Acetaminophen |
1 g/kg |
6 hours |
mice; C57Bl/6 |
in vivo |
GSH level measurement |
increase |
Positive |
p < 0.05 |
1 |
Acetaminophen |
1 g/kg |
12 hours |
mice; C57Bl/6 |
in vivo |
GSH level measurement |
increase |
Positive |
p < 0.05 |
1 |
Acetaminophen |
1 g/kg |
24 hours |
mice; C57Bl/6 |
in vivo |
GSH level measurement |
increase |
Positive |
p < 0.05 |
1 |
Oligomycin |
8 nM |
|
bovine |
heart mitochondria |
Measurement of complex V activity |
decrease |
Positive |
IC50 |
3 |
aurovertin B |
1.5 μM |
|
bovine |
heart mitochondria |
Measurement of complex V activity |
decrease |
Positive |
IC50 |
3 |
Amiodarone |
50 μM |
|
bovine |
heart mitochondria |
Measurement of complex I activity |
decrease |
Positive |
p < 0.05 |
3 |
Amiodarone |
50 μM |
|
bovine |
heart mitochondria |
Measurement of complex II + III activity |
decrease |
Positive |
p < 0.001 |
3 |
Amiodarone |
50 μM |
|
bovine |
heart mitochondria |
Measurement of complex II + III activity |
decrease |
Positive |
p < 0.001 |
3 |
Amiodarone |
50 μM |
|
bovine |
heart mitochondria |
Measurement of complex IV activity |
decrease |
Positive |
p < 0.05 |
3 |
Amiodarone |
50 μM |
|
bovine |
heart mitochondria |
Measurement of complex V activity |
decrease |
Positive |
p < 0.001 |
3 |
Chlorpromazine |
50 μM |
|
bovine |
heart mitochondria |
Measurement of complex II + III activity |
decrease |
Positive |
p < 0.001 |
3 |
Chlorpromazine |
50 μM |
|
bovine |
heart mitochondria |
Measurement of complex II + III activity |
decrease |
Positive |
p < 0.001 |
3 |
Chlorpromazine |
50 μM |
|
bovine |
heart mitochondria |
Measurement of complex V activity |
decrease |
Positive |
p < 0.001 |
3 |
Diclofenac |
50 μM |
|
bovine |
heart mitochondria |
Measurement of complex V activity |
decrease |
Positive |
p < 0.01 |
3 |
gefitinib |
50 μM |
|
bovine |
heart mitochondria |
Measurement of complex IV activity |
decrease |
Positive |
p < 0.05 |
3 |
gefitinib |
50 μM |
|
bovine |
heart mitochondria |
Measurement of complex V activity |
decrease |
Positive |
p < 0.001 |
3 |
Nefazodone |
50 μM |
|
bovine |
heart mitochondria |
Measurement of complex I activity |
decrease |
Positive |
p < 0.001 |
3 |
Nefazodone |
50 μM |
|
bovine |
heart mitochondria |
Measurement of complex II + III activity |
decrease |
Positive |
p < 0.01 |
3 |
Nefazodone |
50 μM |
|
bovine |
heart mitochondria |
Measurement of complex II + III activity |
decrease |
Positive |
p < 0.01 |
3 |
Nefazodone |
50 μM |
|
bovine |
heart mitochondria |
Measurement of complex IV activity |
decrease |
Positive |
p < 0.001 |
3 |
Nefazodone |
50 μM |
|
bovine |
heart mitochondria |
Measurement of complex V activity |
decrease |
Positive |
p < 0.001 |
3 |
paroxetine |
50 μM |
|
bovine |
heart mitochondria |
Measurement of complex I activity |
decrease |
Positive |
p < 0.01 |
3 |
paroxetine |
50 μM |
|
bovine |
heart mitochondria |
Measurement of complex II + III activity |
decrease |
Positive |
p < 0.001 |
3 |
paroxetine |
50 μM |
|
bovine |
heart mitochondria |
Measurement of complex II + III activity |
decrease |
Positive |
p < 0.001 |
3 |
paroxetine |
50 μM |
|
bovine |
heart mitochondria |
Measurement of complex V activity |
decrease |
Positive |
p < 0.001 |
3 |
Simvastatin |
50 μM |
|
bovine |
heart mitochondria |
Measurement of complex I activity |
decrease |
Positive |
p < 0.01 |
3 |
Simvastatin |
50 μM |
|
bovine |
heart mitochondria |
Measurement of complex II + III activity |
decrease |
Positive |
p < 0.001 |
3 |
Simvastatin |
50 μM |
|
bovine |
heart mitochondria |
Measurement of complex II + III activity |
decrease |
Positive |
p < 0.001 |
3 |
Simvastatin |
50 μM |
|
bovine |
heart mitochondria |
Measurement of complex IV activity |
decrease |
Positive |
p < 0.001 |
3 |
Simvastatin |
50 μM |
|
bovine |
heart mitochondria |
Measurement of complex V activity |
decrease |
Positive |
p < 0.001 |
3 |
Tamoxifen |
50 μM |
|
bovine |
heart mitochondria |
Measurement of complex II + III activity |
decrease |
Positive |
p < 0.001 |
3 |
Tamoxifen |
50 μM |
|
bovine |
heart mitochondria |
Measurement of complex II + III activity |
decrease |
Positive |
p < 0.001 |
3 |
Tamoxifen |
50 μM |
|
bovine |
heart mitochondria |
Measurement of complex IV activity |
decrease |
Positive |
p < 0.001 |
3 |
Tamoxifen |
50 μM |
|
bovine |
heart mitochondria |
Measurement of complex V activity |
decrease |
Positive |
p < 0.001 |
3 |
Tamoxifen |
15 μM |
|
bovine |
heart mitochondria |
Measurement of complex II + III activity |
decrease |
Positive |
IC50 |
3 |
Tamoxifen |
15 μM |
|
bovine |
heart mitochondria |
Measurement of complex II + III activity |
decrease |
Positive |
IC50 |
3 |
Tamoxifen |
26.6 μM |
|
bovine |
heart mitochondria |
Measurement of complex IV activity |
decrease |
Positive |
IC50 |
3 |
Tamoxifen |
8.1 μM |
|
bovine |
heart mitochondria |
Measurement of complex V activity |
decrease |
Positive |
IC50 |
3 |
Tamoxifen |
4 μM |
|
bovine |
heart mitochondria |
Measurement of complex I activity |
decrease |
Positive |
IC50 |
3 |
Tamoxifen |
1.6 μM |
|
bovine |
heart mitochondria |
Measurement of complex V activity |
decrease |
Positive |
IC50 |
3 |
Tamoxifen |
30 μM |
|
bovine |
heart mitochondria |
Measurement of complex II + III activity |
decrease |
Positive |
IC50 |
3 |
Tamoxifen |
30 μM |
|
bovine |
heart mitochondria |
Measurement of complex II + III activity |
decrease |
Positive |
IC50 |
3 |
Tamoxifen |
29 μM |
|
bovine |
heart mitochondria |
Measurement of complex V activity |
decrease |
Positive |
IC50 |
3 |
Tamoxifen |
26 μM |
|
bovine |
heart mitochondria |
Measurement of complex V activity |
decrease |
Positive |
IC50 |
3 |
Amiodarone |
100 μmol/L |
|
rat; Sprague–Dawley |
liver mitochondria |
Measurement of oxygen uptake |
decrease |
Positive |
p < 0.01 |
4 |
Amiodarone |
10 μmol/L |
|
rat; Sprague–Dawley |
liver mitochondria |
Measurement of oxygen uptake |
decrease |
Positive |
p < 0.01 |
4 |
Amiodarone |
20 μmol/L |
|
rat; Sprague–Dawley |
liver mitochondria |
Measurement of oxygen uptake |
decrease |
Positive |
p < 0.01 |
4 |
Amiodarone |
50 μmol/L |
|
rat; Sprague–Dawley |
liver mitochondria |
Measurement of oxygen uptake |
decrease |
Positive |
p < 0.01 |
4 |
Amiodarone |
100 μmol/L |
|
rat; Sprague–Dawley |
liver mitochondria |
Measurement of oxygen uptake |
decrease |
Positive |
p < 0.01 |
4 |
benzarone |
100 μmol/L |
|
rat; Sprague–Dawley |
liver mitochondria |
Measurement of oxygen uptake |
decrease |
Positive |
p < 0.01 |
4 |
benzbromarone |
100 μmol/L |
|
rat; Sprague–Dawley |
liver mitochondria |
Measurement of oxygen uptake |
decrease |
Positive |
p < 0.01 |
4 |
benzbromarone |
1 μmol/L |
|
rat; Sprague–Dawley |
liver mitochondria |
Measurement of oxygen uptake |
decrease |
Positive |
p < 0.01 |
4 |
benzbromarone |
10 μmol/L |
|
rat; Sprague–Dawley |
liver mitochondria |
Measurement of oxygen uptake |
decrease |
Positive |
p < 0.01 |
4 |
benzbromarone |
100 μmol/L |
|
rat; Sprague–Dawley |
liver mitochondria |
Measurement of oxygen uptake |
decrease |
Positive |
p < 0.01 |
4 |
2‐Butylbenzofuran |
50 μmol/L |
|
rat; Sprague–Dawley |
liver mitochondria |
Measurement of oxygen uptake |
decrease |
Positive |
p < 0.05 |
4 |
2‐Butylbenzofuran |
100 μmol/L |
|
rat; Sprague–Dawley |
liver mitochondria |
Measurement of oxygen uptake |
decrease |
Positive |
p < 0.01 |
4 |
Amiodarone |
10 μmol/L |
|
rat; Sprague–Dawley |
liver mitochondria |
Measurement of oxygen uptake |
decrease |
Positive |
p < 0.01 |
4 |
Amiodarone |
20 μmol/L |
|
rat; Sprague–Dawley |
liver mitochondria |
Measurement of oxygen uptake |
decrease |
Positive |
p < 0.01 |
4 |
Amiodarone |
50 μmol/L |
|
rat; Sprague–Dawley |
liver mitochondria |
Measurement of oxygen uptake |
decrease |
Positive |
p < 0.01 |
4 |
Amiodarone |
100 μmol/L |
|
rat; Sprague–Dawley |
liver mitochondria |
Measurement of oxygen uptake |
decrease |
Positive |
p < 0.01 |
4 |
benzarone |
100 μmol/L |
|
rat; Sprague–Dawley |
liver mitochondria |
Measurement of oxygen uptake |
