFT; MS2; CE: 75; R=17500; [M+H]+
MSBNK-LCSB-LU044305
LC-ESI-QFT; MS2; CE: 90; R=17500; [M+H]+
MSBNK-LCSB-LU044306
CP-401387
12 spectra
C23H29N3O2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
379.22601
LC-ESI-QFT; MS2; CE: 15; R=17500; [M+H]+
MSBNK-LCSB-LU073301
LC-ESI-QFT; MS2; CE: 15; R=17500; [M-H]-
MSBNK-LCSB-LU073351
LC-ESI-QFT; MS2; CE: 30; R=17500; [M+H]+
MSBNK-LCSB-LU073302
LC-ESI-QFT; MS2; CE: 30; R=17500; [M-H]-
MSBNK-LCSB-LU073352
LC-ESI-QFT; MS2; CE: 45; R=17500; [M+H]+
MSBNK-LCSB-LU073303
LC-ESI-QFT; MS2; CE: 45; R=17500; [M-H]-
MSBNK-LCSB-LU073353
LC-ESI-QFT; MS2; CE: 60; R=17500; [M+H]+
MSBNK-LCSB-LU073304
LC-ESI-QFT; MS2; CE: 60; R=17500; [M-H]-
MSBNK-LCSB-LU073354
LC-ESI-QFT; MS2; CE: 75; R=17500; [M+H]+
MSBNK-LCSB-LU073305
LC-ESI-QFT; MS2; CE: 75; R=17500; [M-H]-
MSBNK-LCSB-LU073355
LC-ESI-QFT; MS2; CE: 90; R=17500; [M+H]+
MSBNK-LCSB-LU073306
LC-ESI-QFT; MS2; CE: 90; R=17500; [M-H]-
MSBNK-LCSB-LU073356
CP-409092
9 spectra
C17H19N3O2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
297.14774
ESI-QTOF; MS2; CE: 10; [M+H]+
MSBNK-EPA-ENTACT_AGILENT000963
ESI-QTOF; MS2; CE: 20; [M+H]+
MSBNK-EPA-ENTACT_AGILENT000961
ESI-QTOF; MS2; CE: 40; [M+H]+
MSBNK-EPA-ENTACT_AGILENT000962
LC-ESI-QFT; MS2; CE: 15; R=17500; [M-H]-
MSBNK-LCSB-LU053851
LC-ESI-QFT; MS2; CE: 30; R=17500; [M-H]-
MSBNK-LCSB-LU053852
LC-ESI-QFT; MS2; CE: 45; R=17500; [M-H]-
MSBNK-LCSB-LU053853
LC-ESI-QFT; MS2; CE: 60; R=17500; [M-H]-
MSBNK-LCSB-LU053854
LC-ESI-QFT; MS2; CE: 75; R=17500; [M-H]-
MSBNK-LCSB-LU053855
LC-ESI-QFT; MS2; CE: 90; R=17500; [M-H]-
MSBNK-LCSB-LU053856
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