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1,466 Hit.
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Name
Formula / Structure
ExactMass
ID
Oleanane -4H, + 2O
1 spectrum
C30H48O2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
440.71201
LC-ESI-QTOF; MS2
PR310658
Oleanane -4H, + 2O, 1COOH, O-HexA, HexA
1 spectrum
C42H62O16
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
822.94202
LC-ESI-QTOF; MS2
PR308908
Oleanane -4H, +2O, 1COOH, O-HexA, HexA
1 spectrum
C42H62O16
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
822.94202
LC-ESI-QTOF; MS2
PR310661
Oleandomycin
7 spectra
C35H61NO12
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
687.41937
LC-ESI-IT; MS2; m/z: 688; [M+H]+
KO009136
LC-ESI-IT; MS3; m/z: 688/544; [M+H]+
KO009137
LC-ESI-QQ; MS2; CE:10 V; [M+H]+
KO003661
LC-ESI-QQ; MS2; CE:20 V; [M+H]+
KO003662
LC-ESI-QQ; MS2; CE:30 V; [M+H]+
KO003663
LC-ESI-QQ; MS2; CE:40 V; [M+H]+
KO003664
LC-ESI-QQ; MS2; CE:50 V; [M+H]+
KO003665
Oleandrin
9 spectra
C32H48O9
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
576.32977
LC-ESI-ITFT; MS2; CE: 15%; R=15000; [M+H]+
NA002307
LC-ESI-ITFT; MS2; CE: 25%; R=15000; [M+H]+
NA002308
LC-ESI-ITFT; MS2; CE: 35%; R=15000; [M+H]+
NA002702
LC-ESI-ITFT; MS2; CE: 45%; R=15000; [M+H]+
NA002703
LC-ESI-Q; MS; NEG; 30 V
WA002671
LC-ESI-Q; MS; POS; 15 V
WA002670
LC-ESI-Q; MS; POS; 30 V
WA002669
LC-ESI-Q; MS; POS; 45 V
WA002668
LC-ESI-Q; MS; POS; 60 V, 90 V
WA002667
Oleanolic acid
12 spectra
C30H48O3
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
456.36035
LC-APCI-QTOF; MS; NEGATIVE
BML81848
LC-APCI-QTOF; MS; POSITIVE
BML81847
LC-ESI-QTOF; MS2; [M-H]-; CE: 10eV
FIO01059
LC-ESI-QTOF; MS2; [M-H]-; CE: 20eV
FIO01060
LC-ESI-QTOF; MS2; [M-H]-; CE: 30eV
FIO01061
LC-ESI-QTOF; MS2; [M-H]-; CE: 40eV
FIO01062
LC-ESI-QTOF; MS2; [M-H]-; CE: 50eV
FIO01063
LC-ESI-QTOF; MS2; CE 10 ev; [M-H]-
BML00591
LC-ESI-QTOF; MS2; CE 20 ev; [M-H]-
BML00596
LC-ESI-QTOF; MS2; CE 40 ev; [M-H]-
BML00601
LC-ESI-QTOF; MS; NEGATIVE
BML81846
LC-ESI-QTOF; MS; POSITIVE
BML81845
Oleanolic acid base + O-HexA-Hex
1 spectrum
C42H66O14
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
794.97601
LC-ESI-QTOF; MS2
PR308912
Oleic acid
10 spectra
C18H34O2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
282.25589
FAB-EBEB; MS2; m/z: 281.25; [M-H]-
CA000168
LC-ESI-QTOF; MS
BS003991
LC-ESI-QTOF; MS2; CE:10 eV; [M-H]-
BS003988
LC-ESI-QTOF; MS2; CE:20 eV; [M-H]-
BS003989
LC-ESI-QTOF; MS2; CE:30 eV; [M-H]-
BS003990
LC-ESI-QTOF; MS; CE:10 eV; [M-H]-
BS003992
OLEIC ACID
1 spectrum
C18H34O2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
282.25589
EI-B; MS
JP003087
Oleic acid
10 spectra
C18H34O2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
282.25589
GC-EI-TOF; MS; 1 TMS; BP:73
PR010209
LC-ESI-IT; MS2; m/z: 281.3; [M-H]-
MT000029
LC-ESI-QTOF; MS2; CE: 10; R=; [M-H]-
RP029011
LC-ESI-QTOF; MS2; CE: 20; R=; [M-H]-
RP029012
OLEIC ACID TRIMETHYLSILYL ESTER
1 spectrum
C21H42O2Si
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
354.29541
EI-B; MS
JP000582
Oleonolic acid