decrease |
Positive |
p < 0.01 |
4 |
benzarone |
20 μmol/L |
|
rat; Sprague–Dawley |
liver mitochondria |
Measurement of oxygen uptake |
decrease |
Positive |
p < 0.01 |
4 |
benzarone |
50 μmol/L |
|
rat; Sprague–Dawley |
liver mitochondria |
Measurement of oxygen uptake |
decrease |
Positive |
p < 0.01 |
4 |
benzarone |
100 μmol/L |
|
rat; Sprague–Dawley |
liver mitochondria |
Measurement of oxygen uptake |
decrease |
Positive |
p < 0.01 |
4 |
benzbromarone |
100 μmol/L |
|
rat; Sprague–Dawley |
liver mitochondria |
Measurement of oxygen uptake |
decrease |
Positive |
p < 0.01 |
4 |
benzbromarone |
0.1 μmol/L |
|
rat; Sprague–Dawley |
liver mitochondria |
Measurement of oxygen uptake |
decrease |
Positive |
p < 0.01 |
4 |
benzbromarone |
1 μmol/L |
|
rat; Sprague–Dawley |
liver mitochondria |
Measurement of oxygen uptake |
decrease |
Positive |
p < 0.01 |
4 |
benzbromarone |
10 μmol/L |
|
rat; Sprague–Dawley |
liver mitochondria |
Measurement of oxygen uptake |
decrease |
Positive |
p < 0.01 |
4 |
benzbromarone |
100 μmol/L |
|
rat; Sprague–Dawley |
liver mitochondria |
Measurement of oxygen uptake |
decrease |
Positive |
p < 0.01 |
4 |
2‐Butylbenzofuran |
100 μmol/L |
|
rat; Sprague–Dawley |
liver mitochondria |
Measurement of oxygen uptake |
decrease |
Positive |
p < 0.01 |
4 |
Amiodarone |
20 μmol/L |
|
rat; Sprague–Dawley |
liver mitochondria |
Measurement of beta oxidation and ketone body formation |
decrease |
Positive |
p < 0.01 |
4 |
Amiodarone |
50 μmol/L |
|
rat; Sprague–Dawley |
liver mitochondria |
Measurement of beta oxidation and ketone body formation |
decrease |
Positive |
p < 0.01 |
4 |
Amiodarone |
80 μmol/L |
|
rat; Sprague–Dawley |
liver mitochondria |
Measurement of beta oxidation and ketone body formation |
decrease |
Positive |
p < 0.01 |
4 |
Amiodarone |
100 μmol/L |
|
rat; Sprague–Dawley |
liver mitochondria |
Measurement of beta oxidation and ketone body formation |
decrease |
Positive |
p < 0.01 |
4 |
benzarone |
20 μmol/L |
|
rat; Sprague–Dawley |
liver mitochondria |
Measurement of beta oxidation and ketone body formation |
decrease |
Positive |
p < 0.01 |
4 |
benzarone |
50 μmol/L |
|
rat; Sprague–Dawley |
liver mitochondria |
Measurement of beta oxidation and ketone body formation |
decrease |
Positive |
p < 0.01 |
4 |
benzarone |
100 μmol/L |
|
rat; Sprague–Dawley |
liver mitochondria |
Measurement of beta oxidation and ketone body formation |
decrease |
Positive |
p < 0.01 |
4 |
benzbromarone |
2 μmol/L |
|
rat; Sprague–Dawley |
liver mitochondria |
Measurement of beta oxidation and ketone body formation |
decrease |
Positive |
p < 0.05 |
4 |
benzbromarone |
5 μmol/L |
|
rat; Sprague–Dawley |
liver mitochondria |
Measurement of beta oxidation and ketone body formation |
decrease |
Positive |
p < 0.01 |
4 |
benzbromarone |
10 μmol/L |
|
rat; Sprague–Dawley |
liver mitochondria |
Measurement of beta oxidation and ketone body formation |
decrease |
Positive |
p < 0.01 |
4 |
benzbromarone |
50 μmol/L |
|
rat; Sprague–Dawley |
liver mitochondria |
Measurement of beta oxidation and ketone body formation |
decrease |
Positive |
p < 0.01 |
4 |
2‐Butylbenzofuran |
100 μmol/L |
|
rat; Sprague–Dawley |
liver mitochondria |
Measurement of beta oxidation and ketone body formation |
decrease |
Positive |
p < 0.01 |
4 |
Amiodarone |
34 μmol/L |
|
rat; Sprague–Dawley |
liver mitochondria |
Measurement of beta oxidation and ketone body formation |
decrease |
Positive |
IC50 |
4 |
benzarone |
34 μmol/L |
|
rat; Sprague–Dawley |
liver mitochondria |
Measurement of beta oxidation and ketone body formation |
decrease |
Positive |
IC50 |
4 |
benzbromarone |
2 μmol/L |
|
rat; Sprague–Dawley |
liver mitochondria |
Measurement of beta oxidation and ketone body formation |
decrease |
Positive |
IC50 |
4 |
2‐Butylbenzofuran |
100 μmol/L |
|
rat; Sprague–Dawley |
liver mitochondria |
Measurement of beta oxidation and ketone body formation |
decrease |
Positive |
28% inhibition |
4 |
Amiodarone |
100 μmol/L |
|
rat; Sprague–Dawley |
liver mitochondria |
Measurement of acyl‐CoA dehydrogenase activity |
decrease |
Positive |
28% inhibition |
4 |
benzarone |
100 μmol/L |
|
rat; Sprague–Dawley |
liver mitochondria |
Measurement of acyl‐CoA dehydrogenase activity |
decrease |
Positive |
33% inhibition |
4 |
benzbromarone |
100 μmol/L |
|
rat; Sprague–Dawley |
liver mitochondria |
Measurement of acyl‐CoA dehydrogenase activity |
decrease |
Positive |
34% inhibition |
4 |
2‐Butylbenzofuran |
100 μmol/L |
|
rat; Sprague–Dawley |
liver mitochondria |
Measurement of acyl‐CoA dehydrogenase activity |
decrease |
Positive |
22% inhibition |
4 |
benzarone |
100 μmol/L |
|
rat; Sprague–Dawley |
liver mitochondria |
Measurement of β‐ketothiolase activity |
decrease |
Positive |
11% inhibition |
4 |
benzbromarone |
100 μmol/L |
|
rat; Sprague–Dawley |
liver mitochondria |
Measurement of β‐ketothiolase activity |
decrease |
Positive |
25% inhibition |
4 |
Diclofenac |
50 μmol/L |
2 minutes |
rat |
liver mitochondria |
Assessment of Mitochondrial Ca2+ Efflux; Energized with succinate |
decrease |
Positive |
not mentioned |
6 |
Diclofenac |
50 μmol/L |
10 minutes |
rat |
liver mitochondria |
Measurement of Mitochondrial NADPH; incubated in the presence of Ca2+ |
increase |
Positive |
p < 0.01 |
6 |
Diclofenac |
50 μmol/L |
10 minutes |
rat |
liver mitochondria |
Assay of Mitochondrial Protein Thiol; Assay of Mitochondrial GSH; incubated in the presence of Ca2+ |
decrease |
Positive |
p < 0.01 |
6 |
Diclofenac |
250 μmol/L |
24 hours |
rat |
hepatocytes |
Assay of Cellular ATP contents; Assay of LDH leakage |
decrease |
Positive |
p < 0.01 |
6 |
Diclofenac |
500 μmol/L |
24 hours |
rat |
hepatocytes |
Assay of Cellular ATP contents; Assay of LDH leakage |
decrease |
Positive |
p < 0.01 |
6 |
Rotenone |
263±43 nM |
2 minutes |
human |
HepG2 |
Measurement of OCR |
decrease |
Positive |
EC50 |
7 |
Rotenone |
371±58 nM |
2 minutes |
human |
HepG2 |
Measurement of ECAR |
increase |
Positive |
EC50 |
7 |
Antimycin A |
4±0.2 nM |
2 minutes |
human |
HepG2 |
Measurement of OCR |
decrease |
Positive |
EC50 |
7 |
Antimycin A |
100±20 nM |
2 minutes |
human |
HepG2 |
Measurement of ECAR |
increase |
Positive |
EC50 |
7 |
Oligomycin |
0.92± 0.18 μM |
2 minutes |
human |
HepG2 |
Measurement of OCR |
decrease |
Positive |
EC50 |
7 |
Oligomycin |
1.1±0.23 μM |
2 minutes |
human |
HepG2 |
Measurement of ECAR |
increase |
Positive |
EC50 |
7 |
FCCP |
54±7 nM |
2 minutes |
human |
HepG2 |
Measurement of OCR |
increase |
Positive |
EC50 |
7 |
FCCP |
141±20 nM |
2 minutes |
human |
HepG2 |
Measurement of ECAR |
increase |
Positive |
EC50 |
7 |
2-Deoxy-D-glucose |
150 mM |
2 minutes |
human |
HepG2 |
Measurement of OCR |
increase |
Positive |
EC50 |
7 |
2-Deoxy-D-glucose |
150 mM |
2 minutes |
human |
HepG2 |
Measurement of ECAR |
decrease |
Positive |
EC50 |
7 |
Tolcapone |
3.7 μM |
2 minutes |
human |
HepG2 |
Measurement of OCR |
increase |
Positive |
EC50 |
7 |
Tolcapone |
3.7 μM |
2 minutes |
human |
HepG2 |
Measurement of ECAR |
increase |
Positive |
EC50 |
7 |
Entacapone |
33 μM |
2 minutes |
human |
HepG2 |
Measurement of OCR |
increase |
Positive |
EC50 |
7 |
Entacapone |
100 μM |
2 minutes |
human |
HepG2 |
Measurement of ECAR |
increase |
Positive |
EC50 |
7 |
Nilutamide |
66 μM |
2 minutes |
human |
HepG2 |
Measurement of OCR |
decrease |
Positive |
EC50 |
7 |
Nilutamide |
79 μM |
2 minutes |
human |
HepG2 |
Measurement of ECAR |
increase |
Positive |
EC50 |
7 |
Flutamide |
> 100 μM |
2 minutes |
human |
HepG2 |
Measurement of OCR |
decrease |
Positive |
EC50 |
7 |
Flutamide |
> 100 μM |
2 minutes |
human |
HepG2 |
Measurement of ECAR |
increase |
Positive |
EC50 |
7 |
Chlorpromazine |
> 300 μM |
2 minutes |
human |
HepG2 |
Measurement of OCR |
increase |
Positive |
EC50 |
7 |
Chlorpromazine |
> 300 μM |
2 minutes |
human |
HepG2 |
Measurement of ECAR |
increase |
Positive |
EC50 |
7 |
Diflunisal |
15 μM |
2 minutes |
human |
HepG2 |
Measurement of OCR |
increase |
Positive |
EC50 |
7 |
Diflunisal |
30 μM |
2 minutes |
human |
HepG2 |
Measurement of ECAR |
increase |
Positive |
EC50 |
7 |
Benoxaprofen |
30 μM |
2 minutes |
human |
HepG2 |
Measurement of ECAR |
decrease |
Positive |
EC50 |
7 |
Benoxaprofen |
> 100 μM |
2 minutes |
human |
HepG2 |
Measurement of ECAR |
increase |
Positive |
EC50 |
7 |
Troglitazone |
> 100 μM |
2 minutes |
human |
HepG2 |
Measurement of ECAR |
decrease |
Positive |
EC50 |
7 |
Troglitazone |
> 100 μM |
2 minutes |
human |
HepG2 |
Measurement of ECAR |
increase |
Positive |
EC50 |
7 |
Ciglitazone |
> 100 μM |
2 minutes |
human |
HepG2 |
Measurement of ECAR |
decrease |
Positive |
EC50 |
7 |
Ciglitazone |
> 100 μM |
2 minutes |
human |
HepG2 |
Measurement of ECAR |
increase |
Positive |
EC50 |
7 |
Troglitazone |
10 μM |
2 minutes |
feline |
cardiomyocytes |
Measurement of OCR |
increase |
Positive |
EC50 |
7 |
Troglitazone |
10 μM |
2 minutes |
feline |
cardiomyocytes |
Measurement of ECAR |
increase |
Positive |
EC50 |
7 |
Ciglitazone |
> 100 μM |
2 minutes |
feline |
cardiomyocytes |
Measurement of OCR |
decrease |
Positive |
EC50 |
7 |
Ciglitazone |
10 μM |
2 minutes |
feline |
cardiomyocytes |
Measurement of ECAR |
increase |
Positive |
EC50 |
7 |
Rosiglitazone |
> 100 μM |
2 minutes |
feline |
cardiomyocytes |
Measurement of OCR |
increase |
Positive |
EC50 |
7 |
Rosiglitazone |
> 100 μM |
2 minutes |
feline |
cardiomyocytes |
Measurement of ECAR |
increase |
Positive |
EC50 |
7 |
Metformin |
5 mM |
24 hours |
human |
MCF7 |
Meassurement of mitochondrial respiration |
decrease |
Positive |
p < 0.05 |
172 |
Metformin |
0.5 mM |
24 hours |
human |
MCF7 |
Meassurement of coupled respiration |
decrease |
Positive |
p < 0.05 |
172 |
Metformin |
5 mM |
24 hours |
human |
MCF7 |
Meassurement of coupled respiration |
decrease |
Positive |
p < 0.05 |
172 |
Metformin |
0.5 mM |
24 hours |
human |
MCF7 |
Meassurement of non-mitochondrial respiration |
increase |
Positive |
p < 0.05 |
172 |
Metformin |
5 mM |
24 hours |
human |
MCF7 |
Meassurement of non-mitochondrial respiration |
increase |
Positive |
p < 0.05 |
172 |
Metformin |
0.5 mM |
24 hours |
human |
MCF7 |
Meassurement of coupled respiration; Meassurement of uncoupled respiration; cells grown in glucose |
increase |
Positive |
p < 0.05 |
172 |
Metformin |
0.5 mM |
24 hours |
human |
MCF7 |
Meassurement of coupled respiration; Meassurement of uncoupled respiration; cells grown in galactose |
increase |
Positive |
p < 0.05 |
172 |
Metformin |
0.5 mM |
24 hours |
mouse |
NMuMG |
Meassurement of mitochondrial respiration |
decrease |
Positive |
p < 0.05 |
172 |
Metformin |
0.5 mM |
24 hours |
mouse |
NT2196 |
Meassurement of mitochondrial respiration |
decrease |
Positive |
p < 0.05 |
172 |
Metformin |
0.5 mM |
24 hours |
human |
MCF10A |
Meassurement of mitochondrial respiration |
decrease |
Positive |
p < 0.05 |
172 |
Metformin |
0.5 mM |
24 hours |
human |
MCF7 |
Meassurement of mitochondrial respiration |
decrease |
Positive |
p < 0.05 |
172 |
Metformin |
0.5 mM |
24 hours |
mouse |
NMuMG |
Meassurement of coupled respiration; Meassurement of uncoupled respiration |
increase |
Positive |
p < 0.05 |
172 |
Metformin |
0.5 mM |
24 hours |
human |
MCF10A |
Meassurement of coupled respiration; Meassurement of uncoupled respiration |
increase |
Positive |
p < 0.05 |
172 |
Metformin |
5 mM |
24 hours |
mouse |
NMuMG |
Meassurement of glucose concentration |
increase |
Positive |
p < 0.05 |
172 |
Metformin |
5 mM |
24 hours |
mouse |
NT2196 |
Meassurement of glucose concentration |
increase |
Positive |
p < 0.05 |
172 |
Metformin |
5 mM |
24 hours |
human |
MCF10A |
Meassurement of glucose concentration |
increase |
Positive |
p < 0.05 |
172 |
Metformin |
5 mM |
24 hours |
human |
MCF7 |
Meassurement of glucose concentration |
increase |
Positive |
p < 0.05 |
172 |
Metformin |
5 mM |
24 hours |
mouse |
NT2196 |
Meassurement of lactate concentration |
increase |
Positive |
p < 0.05 |
172 |
Metformin |
5 mM |
24 hours |
human |
MCF10A |
Meassurement of lactate concentration |
increase |
Positive |
p < 0.05 |
172 |
Metformin |
5 mM |
24 hours |
human |
MCF7 |
Meassurement of lactate concentration |
increase |
Positive |
p < 0.05 |
172 |
Metformin |
5 mM |
48 hours |
mouse |
NMuMG |
Meassurement of glucose concentration |
increase |
Positive |
p < 0.05 |
172 |
Metformin |
5 mM |
48 hours |
mouse |
NT2196 |
Meassurement of glucose concentration |
increase |
Positive |
p < 0.05 |
172 |
Metformin |
5 mM |
48 hours |
human |
MCF10A |
Meassurement of glucose concentration |
increase |
Positive |
p < 0.05 |
172 |
Metformin |
5 mM |
48 hours |
human |
MCF7 |
Meassurement of glucose concentration |
increase |
Positive |
p < 0.05 |
172 |
Metformin |
5 mM |
48 hours |
mouse |
NMuMG |
Meassurement of lactate concentration |
increase |
Positive |
p < 0.05 |
172 |
Metformin |
5 mM |
48 hours |
mouse |
NT2196 |
Meassurement of lactate concentration |
increase |
Positive |
p < 0.05 |
172 |
Metformin |
5 mM |
48 hours |
human |
MCF10A |
Meassurement of lactate concentration |
increase |
Positive |
p < 0.05 |
172 |
Metformin |
5 mM |
48 hours |
human |
MCF7 |
Meassurement of lactate concentration |
increase |
Positive |
p < 0.05 |
172 |
Metformin |
0.5mM |
24 hours |
human |
MCF7 |
Meassurement of lactate + pyruvate concentration; compared with MCF10A |
increase |
Positive |
p < 0.05 |
172 |
Metformin |
5.0mM |
24 hours |
human |
MCF7 |
Meassurement of lactate + pyruvate concentration; compared with MCF10A |
increase |
Positive |
p < 0.05 |
172 |
Metformin |
0.5mM |
24 hours |
human |
MCF10A |
Meassurement of citrate concentration; compared with MCF10A |
affect |
Positive |
p < 0.05 |
172 |
Metformin |
0.5mM |
24 hours |
human |
MCF7 |
Meassurement of citrate concentration; compared with MCF10A |
affect |
Positive |
p < 0.05 |
172 |
Metformin |
0.5mM |
24 hours |
human |
MCF10A |
Meassurement of isocitrate concentration; compared with MCF10A |
affect |
Positive |
p < 0.05 |
172 |
Metformin |
0.5mM |
24 hours |
human |
MCF7 |
Meassurement of isocitrate concentration; compared with MCF10A |
affect |
Positive |
p < 0.05 |
172 |
Metformin |
0.5mM |
24 hours |
human |
MCF10A |
Meassurement of alpha-ketoglutarate concentration; compared with MCF10A |
affect |
Positive |
p < 0.05 |
172 |
Metformin |
0.5mM |
24 hours |
human |
MCF7 |
Meassurement of alpha-ketoglutarate concentration; compared with MCF10A |
affect |
Positive |
p < 0.05 |
172 |
Metformin |
2mM |
30 minutes |
mouse; C57BL/6J |
isolated skeletal muscle mitochondria |
Measurement of Oxygen level; incubated in complex I substrate; added ADP (500 μM) |
decrease |
Positive |
p < 0.05 |
172 |
Metformin |
2mM |
30 minutes |
mouse; C57BL/6J |
isolated skeletal muscle mitochondria |
Measurement of Oxygen level; incubated in complex I substrate; added oligomycin (2.5 μg oligomycin/mg mitochondrial protein) |
decrease |
Positive |
p < 0.05 |
172 |
Metformin |
2mM |
30 minutes |
mouse; C57BL/6J |
isolated skeletal muscle mitochondria |
Measurement of Oxygen level; incubated in complex I substrate; added FCCP (1.5 μM) |
decrease |
Positive |
p < 0.05 |
172 |
Metformin |
5mM |
30 minutes |
mouse; C57BL/6J |
isolated skeletal muscle mitochondria |
Meassurement of lactate concentration |
increase |
Positive |
p < 0.05 |
172 |
Metformin |
5mM |
30 minutes |
mouse; C57BL/6J |
isolated skeletal muscle mitochondria |
Meassurement of citrate concentration; compared with MCF10A |
affect |
Positive |
p < 0.05 |
172 |
Metformin |
5mM |
30 minutes |
mouse; C57BL/6J |
isolated skeletal muscle mitochondria |
Meassurement of citrate concentration; compared with MCF10A |
affect |
Positive |
p < 0.05 |
172 |
Metformin |
5mM |
30 minutes |
mouse; C57BL/6J |
isolated skeletal muscle mitochondria |
Meassurement of alpha-ketoglutarate concentration; compared with MCF10A |
affect |
Positive |
p < 0.05 |
172 |
Metformin |
5mM |
30 minutes |
mouse; C57BL/6J |
isolated skeletal muscle mitochondria |