1 spectrum
C30H48O3
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
456.36035
LC-ESI-ITTOF; MS; [M-H]-
TY000153
Oleoyl Ethanolamide
3 spectra
C20H39NO2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
325.29807
LC-ESI-QTOF; MS2; CE: 10; R=; [M+H]+
RP003101
LC-ESI-QTOF; MS2; CE: 20; R=; [M+H]+
RP003102
LC-ESI-QTOF; MS2; CE: 40; R=; [M+H]+
RP003103
Oleoyl-L-Carnitine
3 spectra
C25H47NO4
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
425.35049
LC-ESI-QTOF; MS2; CE: 10; R=; [M+H]+
RP025101
LC-ESI-QTOF; MS2; CE: 20; R=; [M+H]+
RP025102
LC-ESI-QTOF; MS2; CE: 40; R=; [M+H]+
RP025103
Oleuropein
1 spectrum
C25H32O13
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
540.52600
LC-ESI-QQQ; MS; [M+H]+
CB000432
OLEYL ACETATE
1 spectrum
C20H38O2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
310.28717
EI-B; MS
JP002528
OLEYL AMIDE
2 spectra
C18H35NO
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
281.27185
EI-B; MS
JP003588
EI-B; MS
JP008351
Oleyl sarcosine
12 spectra
C21H39NO3
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
353.29300
LC-ESI-QFT; MS2; CE: 15; R=17500; [M+H]+
LU033601
LC-ESI-QFT; MS2; CE: 15; R=17500; [M-H]-
LU033651
LC-ESI-QFT; MS2; CE: 30; R=17500; [M+H]+
LU033602
LC-ESI-QFT; MS2; CE: 30; R=17500; [M-H]-
LU033652
LC-ESI-QFT; MS2; CE: 45; R=17500; [M+H]+
LU033603
LC-ESI-QFT; MS2; CE: 45; R=17500; [M-H]-
LU033653
LC-ESI-QFT; MS2; CE: 60; R=17500; [M+H]+
LU033604
LC-ESI-QFT; MS2; CE: 60; R=17500; [M-H]-
LU033654
LC-ESI-QFT; MS2; CE: 75; R=17500; [M+H]+
LU033605
LC-ESI-QFT; MS2; CE: 75; R=17500; [M-H]-
LU033655
LC-ESI-QFT; MS2; CE: 90; R=17500; [M+H]+
LU033606
LC-ESI-QFT; MS2; CE: 90; R=17500; [M-H]-
LU033656
OLIGOMYCIN-A
1 spectrum
C45H74O11
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
790.52313
FD-B; MS
JP000144
Olitoriside
8 spectra
C35H52O14
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
696.79633
LC-ESI-QQQ; MS2; Frag=135.0V CID@10.0; [M+H]+
NGA03191
LC-ESI-QQQ; MS2; Frag=135.0V CID@10.0; [M+HCOO]-
NGA05076
LC-ESI-QQQ; MS2; Frag=135.0V CID@15.0; [M+H]+
NGA03190
LC-ESI-QQQ; MS2; Frag=135.0V CID@15.0; [M+HCOO]-
NGA05077
LC-ESI-QQQ; MS2; Frag=135.0V CID@25.0; [M+H]+
NGA03189
LC-ESI-QQQ; MS2; Frag=135.0V CID@25.0; [M+HCOO]-
NGA05078
LC-ESI-QQQ; MS2; Frag=135.0V CID@5.0; [M+H]+
NGA03192
LC-ESI-QQQ; MS2; Frag=135.0V CID@5.0; [M+HCOO]-
NGA05075
Olivetol
5 spectra
C11H16O2
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
180.11501
LC-ESI-QFT; MS2; CE: 15; R=17500; [M-H]-
LU104951
LC-ESI-QFT; MS2; CE: 30; R=17500; [M-H]-
LU104952
LC-ESI-QFT; MS2; CE: 45; R=17500; [M-H]-
LU104953
LC-ESI-QFT; MS2; CE: 60; R=17500; [M-H]-
LU104954
LC-ESI-QFT; MS2; CE: 75; R=17500; [M-H]-
LU104955
OLMESARTAN MEDOXOMIL
1 spectrum
C29H30N6O6
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
558.22266
ESI-QTOF; MS2; CE 25eV; [M-H]-
UPA00016
Olopatadine
23 spectra
C21H23NO3
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
337.16779
LC-ESI-QFT; MS2; CE: 15; R=35000; [M+H]+
EQ332301
LC-ESI-QFT; MS2; CE: 15; R=35000; [M-H]-
EQ332351
LC-ESI-QFT; MS2; CE: 30; R=35000; [M+H]+