Meassurement of alpha-ketoglutarate concentration; compared with MCF10A |
affect |
Positive |
p < 0.05 |
172 |
Metformin |
5mM |
30 minutes |
mouse; C57BL/6J |
isolated skeletal muscle mitochondria |
Meassurement of succinate concentration |
decrease |
Positive |
p < 0.05 |
172 |
Metformin |
5mM |
30 minutes |
mouse; C57BL/6J |
isolated skeletal muscle mitochondria |
Meassurement of succinate concentration |
decrease |
Positive |
p < 0.05 |
172 |
Nimesulide |
1 mM |
|
rat; Sprague-Dawley Crl:CD (SD) BR |
lung microsomes |
measurement of oxygen consumption |
increase |
Positive |
p < 0.05 |
11 |
Nimesulide |
1 mM |
|
rat; Sprague-Dawley Crl:CD (SD) BR |
lung microsomes |
measurement of NADPH oxidation |
increase |
Positive |
p < 0.05 |
11 |
Nitrofurantoin |
1 mM |
|
mouse; C57B/6J |
liver mitochondria |
Measurement of oxygen uptake; used glutamate as substrate |
decrease |
Positive |
p < 0.05; 61% inhibition |
13 |
Nitrofurantoin |
50 μM |
|
mouse; C57B/6J |
liver mitochondria |
Measurement of oxygen uptake; used glutamate as substrate |
decrease |
Positive |
p < 0.05; 72% inhibition |
13 |
Nitrofurantoin |
5 μM |
|
mouse; C57B/6J |
liver mitochondria |
Measurement of oxygen uptake; used glutamate as substrate |
decrease |
Positive |
p < 0.05; 38% inhibition |
13 |
Nitrofurantoin |
1 mM |
|
mouse; C57B/6J |
liver mitochondria |
Measurement of oxygen uptake; used β-hydroxybutyrate as substrate |
decrease |
Positive |
p < 0.05 |
13 |
Nitrofurantoin |
50 μM |
|
mouse; C57B/6J |
liver mitochondria |
Measurement of oxygen uptake; used β-hydroxybutyrate as substrate |
decrease |
Positive |
p < 0.05; 60% inhibition |
13 |
Nitrofurantoin |
5 μM |
|
mouse; C57B/6J |
liver mitochondria |
Measurement of oxygen uptake; used β-hydroxybutyrate as substrate |
decrease |
Positive |
p < 0.05 |
13 |
Nitrofurantoin |
1 mM |
|
mouse; C57B/6J |
liver mitochondria |
Measurement of oxygen uptake; used α-ketoghttarate as substrate |
decrease |
Positive |
p < 0.05 |
13 |
Nitrofurantoin |
50 μM |
|
mouse; C57B/6J |
liver mitochondria |
Measurement of oxygen uptake; used α-ketoghttarate as substrate |
decrease |
Positive |
p < 0.05; 70% inhibition |
13 |
Nitrofurantoin |
5 μM |
|
mouse; C57B/6J |
liver mitochondria |
Measurement of oxygen uptake; used α-ketoghttarate as substrate |
decrease |
Positive |
p < 0.05 |
13 |
nitrofurazone |
1mM |
|
mouse; C57B/6J |
liver mitochondria |
Measurement of oxygen uptake |
decrease |
Positive |
p < 0.05; 64% inhibition |
13 |
nitrofurazone |
1mM |
|
mouse; C57B/6J |
liver mitochondria |
Measurement of oxygen uptake |
decrease |
Positive |
p < 0.05; 63% inhibition |
13 |
Nitrofurantoin |
1 mM |
|
mouse; C57B/6J |
liver mitochondria |
Measurement of oxygen uptake |
decrease |
Positive |
p < 0.05 |
13 |
Nitrofurantoin |
0.005mM |
|
mouse; C57B/6J |
liver mitochondria |
Measurement of oxygen uptake |
decrease |
Positive |
p < 0.05 |
13 |
Nitrofurantoin |
1 mM |
|
mouse; C57B/6J |
liver mitochondria |
Measurement of oxygen uptake |
decrease |
Positive |
p < 0.05 |
13 |
Nitrofurantoin |
0.05mM |
|
mouse; C57B/6J |
liver mitochondria |
Measurement of oxygen uptake |
decrease |
Positive |
p < 0.05 |
13 |
Nitrofurantoin |
1 mM |
|
mouse; C57B/6J |
liver mitochondria |
Measurement of oxygen uptake |
decrease |
Positive |
p < 0.05 |
13 |
Nitrofurantoin |
0.05mM |
|
mouse; C57B/6J |
liver mitochondria |
Measurement of oxygen uptake |
decrease |
Positive |
p < 0.05 |
13 |
nitrofurazone |
1mM |
|
mouse; C57B/6J |
liver mitochondria |
Measurement of oxygen uptake |
decrease |
Positive |
p < 0.05 |
13 |
nitrofurazone |
1mM |
|
mouse; C57B/6J |
liver mitochondria |
Measurement of oxygen uptake |
decrease |
Positive |
p < 0.05 |
13 |
nitrofurazone |
5μM |
|
mouse; C57B/6J |
mitoplasts |
Measurement of oxygen uptake |
decrease |
Positive |
p < 0.05 |
13 |
nitrofurazone |
5μM |
|
mouse; C57B/6J |
mitoplasts |
Measurement of oxygen uptake |
decrease |
Positive |
p < 0.05 |
13 |
buformin |
62.5 μM |
24 hours |
human |
HepG2 cells |
Assay of Cellular ATP Content |
decrease |
Positive |
p < 0.001 |
15 |
buformin |
62.5 μM |
24 hours |
human |
HepG2 cells |
Assay of Cellular ATP Content |
decrease |
Positive |
p < 0.001 |
15 |
Phenformin |
62.5 μM |
24 hours |
human |
HepG2 cells |
Assay of Cellular ATP Content |
decrease |
Positive |
p < 0.001 |
15 |
Phenformin |
62.5 μM |
24 hours |
human |
HepG2 cells |
Assay of Cellular ATP Content |
decrease |
Positive |
p < 0.001 |
15 |
Metformin |
657 μM |
24 hours |
human |
hepatocytes |
Assay of Cellular ATP Content |
decrease |
Positive |
IC50 |
15 |
buformin |
26.1 μM |
24 hours |
human |
hepatocytes |
Assay of Cellular ATP Content |
decrease |
Positive |
IC50 |
15 |
Phenformin |
11.7 μM |
24 hours |
human |
hepatocytes |
Assay of Cellular ATP Content |
decrease |
Positive |
IC50 |
15 |
Metformin |
1430 μM |
24 hours |
human |
HepG2 cells |
Assay of Cellular ATP Content |
decrease |
Positive |
IC50 |
15 |
buformin |
43.7 μM |
24 hours |
human |
HepG2 cells |
Assay of Cellular ATP Content |
decrease |
Positive |
IC50 |
15 |
Phenformin |
12.9 μM |
24 hours |
human |
HepG2 cells |
Assay of Cellular ATP Content |
decrease |
Positive |
IC50 |
15 |
Metformin |
> 2000 μM |
24 hours |
human |
HepG2 cells |
Assay of Cellular ATP Content |
decrease |
Positive |
IC50 |
15 |
buformin |
> 500 μM |
24 hours |
human |
HepG2 cells |
Assay of Cellular ATP Content |
decrease |
Positive |
IC50 |
15 |
Phenformin |
> 500 μM |
24 hours |
human |
HepG2 cells |
Assay of Cellular ATP Content |
decrease |
Positive |
IC50 |
15 |
buformin |
25 μM |
24 hours |
human |
HepG2 cells |
Measurement of OCR |
decrease |
Positive |
p < 0.001 |
15 |
Phenformin |
25 μM |
24 hours |
human |
HepG2 cells |
Measurement of OCR |
decrease |
Positive |
p < 0.001 |
15 |
buformin |
25 μM |
24 hours |
human |
HepG2 cells |
Measurement of ECAR |
increase |
Positive |
p < 0.001 |
15 |
Phenformin |
25 μM |
24 hours |
human |
HepG2 cells |
Measurement of ECAR |
increase |
Positive |
p < 0.001 |
15 |
buformin |
100 nmol/mg mitochondrial protein |
|
rat; Sprague–Dawley |
liver mitochondria |
Meassurement of respiration |
decrease |
Positive |
|
15 |
Phenformin |
100 nmol/mg mitochondrial protein |
|
rat; Sprague–Dawley |
liver mitochondria |
Meassurement of respiration |
decrease |
Positive |
|
15 |
Metformin |
500 nmol/mg mitochondrial protein |
40 minutes preincubation |
rat; Sprague–Dawley |
liver mitochondria |
Meassurement of respiration |
decrease |
Positive |
|
15 |
buformin |
100 nmol/mg mitochondrial protein |
40 minutes preincubation |
rat; Sprague–Dawley |
liver mitochondria |
Meassurement of respiration |
decrease |
Positive |
|
15 |
Phenformin |
100 nmol/mg mitochondrial protein |
40 minutes preincubation |
rat; Sprague–Dawley |
liver mitochondria |
Meassurement of respiration |
decrease |
Positive |
|
15 |
buformin |
100 nmol/mg mitochondrial protein |
|
rat; Sprague–Dawley |
liver mitochondria |
Meassurement of respiration |
decrease |
Positive |
|
15 |
Phenformin |
100 nmol/mg mitochondrial protein |
|
rat; Sprague–Dawley |
liver mitochondria |
Meassurement of respiration |
decrease |
Positive |
|
15 |
Metformin |
500 nmol/mg mitochondrial protein |
40 min preincubation |
rat; Sprague–Dawley |
liver mitochondria |
Meassurement of respiration |
decrease |
Positive |
|
15 |
buformin |
100 nmol/mg mitochondrial protein |
40 min preincubation |
rat; Sprague–Dawley |
liver mitochondria |
Meassurement of respiration |
decrease |
Positive |
|
15 |
Phenformin |
100 nmol/mg mitochondrial protein |
40 min preincubation |
rat; Sprague–Dawley |
liver mitochondria |
Meassurement of respiration |
decrease |
Positive |
|
15 |
Metformin |
66 mM |
|
Bovine |
heart mitochondria |
Measurement of complex I activity |
decrease |
Positive |
IC50 |
15 |
buformin |
11.3 mM |
|
Bovine |
heart mitochondria |
Measurement of complex I activity |
decrease |
Positive |
IC50 |
15 |
Phenformin |
1.2 mM |
|
Bovine |
heart mitochondria |
Measurement of complex I activity |
decrease |
Positive |
IC50 |
15 |
Perhexiline |
5 μM |
72 hours |
rat; Sprague-Dawley Crl:CD-1 (ICR) BR |
hepatocytes |
Measurement of beta oxidation |
decrease |
Positive |
p < 0.05 |
193 |
Perhexiline |
25 μM |
24 hours |
rat; Sprague-Dawley Crl:CD-1 (ICR) BR |
hepatocytes |
Measurement of beta oxidation |
decrease |
Positive |
p < 0.05 |
193 |
Perhexiline |
100 μM |
|
mouse; Crl/CD-l(1CR)BR Swiss |
liver mitochondria |
Measurement of oxygen uptake |
increase |
Positive |
p < 0.01 |
193 |
Perhexiline |
200 μM |
|
mouse; Crl/CD-l(1CR)BR Swiss |
liver mitochondria |
Measurement of oxygen uptake |
increase |
Positive |
p < 0.01 |
193 |
Perhexiline |
100 μM |
|
mouse; Crl/CD-l(1CR)BR Swiss |
liver mitochondria |
Measurement of oxygen uptake |
increase |
Positive |
p < 0.01 |
193 |
Perhexiline |
200 μM |
|
mouse; Crl/CD-l(1CR)BR Swiss |
liver mitochondria |
Measurement of oxygen uptake |
increase |
Positive |
p < 0.01 |
193 |
Perhexiline |
100 μM |
5 minutes preincubation |
mouse; Crl/CD-l(1CR)BR Swiss |
liver mitochondria |
Measurement of oxygen uptake |
decrease |
Positive |
p < 0.01 |
193 |
Perhexiline |
200 μM |
5 minutes preincubation |
mouse; Crl/CD-l(1CR)BR Swiss |
liver mitochondria |
Measurement of oxygen uptake |
decrease |
Positive |
p < 0.01 |
193 |
Perhexiline |
400 μM |
5 minutes preincubation |
mouse; Crl/CD-l(1CR)BR Swiss |
liver mitochondria |
Measurement of oxygen uptake |
decrease |
Positive |
p < 0.01 |
193 |
Perhexiline |
100 μM |
5 minutes preincubation |
mouse; Crl/CD-l(1CR)BR Swiss |
liver mitochondria |
Measurement of oxygen uptake |
decrease |
Positive |
p < 0.05 |
193 |
Perhexiline |
200 μM |
5 minutes preincubation |
mouse; Crl/CD-l(1CR)BR Swiss |
liver mitochondria |
Measurement of oxygen uptake |
decrease |
Positive |
p < 0.01 |
193 |
Perhexiline |
400 μM |
5 minutes preincubation |
mouse; Crl/CD-l(1CR)BR Swiss |
liver mitochondria |
Measurement of oxygen uptake |
decrease |
Positive |
p < 0.01 |
193 |
Perhexiline |
200 μM |
5 minutes preincubation |
mouse; Crl/CD-l(1CR)BR Swiss |
liver mitochondria |
Measurement of oxygen uptake |
decrease |
Positive |
p < 0.01 |
193 |
Perhexiline |
100 μM |
5 minutes preincubation; 10 minutes |
mouse; Crl/CD-l(1CR)BR Swiss |
liver mitochondria |
Measurement of beta oxidation |
decrease |
Positive |
p < 0.01 |
193 |
Perhexiline |
100 μM |
5 minutes preincubation; 10 minutes |
mouse; Crl/CD-l(1CR)BR Swiss |
liver mitochondria |
Measurement of beta oxidation |
decrease |
Positive |
p < 0.01 |
193 |
Perhexiline |
200 μM |
|
mouse; Crl/CD-l(1CR)BR Swiss |
liver mitochondria |
Measurement of activities of acyl-CoA dehydrogenases |
decrease |
Positive |
p < 0.01 |
193 |
Perhexiline |
400 μM |
|
mouse; Crl/CD-l(1CR)BR Swiss |
liver mitochondria |
Measurement of activities of acyl-CoA dehydrogenases |
decrease |
Positive |
p < 0.01 |
193 |
Perhexiline |
800 μM |
|
mouse; Crl/CD-l(1CR)BR Swiss |
liver mitochondria |
Measurement of activities of acyl-CoA dehydrogenases |
decrease |
Positive |
p < 0.01 |
193 |
Perhexiline |
1200 μM |
|
mouse; Crl/CD-l(1CR)BR Swiss |
liver mitochondria |
Measurement of activities of acyl-CoA dehydrogenases |
decrease |
Positive |
p < 0.01 |
193 |
Perhexiline |
200 μM |
|
mouse; Crl/CD-l(1CR)BR Swiss |
liver mitochondria |
Measurement of activities of acyl-CoA dehydrogenases |
decrease |
Positive |
p < 0.01 |
193 |
Perhexiline |
400 μM |
|
mouse; Crl/CD-l(1CR)BR Swiss |
liver mitochondria |
Measurement of activities of acyl-CoA dehydrogenases |
decrease |
Positive |
p < 0.01 |
193 |
Perhexiline |
800 μM |
|
mouse; Crl/CD-l(1CR)BR Swiss |
liver mitochondria |
Measurement of activities of acyl-CoA dehydrogenases |
decrease |
Positive |
p < 0.01 |
193 |
Perhexiline |
1200 μM |
|
mouse; Crl/CD-l(1CR)BR Swiss |
liver mitochondria |
Measurement of activities of acyl-CoA dehydrogenases |
decrease |
Positive |
p < 0.01 |
193 |
Perhexiline |
1600 μM |
|
mouse; Crl/CD-l(1CR)BR Swiss |
liver mitochondria |
Measurement of activities of acyl-CoA dehydrogenases |
decrease |
Positive |
p < 0.01 |
193 |
Perhexiline |
400 μM |
|
mouse; Crl/CD-l(1CR)BR Swiss |
liver mitochondria |
Measurement of activities of acyl-CoA dehydrogenases |
decrease |
Positive |
p < 0.05 |
193 |
Perhexiline |
800 μM |
|
mouse; Crl/CD-l(1CR)BR Swiss |
liver mitochondria |
Measurement of activities of acyl-CoA dehydrogenases |
decrease |
Positive |
p < 0.01 |
193 |
Perhexiline |
1200 μM |
|
mouse; Crl/CD-l(1CR)BR Swiss |
liver mitochondria |
Measurement of activities of acyl-CoA dehydrogenases |
decrease |
Positive |
p < 0.01 |
193 |
Perhexiline |
1600 μM |
|
mouse; Crl/CD-l(1CR)BR Swiss |
liver mitochondria |
Measurement of activities of acyl-CoA dehydrogenases |
decrease |
Positive |
p < 0.01 |
193 |
Perhexiline |
|
|
|
|
|
decrease |
Positive |
|
16 |
Perhexiline |
|
|
|
|
|
decrease |
Positive |
|
16 |
Perhexiline |
|
|
|
|
|
decrease |
Positive |
|
16 |
Perhexiline |
|
|
|
|
|
decrease |
Positive |
|
16 |
Perhexiline |
|
|
|
|
|
decrease |
Positive |
|
17 |
Perhexiline |
|
|
|
|
|
decrease |
Positive |
|
17 |
Trimetazidine |
|
|
|
|
|
decrease |
Positive |
|
17 |
Trimetazidine |
|
|
|
|
|
increase |
Positive |
|
17 |
ranolazine |
|
|
|
|
|
increase |
Positive |
|
17 |
ranolazine |
|
|
|
|
|
decrease |
Positive |
|
17 |
Pioglitazone |
|
|
|
|
|
|
Positive |
|
21 |
Pioglitazone |
|
|
|
|
|
decrease |
Positive |
|
22 |
Pioglitazone |
|
|
|
|
|
decrease |
Positive |
|
22 |
promethazine |
|
|
|
|
|
increase |
Positive |
|
22 |
promethazine |
|
|
|
|
|
increase |
Positive |
|
22 |
clomipramine |
|
|
|
|
|
increase |
Positive |
|
22 |
clomipramine |
|
|
|
|
|
decrease |
Positive |
|
22 |
clomipramine |
|
|
|
|
|
increase |
Positive |
|
22 |
imipramine |
|
|
|
|
|
increase |
Positive |
|
22 |
imipramine |
|
|
|
|
|
increase |
Positive |
|
22 |
Chlorpromazine |
|
|
|
|
|
increase |
Positive |
|
22 |
Chlorpromazine |
|
|
|
|
|
decrease |
Positive |
|
22 |
Chlorpromazine |
|
|
|
|
|
increase |
Positive |
|
22 |
Chlorpromazine |
|
|
rat |
isolated liver mitochondria |
|
decrease |
Positive |
|
23 |
Haloperidol |
|
|
rat |
isolated liver mitochondria |
|
decrease |
Positive |
|
23 |
Risperidone |
|
|
rat |
isolated liver mitochondria |
|
decrease |
Positive |
|
23 |
quetiapine |
|
|
rat |
isolated liver mitochondria |
|
decrease |
Positive |
|
23 |
2,4-dinitrophenol |
|
|
|
|
|
increase |
Positive |
|
24 |
2,4-dinitrophenol |
|
|
|
|
|
increase |
Positive |
|
24 |
2,4-dinitrophenol |
|
|
|
|
|
increase |
Positive |
|
24 |
2-Deoxy-D-glucose |
|
|
human |
SkBr3 breast cancer cells |
MTT assay |
decrease |
Positive |
|
25 |
Antimycin A |
|
|
|
|
|
decrease |
Positive |
|
26 |
FOX-988 |
|
|
|
|
|
decrease |
Positive |
|
28 |
Sdz-51641 |
|
|
|
|
|
decrease |
Positive |
|
28 |
Myxothiazol |
|
|
bovine |
heart mitochondria |
|
decrease |
Positive |
|
29 |
Papaverine |
|
|
|
|
|
decrease |
Positive |
|
30 |
Salicylic acid |
|
|
|
|
|
decrease |
Positive |
|
32 |
Thenoyltrifluoroacetone |
|
|
|
|
|
decrease |
Positive |
|
33 |
thiazolidinediones |
|
|
|
|
|
decrease |
Positive |
|
34 |
Acetaminophen |
|
|
|
|
|
decrease |
Positive |
|
35 |
Acetaminophen |
|
|
|
|
|
decrease |
Positive |
|
35 |
Acetylsalicylic acid |
|
|
|
|
|
decrease |
Positive |
|
35 |
Acetylsalicylic acid |
|
|
|
|
|
decrease |
Positive |
|
35 |
Clotrimazole |
|
|
|
|
|
decrease |
Positive |
|
35 |
Flutamide |
|
|
|
|
|
decrease |
Positive |
|
35 |
Ketoconazole |
|
|
|
|
|
decrease |
Positive |
|
35 |
mefloquine |
|
|
|
|
|
decrease |
Positive |
|
35 |
Metformin |
|
|
|
|
|
decrease |
Positive |
|
35 |
Nefazodone |
|
|
|
|
|
decrease |
Positive |
|
35 |
Nitrofurantoin |
|
|
|
|
|
decrease |
Positive |
|
35 |
Paraquat |
|
|
|
|
|
decrease |
Positive |
|
35 |
paroxetine |
|
|
|
|
|
decrease |
Positive |
|
35 |
paroxetine |
|
|
|
|
|
decrease |
Positive |
|
35 |
paroxetine |
|
|
|
|
|
decrease |
Positive |
|
35 |
paroxetine |
|
|
|
|
|
decrease |
Positive |
|
35 |
Perhexiline |
|
|
|
|
|
decrease |