EQ332302
LC-ESI-QFT; MS2; CE: 30; R=35000; [M-H]-
EQ332352
LC-ESI-QFT; MS2; CE: 45; R=35000; [M+H]+
EQ332303
LC-ESI-QFT; MS2; CE: 45; R=35000; [M-H]-
EQ332353
LC-ESI-QFT; MS2; CE: 60; R=35000; [M+H]+
EQ332304
LC-ESI-QFT; MS2; CE: 60; R=35000; [M-H]-
EQ332354
LC-ESI-QFT; MS2; CE: 75; R=35000; [M+H]+
EQ332305
LC-ESI-QFT; MS2; CE: 75; R=35000; [M-H]-
EQ332355
LC-ESI-QFT; MS2; CE: 90; R=35000; [M+H]+
EQ332306
LC-ESI-QFT; MS2; CE: 90; R=35000; [M-H]-
EQ332356
LC-ESI-QTOF; MS2; CE: 10 eV; R=35000; [M+H]+
AU221001
LC-ESI-QTOF; MS2; CE: 20 eV; R=35000; [M+H]+
AU221002
LC-ESI-QTOF; MS2; CE: 20 eV; R=35000; [M+Na]+
AU221031
LC-ESI-QTOF; MS2; CE: 30 eV; R=35000; [M+H]+
AU221003
LC-ESI-QTOF; MS2; CE: 40 eV; R=35000; [M+H]+
AU221004
LC-ESI-QTOF; MS2; CE: 50 eV; R=35000; [M+H]+
AU221005
LC-ESI-QTOF; MS2; HILIC; CE: 10 eV; R=35000; [M+H]+
AU221007
LC-ESI-QTOF; MS2; HILIC; CE: 20 eV; R=35000; [M+H]+
AU221008
LC-ESI-QTOF; MS2; HILIC; CE: 30 eV; R=35000; [M+H]+
AU221009
LC-ESI-QTOF; MS2; HILIC; CE: 40 eV; R=35000; [M+H]+
AU221010
LC-ESI-QTOF; MS2; HILIC; CE: 50 eV; R=35000; [M+H]+
AU221011
Omeprazole
13 spectra
C17H19N3O3S
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
345.11472
LC-ESI-Q; MS; NEG; 30 V
WA002657
LC-ESI-Q; MS; POS; 15 V
WA002656
LC-ESI-Q; MS; POS; 30 V
WA002655
LC-ESI-Q; MS; POS; 45 V
WA002654
LC-ESI-Q; MS; POS; 60 V
WA002653
LC-ESI-Q; MS; POS; 75 V, 90 V
WA002652
LC-ESI-QFT; MS2; CE: 35 NCE; R=35000; [M+H]+
SM833401
LC-ESI-QFT; MS2; CE: 35 NCE; R=35000; [M-H]-
SM833453
LC-ESI-QTOF; MS2; CE: 10 eV; R=35000; [M+H]+
AU111301
LC-ESI-QTOF; MS2; CE: 20 eV; R=35000; [M+H]+
AU111302
LC-ESI-QTOF; MS2; CE: 30 eV; R=35000; [M+H]+
AU111303
LC-ESI-QTOF; MS2; CE: 40 eV; R=35000; [M+H]+
AU111304
LC-ESI-QTOF; MS2; CE: 50 eV; R=35000; [M+H]+
AU111305
Omethoate
13 spectra
C5H12NO4PS
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
213.02246
LC-ESI-QTOF; MS2; CE: 10 eV; R=35000; [M+H]+
AU302701
LC-ESI-QTOF; MS2; CE: 10 eV; R=35000; [M+Na]+
AU302730
LC-ESI-QTOF; MS2; CE: 20 eV; R=35000; [M+H]+
AU302702
LC-ESI-QTOF; MS2; CE: 20 eV; R=35000; [M+Na]+
AU302731
LC-ESI-QTOF; MS2; CE: 30 eV; R=35000; [M+H]+
AU302703
LC-ESI-QTOF; MS2; CE: 40 eV; R=35000; [M+H]+
AU302704
LC-ESI-QTOF; MS2; CE: 50 eV; R=35000; [M+H]+
AU302705
LC-ESI-QTOF; MS2; CE: Ramp 18.5-27.8 eV; R=35000; [M+H]+
AU302706
LC-ESI-QTOF; MS2; HILIC; CE: 10 eV; R=35000; [M+H]+
AU302707
LC-ESI-QTOF; MS2; HILIC; CE: 20 eV; R=35000; [M+H]+
AU302708
LC-ESI-QTOF; MS2; HILIC; CE: 30 eV; R=35000; [M+H]+
AU302709
LC-ESI-QTOF; MS2; HILIC; CE: 40 eV; R=35000; [M+H]+
AU302710
LC-ESI-QTOF; MS2; HILIC; CE: 50 eV; R=35000; [M+H]+
AU302711
OMT, L-Lobamine Sulfone, L-Methionine S-dioxide, M...
9 spectra
C5H11NO4S
Generated by the Chemistry Development Kit (http://github.com/cdk)
\n
181.21100
LC-ESI-QQ; MS2
PS028201
LC-ESI-QQ; MS2
PS028202
LC-ESI-QQ; MS2
PS028203
LC-ESI-QQ; MS2
PS028204
LC-ESI-QQ; MS2
PS028205
LC-ESI-QQ; MS2
PS028206
LC-ESI-QQ; MS2
PS028207
LC-ESI-QQ; MS2
PS028208
LC-ESI-QQ; MS2
PS028209
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