Positive |
|
35 |
Phenformin |
|
|
|
|
|
decrease |
Positive |
|
35 |
Pioglitazone |
|
|
|
|
|
decrease |
Positive |
|
35 |
Pioglitazone |
|
|
|
|
|
decrease |
Positive |
|
35 |
promethazine |
|
|
|
|
|
decrease |
Positive |
|
35 |
Rosiglitazone |
|
|
|
|
|
decrease |
Positive |
|
35 |
Rotenone |
|
|
|
|
|
decrease |
Positive |
|
35 |
Tamoxifen |
|
|
|
|
|
decrease |
Positive |
|
35 |
Tamoxifen |
|
|
|
|
|
decrease |
Positive |
|
35 |
Tamoxifen |
|
|
|
|
|
decrease |
Positive |
|
35 |
Tamoxifen |
|
|
|
|
|
decrease |
Positive |
|
35 |
Troglitazone |
|
|
|
|
|
decrease |
Positive |
|
35 |
2-Deoxy-D-glucose |
|
|
|
|
|
decrease |
Positive |
|
35 |
Antimycin A |
|
|
|
|
|
decrease |
Positive |
|
35 |
Etomoxir |
|
|
|
|
|
decrease |
Positive |
|
35 |
Myxothiazol |
|
|
|
|
|
decrease |
Positive |
|
35 |
Oligomycin |
|
|
|
|
|
decrease |
Positive |
|
35 |
Salicylic acid |
|
|
|
|
|
decrease |
Positive |
|
35 |
Thenoyltrifluoroacetone |
|
|
|
|
|
decrease |
Positive |
|
35 |
thiazolidinediones |
|
|
|
|
|
decrease |
Positive |
|
35 |
alpidem |
|
|
|
|
|
decrease |
Positive |
|
36 |
Amiodarone |
|
|
|
|
|
decrease |
Positive |
|
36 |
benzbromarone |
|
|
|
|
|
decrease |
Positive |
|
37 |
Chlorpromazine |
|
|
|
|
|
decrease |
Positive |
|
7 |
clomipramine |
|
|
|
|
|
decrease |
Positive |
|
38 |
Diclofenac |
|
|
|
|
|
decrease |
Positive |
|
39 |
Flutamide |
|
|
|
|
|
decrease |
Positive |
|
41 |
Ketoconazole |
|
|
|
|
|
decrease |
Positive |
|
36 |
lovastatin |
|
|
|
|
|
decrease |
Positive |
|
36 |
Phenformin |
|
|
|
|
|
decrease |
Positive |
|
43 |
Rosiglitazone |
|
|
|
|
|
decrease |
Positive |
|
7 |
Simvastatin |
|
|
|
|
|
decrease |
Positive |
|
7 |
sitaxsentan |
|
|
|
|
|
decrease |
Positive |
|
44 |
Tamoxifen |
|
|
|
|
|
decrease |
Positive |
|
46 |
Troglitazone |
|
|
|
|
|
decrease |
Positive |
|
7 |
Doxorubicin |
|
|
|
|
|
decrease |
Positive |
|
36 |
imipramine |
|
|
|
|
|
decrease |
Positive |
|
36 |
sertraline |
|
|
|
|
|
decrease |
Positive |
|
48 |
zoniporide |
|
|
|
|
|
decrease |
Positive |
|
50 |
pentamidine |
|
|
|
|
|
decrease |
Positive |
|
51 |
ritonavir |
|
|
|
|
|
decrease |
Positive |
|
36 |
Tenofovir |
|
|
|
|
|
decrease |
Positive |
|
52 |
Polymyxin B |
|
|
rat |
isolated liver mitochondria |
measurements of mitochondrial respiration; RST inhibition assay, RST uncoupling assay; IC 50ratio of glucose/galactose assay |
decrease |
Positive |
|
53 |
beclomethasone |
|
|
rat |
isolated liver mitochondria |
measurements of mitochondrial respiration; RST inhibition assay, RST uncoupling assay; IC 50ratio of glucose/galactose assay |
decrease |
Positive |
|
53 |
bicalutamide |
|
|
rat |
isolated liver mitochondria |
measurements of mitochondrial respiration; RST inhibition assay, RST uncoupling assay; IC 50ratio of glucose/galactose assay |
decrease |
Positive |
|
53 |
danazol |
|
|
rat |
isolated liver mitochondria |
measurements of mitochondrial respiration; RST inhibition assay, RST uncoupling assay; IC 50ratio of glucose/galactose assay |
decrease |
Positive |
|
53 |
ethynodiol diacetate |
|
|
rat |
isolated liver mitochondria |
measurements of mitochondrial respiration; RST inhibition assay, RST uncoupling assay; IC 50ratio of glucose/galactose assay |
decrease |
Positive |
|
53 |
retinoic acid |
|
|
rat |
isolated liver mitochondria |
measurements of mitochondrial respiration; RST inhibition assay, RST uncoupling assay; IC 50ratio of glucose/galactose assay |
decrease |
Positive |
|
53 |
aripiprazole |
|
|
rat |
isolated liver mitochondria |
measurements of mitochondrial respiration; RST inhibition assay, RST uncoupling assay; IC 50ratio of glucose/galactose assay |
decrease |
Positive |
|
53 |
axitinib |
|
|
rat |
isolated liver mitochondria |
measurements of mitochondrial respiration; RST inhibition assay, RST uncoupling assay; IC 50ratio of glucose/galactose assay |
decrease |
Positive |
|
53 |
clofilium |
|
|
rat |
isolated liver mitochondria |
measurements of mitochondrial respiration; RST inhibition assay, RST uncoupling assay; IC 50ratio of glucose/galactose assay |
decrease |
Positive |
|
53 |
tenidap |
|
|
rat |
isolated liver mitochondria |
measurements of mitochondrial respiration; RST inhibition assay, RST uncoupling assay; IC 50ratio of glucose/galactose assay |
decrease |
Positive |
|
53 |
darifenacin |
|
|
rat |
isolated liver mitochondria |
measurements of mitochondrial respiration; RST inhibition assay, RST uncoupling assay; IC 50ratio of glucose/galactose assay |
decrease |
Positive |
|
53 |
pimozide |
|
|
rat |
isolated liver mitochondria |
measurements of mitochondrial respiration; RST inhibition assay, RST uncoupling assay; IC 50ratio of glucose/galactose assay |
decrease |
Positive |
|
53 |
amineptine |
|
|
|
|
|
decrease |
Positive |
|
54 |
Gemfibrozil |
|
|
|
isolated mitochondria |
|
decrease |
Positive |
|
7 |
pirprofen |
|
|
|
|
|
decrease |
Positive |
|
59 |
Amitriptyline |
|
|
pig |
brain mitochondria |
|
decrease |
Positive |
|
60 |
Bupivacaine |
|
|
|
|
|
decrease |
Positive |
|
61 |
citalopram |
|
|
pig |
brain mitochondria |
|
decrease |
Positive |
|
62 |
citalopram |
|
|
pig |
brain mitochondria |
|
decrease |
Positive |
|
62 |
citalopram |
|
|
pig |
brain mitochondria |
|
decrease |
Positive |
|
62 |
Haloperidol |
|
|
|
|
|
decrease |
Positive |
|
23 |
propranolol |
|
|
pig |
brain mitochondria |
|
decrease |
Positive |
|
60 |
Indomethacin |
|
|
rat |
isolated liver mitochondria |
|
decrease |
Positive |
|
65 |
ochratoxin a |
|
|
rat |
isolated liver mitochondria |
|
decrease |
Positive |
|
66 |
tacrolimus |
|
|
rat |
isolated kidney mitochondria |
|
decrease |
Positive |
|
68 |
Piericidin A |
|
|
|
|
|
affect |
Positive |
|
53 |
rolliniastatin-2 |
|
|
|
|
|
affect |
Positive |
|
53 |
Idebenone |
|
|
|
|
|
affect |
Positive |
|
53 |
Rotenone |
|
|
|
|
|
affect |
Positive |
|
53 |
piericidin a |
|
|
|
|
|
affect |
Positive |
|
53 |
piericidin b |
|
|
|
|
|
affect |
Positive |
|
53 |
aureothin |
|
|
|
|
|
affect |
Positive |
|
53 |
amytal |
|
|
|
|
|
affect |
Positive |
|
53 |
4-alkyl-acridones |
|
|
|
|
|
affect |
Positive |
|
53 |
4′-alkyl-mpp+ analoguesc |
|
|
|
|
|
affect |
Positive |
|
53 |
phenoxan |
|
|
|
|
|
affect |
Positive |
|
53 |
quinol products |
|
|
|
|
|
affect |
Positive |
|
53 |
reduced q-2b |
|
|
|
|
|
affect |
Positive |
|
53 |
Myxothiazol |
|
|
|
|
|
affect |
Positive |
|
53 |
stigmatellin |
|
|
|
|
|
affect |
Positive |
|
53 |
TDS |
|
|
|
|
|
affect |
Positive |
|
53 |
2M-TIO |
|
|
|
|
|
affect |
Positive |
|
53 |
meperidine |
|
|
|
|
|
affect |
Positive |
|
53 |
para-nonylphenol |
|
|
|
|
|
affect |
Positive |
|
53 |
Diphenyleneiodonium chloride |
|
|
|
|
|
affect |
Positive |
|
69 |
ethoxyformic anhydride |
|
|
|
|
|
affect |
Positive |
|
70 |
ethoxyformic anhydride |
|
|
|
|
|
decrease |
Positive |
|
70 |
ethoxyformic anhydride |
|
|
|
|
|
decrease |
Positive |
|
70 |
flutolanil |
|
|
|
|
|
affect |
Positive |
|
71 |
atpenin a5 |
|
|
|
|
|
affect |
Positive |
|
71 |
Carboxin |
|
|
|
|
|
affect |
Positive |
|
71 |
penthiopyrad |
|
|
|
|
|
affect |
Positive |
|
71 |
boscalid |
|
|
|
|
|
affect |
Positive |
|
71 |
fluopyram |
|
|
|
|
|
affect |
Positive |
|
71 |
dinitrophenol-17 |
|
|
|
|
|
affect |
Positive |
|
71 |
atpenin a5 |
|
|
|
|
|
affect |
Positive |
|
72 |
thiophene carboxamides |
|
|
|
|
|
affect |
Positive |
|
73 |
HQNO |
|
|
|
|
|
affect |
Positive |
|
74 |
Polymyxin B |
1.6 μg/ml |
|
Mycobacterium smegmatis |
membrane-bound dehydrogenases |
|
decrease |
Positive |
IC50 |
76 |
nanaomycin a |
31 μg/ml |
|
Mycobacterium smegmatis |
membrane-bound dehydrogenases |
|
decrease |
Positive |
IC50 |
76 |
Polymyxin B |
1.6 μg/ml |
|
Mycobacterium smegmatis |
membrane-bound dehydrogenases |
|
affect |
Positive |
IC50 |
76 |
nanaomycin a |
31 μg/ml |
|
Mycobacterium smegmatis |
membrane-bound dehydrogenases |
|
affect |
Positive |
IC50 |
76 |
siccanin |
|
|
P. aeruginosa |
PAO1 cells |
|
affect |
Positive |
|
76 |
cyenopyrafen |
|
|
|
|
|
affect |
Positive |
|
77 |
pyflubumide |
|
|
|
|
|
affect |
Positive |
|
77 |
3-Nitropropionate |
|
|
|
|
|
affect |
Positive |
|
78 |
Malonate |
|
|
|
|
|
affect |
Positive |
|
79 |
oxaloacetate |
|
|
|
|
|
affect |
Positive |
|
79 |
malate |
|
|
|
|
|
affect |
Positive |
|
79 |
citrate |
|
|
|
|
|
affect |
Positive |
|
79 |
fumarate |
|
|
|
|
|
affect |
Positive |
|
79 |
british anti-lewisite |
|
|
|
|
|
affect |
Positive |
|
80 |
Myxothiazol |
|
|
|
|
|
affect |
Positive |
|
81 |
moas |
|
|
|
|
|
affect |
Positive |
|
82 |
azoxystrobin |
|
|
|
|
|
affect |
Positive |
|
83 |
oudemansin a |
|
|
|
|
|
affect |
Positive |
|
84 |
strobilurin a |
|
|
|
|
|
affect |
Positive |
|
84 |
cpmb-oxime |
|
|
|
|
|
affect |
Positive |
|
84 |
azoxystrobin |
100 mM |
incubated overnight |
bovine |
isolated heart mitochondria |
Measurements of redox potentials of the ISP |
affect |
Positive |
|
83 |
famoxadone |
100 mM |
incubated overnight |
bovine |
isolated heart mitochondria |
Measurements of redox potentials of the ISP |
affect |
Positive |
|
83 |
stigmatellin |
100 mM |
incubated overnight |
bovine |
isolated heart mitochondria |
Measurements of redox potentials of the ISP |
affect |
Positive |
|
83 |
uhdbt |
100 mM |
incubated overnight |
bovine |
isolated heart mitochondria |
Measurements of redox potentials of the ISP |
affect |
Positive |
|
83 |
hhdbt uhnq |
100 mM |
incubated overnight |
bovine |
isolated heart mitochondria |
Measurements of redox potentials of the ISP |
affect |
Positive |
|
83 |
dibromothymoquinone |
100 mM |
incubated overnight |
bovine |
isolated heart mitochondria |
Measurements of redox potentials of the ISP |
affect |
Positive |
|
83 |
Antimycin A |
|
|
bovine |
isolated heart mitochondria cytochrome bc1 complex |
|
affect |
Positive |
|
166 |
diuron |
|
|
|
|
|
affect |
Positive |
|
83 |
NQNO |
|
|
bovine |
isolated heart mitochondria cytochrome bc1 complex |
|
affect |
Positive |
|
166 |
NQNO |
|
|
bovine |
isolated heart mitochondria cytochrome bc1 complex |
|
affect |
Positive |
|
166 |
Carbon Monoxide |
|
|
|
|
|
affect |
Positive |
|
167 |
nitric oxide |
|
|
|
|
|
affect |
Positive |
|
167 |
Cyanide |
|
|
|
|
|
affect |
Positive |
|
167 |
azides |
|
|
|
|
|
affect |
Positive |
|
167 |
sulfide |
|
|
|
|
|
affect |
Positive |
|
167 |
formate |
|
|
|
|
|
affect |
Positive |
|
167 |
ethylxanthate |
|
|
|
|
|
affect |
Positive |
|
167 |
bisulfate |
|
|
|
|
|
affect |
Positive |
|
167 |
semicarbazide |
|
|
|
|
|
affect |
Positive |
|
167 |
salicyaldoxime |
|
|
|
|
|
affect |
Positive |
|
167 |
ethylxanthate |
|
|
|
|
|
decrease |
Positive |
|
167 |
bisulfate |
|
|
|
|
|
decrease |
Positive |
|
167 |
semicarbazide |
|
|
|
|
|
decrease |
Positive |
|
167 |
salicyaldoxime |
|
|
|
|
|
decrease |
Positive |
|
167 |
adda 5 |
|
|
human |
U251 mitochondria |
CcO activity assay |
affect |
Positive |
|
168 |
tetrathiomolybdate |
30 μM |
48 hour |
human |
ECC-1 |
|
affect |
Positive |
|
169 |
tetrathiomolybdate |
30 μM |
48 hour |
human |
IGROV-1 |
|
affect |
Positive |
|
169 |
Oligomycin |
152 μg inhibitor/mg protein |
|
E. coli |
membrane vesicle, pH gradient formation |
|
affect |
Positive |
|
170 |
Oligomycin |
7.1 μg inhibitor/mg protein |
|
C. asciculate |
SMP-ATPase |
|
affect |
Positive |
IC50 |
170 |
Oligomycin |
2.0-3.0 μg inhibitor/mg protein |
|
S. cerevisiae |
SMP-ATPase |
|
affect |
Positive |
IC50 |
170 |
Oligomycin |
0.3 μM |
|
human NCI-60 cell lines |
F0F1-ATPase |
|
affect |
Positive |
IC50 |
170 |
Oligomycin |
15 ng inhibitor/mg protein |
|
N. crassa |
SMP-ATPase |
|
affect |
Positive |
Ki |
170 |
Oligomycin |
0.21 μM |
|
bovine |
heart MF0F1-ATPase |
|
affect |
Positive |
Ki |
170 |
Oligomycin |
0.4 μg inhibitor/mg protein |
|
bovine |
heart SMP-ATPase |
|
affect |
Positive |
95% inhibition |
170 |
Oligomycin |
0.5 μg/ml |
|
rat |
liver SMP-ATPase |
|
affect |
Positive |
75% inhibition |
170 |
ossamycin |
46 μg of inhibitor/mg protein |
|
E. coli |
pH gradient formation by membrane vesicle |
|
affect |
Positive |
IC50 |
170 |
ossamycin |
8 μM |
|
human NCI-60 cell lines |
F0F1-ATPase |
|
affect |
Positive |
IC50 |
170 |
ossamycin |
1.3 μg of inhibitor/mg protein |
|
S. cerevisiae |
SMP-ATPase |
|
affect |
Positive |
IC50 |
170 |
venturicidin B |
|
|
|
|
|
affect |
Positive |
|
170 |
Bedaquiline |
|
|
|
|
|
affect |
Positive |
|
170 |
tributyltin chloride |
200 nM |
|
E. coli and |
F0F1-ATPase |
|
affect |
Positive |
|
170 |
tributyltin chloride |
200 nM |
|
I. tartaricus |
F0F1-ATPase |
|
affect |
Positive |
|
170 |
tributyltin chloride |
1 μM |
|
C. thermoaceticum |
membrane-bound F0F1-ATPase |
|
affect |
Positive |
47% inhibition |
170 |
tributyltin chloride |
5 μM |
|
C. thermoaceticum |
membrane-bound F0F1-ATPase |
|
affect |
Positive |
87% inhibition |
170 |
tributyltin chloride |
1 μM |
|
|
TF0F1-ATPase |
|
affect |
Positive |
80% inhibition |
170 |
NCCD |
0.65 nmol/mg protein |
|
bovine |
heart SMP-ATPase |
|
affect |
Positive |
IC50 |
170 |
NCCD |
1 nmol NCCD/mg protein |
|
bovine |
heart SMP-ATPase |
|
affect |
Positive |
85% inhibition |
170 |
substrate analogs |
|
|
|
|
|
affect |
Positive |
|
170 |
tentoxin |
∼0.6 mol/mol |
|
spinach |
CF1-ATPase |
|
affect |
Positive |
IC50 |
170 |
tentoxin |
50 nM |
|
spinach |
CF1(-ɛ)-ATPase |
|
affect |
Positive |
IC50 |
170 |
tentoxin |
0.4-0.6 μM |
|
lettuce |
chloroplasts, photophosphorylation |
|
affect |
Positive |
IC50 |
170 |
tentoxin |
10 nM |
|
spinach |
CF1(-ɛ)-ATPase |
|
affect |
Positive |
Ki |
170 |
tentoxin |
30-60 μM |
|
|
TF1-ATPase |
|
affect |
Positive |
Ki |
170 |
tentoxin |
8-10 nM |
|
spinach |
CF1(-ɛ)-ATPase |
|
affect |
Positive |
Kd |
170 |
efrapeptins |
|
|
|
|
|
affect |
Positive |
|
170 |
azide |
|
|
|
|
|
affect |
Positive |
|
170 |
resveratrol |
|
|
|
|
|
affect |
Positive |
|
170 |
N,N'-dicyclohexylcarbodiimide |
0.2 μg of inhibitor/mg protein |
|
S. cerevisiae |
SMP-ATPase |
|
affect |
Positive |
IC50 |
170 |
N,N'-dicyclohexylcarbodiimide |
1-5 μg of inhibitor/mg protein |
|
T. pyriformis |
SMP-ATPase |
|
affect |
Positive |
IC50 |
170 |
N,N'-dicyclohexylcarbodiimide |
200 μMa in less than 5 min and at ∼40 μMa in 30 min |
|
R. rubrum |
F1-ATPase |
|
affect |
Positive |
|
170 |
N,N'-dicyclohexylcarbodiimide |
1.9 μg/mg protein |
|
C. fasciculata |
SMP-ATPase |
|
affect |
Positive |
IC50 |
170 |
N,N'-dicyclohexylcarbodiimide |
1 mol DCCD/mol F1 |
|
|
EF1-ATPase |
|
affect |
Positive |
95% inhibition |
170 |
N,N'-dicyclohexylcarbodiimide |
30 μM |
|
|
membrane-bound EF0F1-ATPase |
|
affect |
Positive |
maximal 70-80% inhibition |
170 |
N,N'-dicyclohexylcarbodiimide |
5 μM |
|
C. thermoaceticum |
membrane-bound F0F1-ATPase |
|
affect |
Positive |
47% inhibition |
170 |
N,N'-dicyclohexylcarbodiimide |
2 mol inhibitor bound/mol F1 |
|
bovine |
heart MF1-ATPase |
|
affect |
Positive |
97% inhibition |
170 |
N,N'-dicyclohexylcarbodiimide |
1 mol inhibitor/mol F0 |
|
bovine |
heart SMP-ATPase |
|
affect |
Positive |
maximal inhibition |
170 |
N,N'-dicyclohexylcarbodiimide |
2 mol inhibitor/mol F0 |
|
bovine |
heart H+-translocation |
|
affect |
Positive |
maximal inhibition |
170 |
N,N'-dicyclohexylcarbodiimide |
1 mol inhibitor/mol F0 |
|
E. coli |
membrane H+-translocation |
|
affect |
Positive |
maximal inhibition |
170 |
N,N'-dicyclohexylcarbodiimide |
|
|
|
|
|
affect |
Positive |
|
170 |
woodward's reagent k |
|
|
|
|
|
affect |
Positive |
|
170 |
woodward's reagent k |
|
|
|
|
|
affect |
Positive |
|
170 |
Melittin |
5μM and 16μM |
|
bovine |
bovine heart MF1-ATPase |
|
|
Positive |
IC50 |
170 |
IF1 |
0.25 μM |
|
bovine |
bovine heart MF1-ATPase |
|
|
Positive |
IC50 |
170 |
IF1 |
1.2 μM |
|
bovine |
heart MF1-ATPase |
|
|
Positive |
IC50 |
170 |
IF1 |
0.84 μM |
|
bovine |
heart MF1-ATPase |
|
|
Positive |
IC50 |
170 |
IF1 |
300 μg/mg protein (T. pyriformis SMP-ATPase) ; |
|
|
|
|
|
Positive |
IC50 |
170 |
IF1 |
34 μg/mg protein |
|
C. asciculate |
SMP-ATPase |
|
|
Positive |
IC50 |
170 |
IF1 |
0.24 μM |
|
rat |
liver MF1-ATPase |
|
|
Positive |
Ki |
170 |
Angiostatin |
|
|
|
|
|
|
Positive |
|
170 |
Enterostatin |
|
|
|
|
|
|
Positive |
|
170 |
ethyldimethylaminopropyl carbodiimide |
13 mol of EDC/mol F1 (EF1-ATPase) |
|
|
|
|
|
Positive |
95% inhibition |
170 |
1,5-difluoro-2,4-dinitrobenzene |
|
|
|
|
|
|
Positive |
|
170 |
NBD-Cl |
|
|
|
|
|
|
Positive |
|
170 |
NBD-Cl |
|
|
|
|
|
|
Positive |
|
170 |
N-ethylmaleimide |
20 nmoles/mg protein |
|
bovine |
heart mitochondria and submitochondrial particles. |
Determination of the energized accumulation of Pi and the binding of ADP; Assay of energized translocation of calcium and Pi |
affect |
Positive |
|
228 |
Hypoglycin A |
|
|
|
|
|
|
Positive |
|
232 |
4-Pentenoic acid |
|
|
|
|
|
|
Positive |
|
232 |
2-bromooctanoic acid |
|
|
|
|
|
|
Positive |
|
232 |
2-tetradecylglycidic acid |
|
|
|
|
|
|
Positive |
|
232 |
2-bromopalmitic acid |
|
|
|
|
|
|
Positive |
|
232 |
Palmitoylcarnitine |
|
|
|
|
|
|
Positive |
|
232 |
cyclophilin D |
|
|
|
|
|
affect |
Positive |
|
171 |
triclosan |
0.5 µM |
|
zebrafish |
|
XFe24 Extracellular Flux Analyzer |
decrease |
Positive |
|
85 |
triclosan |
0.5 µM |
|
zebrafish |
|
XFe24 Extracellular Flux Analyzer |
decrease |
Positive |
|
85 |
triclosan |
0.5 µM |
|
zebrafish |
|
XFe24 Extracellular Flux Analyzer |
decrease |
Positive |
|
85 |
Benzo(A)Pyrene |
100 µg/l |
|
zebrafish |
|
XFe24 Extracellular Flux Analyzer |
decrease |
Positive |
|
85 |
Benzo(A)Pyrene |
1000 µg/l |
|
zebrafish |
|
XFe24 Extracellular Flux Analyzer |
decrease |
Positive |
|
85 |
phenanthrene |
500 µg/l |
|
zebrafish |
|
XFe24 Extracellular Flux Analyzer |
decrease |
Positive |
|
85 |
phenanthrene |
100 µg/l |
|
zebrafish |
|
XFe24 Extracellular Flux Analyzer |
decrease |
Positive |
|
85 |
phenanthrene |
500 µg/l |
|
zebrafish |
|
XFe24 Extracellular Flux Analyzer |
increase |
Positive |
|
85 |
fluoranthene |
100 µg/l |
|
zebrafish |
|
XFe24 Extracellular Flux Analyzer |
decrease |
Positive |
|
85 |
fluoranthene |
100 µg/l |
|
zebrafish |
|
XFe24 Extracellular Flux Analyzer |
decrease |
Positive |
|
85 |
fluoranthene |
100 µg/l |
|
zebrafish |
|
XFe24 Extracellular Flux Analyzer |
decrease |
Positive |
|
85 |
fluoranthene |
100 µg/l |
|
zebrafish |
|
XFe24 Extracellular Flux Analyzer |
increase |
Positive |
|
85 |
Phenanthrenequinone |
2 µM |
|
zebrafish |
|
XFe24 Extracellular Flux Analyzer |
decrease |
Positive |
|
86 |
benz(a)anthracene-7,12-dione |
5 µM |
|
zebrafish |
|
XFe24 Extracellular Flux Analyzer |
decrease |
Positive |
|
86 |
9,10-anthraquinone |
20 µM |
|
zebrafish |
|
XFe24 Extracellular Flux Analyzer |
decrease |
Positive |
|
86 |
1,9-benz-10-anthrone |
10 µM |
|
zebrafish |
|
XFe24 Extracellular Flux Analyzer |
decrease |
Positive |
|
86 |
Phenanthrenequinone |
2 µM |
|
zebrafish |
|
XFe24 Extracellular Flux Analyzer |
decrease |
Positive |
|
86 |
xanthone |
20 µM |
|
zebrafish |
|
XFe24 Extracellular Flux Analyzer |
decrease |
Positive |
|
86 |
benz(a)anthracene-7,12-dione |
5 µM |
|
zebrafish |
|
XFe24 Extracellular Flux Analyzer |
decrease |
Positive |
|
86 |
1,9-benz-10-anthrone |
10 µM |
|
zebrafish |
|
XFe24 Extracellular Flux Analyzer |
decrease |
Positive |
|
86 |
9,10-anthraquinone |
20 µM |
|
zebrafish |
|
XFe24 Extracellular Flux Analyzer |
decrease |
Positive |
|
86 |
1,9-benz-10-anthrone |
10 µM |
|
zebrafish |
|
XFe24 Extracellular Flux Analyzer |
decrease |
Positive |
|
86 |
xanthone |
20 µM |
|
zebrafish |
|
XFe24 Extracellular Flux Analyzer |
decrease |
Positive |
|
86 |
triclosan |
30 μM |
|
zebrafish |
|
XFe24 Extracellular Flux Analyzer |
decrease |
Positive |
|
89 |
triclosan |
30 μM |
|
zebrafish |
|
XFe24 Extracellular Flux Analyzer |
decrease |
Positive |
|
89 |
triclosan |
30 μM |
|
zebrafish |
|
XFe24 Extracellular Flux Analyzer |
increase |
Positive |
|
89 |
2,4-dinitrophenol |
0.5 μM / 6 hpf |
|
zebrafish |
|
XFe24 Extracellular Flux Analyzer |
increase |
Positive |
|
90 |
2,4-dinitrophenol |
0.5 μM / 48 hpf |
|
zebrafish |
|
XFe24 Extracellular Flux Analyzer |
decrease |
Positive |
|
90 |
2,4-dinitrophenol |
0.5 μM / 24 hpf |
|
zebrafish |
|
XFe24 Extracellular Flux Analyzer |
affect |
Positive |
|
90 |
2,4-dinitrophenol |
0.5 μM / 48 hpf |
|
zebrafish |
|
XFe24 Extracellular Flux Analyzer |
decrease |
Positive |
|
90 |
2,4-dinitrophenol |
0.5 μM / 24 hpf |
|
zebrafish |
|
XFe24 Extracellular Flux Analyzer |
decrease |
Positive |
|
90 |
2,4-dinitrophenol |
0.5 μM / 24 hpf |
|
zebrafish |
|
XFe24 Extracellular Flux Analyzer |
decrease |
Positive |
|
90 |
2,4-dinitrophenol |
0.5 μM / 24 hpf |
|
zebrafish |
|
XFe24 Extracellular Flux Analyzer |
increase |
Positive |
|
90 |
quercetin |
1 µg/l |
|
zebrafish |
|
XFe24 Extracellular Flux Analyzer |
decrease |
Positive |
|
91 |
quercetin |
1 µg/l |
|
zebrafish |
|
XFe24 Extracellular Flux Analyzer |
decrease |
Positive |
|
91 |
quercetin |
10 µg/l |
|
zebrafish |
|
XFe24 Extracellular Flux Analyzer |
decrease |
Positive |
|
91 |
diquat |
100 μM |
|
zebrafish |
|
XFe24 Extracellular Flux Analyzer |
decrease |
Positive |
|
92 |
diquat |
100 μM |
|
zebrafish |
|
XFe24 Extracellular Flux Analyzer |
decrease |
Positive |
|
92 |
Rotenone |
0.07 nmol/mg |
|
bovine |
mitochondria |
NADH–Q |
decrease |
Positive |
IC50 |
94 |
Rotenone |
0.04 nmol/mg |
|
bovine |
mitochondria |
NADH–O2 |
decrease |
Positive |
IC50 |
94 |
Deguelin |
4.2 nmol/mg |
|
bovine |
mitochondria |
NADH–Q |
decrease |
Positive |
IC50 |
95 |
Piericidin A |
0.06 nmol/mg |
|
bovine |
mitochondria |
NADH–Q |
decrease |
Positive |
IC50 |
94 |
Piericidin A |
0.03 nmol/mg |
|
bovine |
mitochondria |
NADH:O2 |
decrease |
Positive |
IC50 |
94 |
Ubicidin-3 |
0.17 nmol/mg |
|
bovine |
mitochondria |
NADH:O2 |
decrease |
Positive |
IC50 |
96 |
Rolliniastatin-1 |
0.03 nmol/mg |
|
bovine |
mitochondria |
NADH–Q |
decrease |
Positive |
IC50 |
98 |
rolliniastatin-2 |
0.06 nmol/mg |
|
bovine |
mitochondria |
NADH–Q-1 |
decrease |
Positive |
IC50 |
98 |
Otivarin |
0.2 nmol/mg |
|
bovine |
mitochondria |
NADH–Q |
decrease |
Positive |
IC50 |
98 |
phenoxan |
0.04 nmol/mg |
|
bovine |
mitochondria |
NADH–Q |
decrease |
Positive |
IC50 |
94 |
Thiangazole |
0.04 nmol/mg |
|
bovine |
mitochondria |
NADH–Q |
decrease |
Positive |
IC50 |
94 |
myxalamid pi |
15 nmol/mg |
|
bovine |
mitochondria |
NADH–Q |
decrease |
Positive |
IC50 |
94 |
phenalamid a2 |
0.6 nmol/mg |
|
bovine |
mitochondria |
NADH–Q |
decrease |
Positive |
IC50 |
94 |
Aurachin a |
8.0 nmol/mg |
|
bovine |
mitochondria |
NADH–Q |
decrease |
Positive |
IC50 |
94 |
Myxothiazol |
20 nmol/mg |
|
bovine |
mitochondria |
NADH–Q |
decrease |
Positive |
IC50 |
99 |
stigmatellin |
100 nmol/mg |
|
bovine |
mitochondria |
NADH–Q |
decrease |
Positive |
IC50 |
99 |
TDS |
40 nmol/mg |
|
bovine |
mitochondria |
NADH–Q |
decrease |
Positive |
IC50 |
99 |
aureothin |
0.3 nmol/mg |
|
bovine |
mitochondria |
NADH–Q |
decrease |
Positive |
IC50 |
94 |
Cochlioquinone b |
83 nmol/mg |
|
bovine |
mitochondria |
NADH:O2 |
decrease |
Positive |
IC50 |
100 |
strobilurin a |
>100 nmol/mg |
|
bovine |
mitochondria |
NADH–Q |
decrease |
Positive |
IC50 |
99 |
pterulone |
36 μM |
|
bovine |
mitochondria |
NADH:O2 |
decrease |
Positive |
IC50 |
101 |
Capsaicin |
20–30 μM |
|
bovine |
mitochondria |
NADH–Q |
decrease |
Positive |
IC50 |
102 |
Capsaicin |
20–30 μM |
|
bovine |
mitochondria |
NADH:O2 |
decrease |
Positive |
IC50 |
102 |
Rhein |
30 μM |
|
bovine |
mitochondria |
NADH:O2 |
decrease |
Positive |
IC50 |
104 |
Papaverine |
5 μM |
|
bovine |
mitochondria |
NADH–Q-1 |
decrease |
Positive |
IC50 |
30 |
Ubiquinone-2 |
2 μM |
|
bovine |
mitochondria |
NADH–Q-1 |
decrease |
Positive |
IC50 |
106 |
Ubiquinone-3 |
40 μM |
|
bovine |
mitochondria |
NADH–Q |
decrease |
Positive |
IC50 |
107 |
Idebenone |
0.4 μM |
|
|
|
NADH–Q |
decrease |
Positive |
IC50 |
106 |
Pyridaben |
2.4 nM |
|
|
|
NADH–Q-1 |
decrease |
Positive |
IC50 |
108 |
Fenpyroximate |
4.6 nM |
|
|
|
NADH–Q-1 |
decrease |
Positive |
IC50 |
108 |
Fenpyroximate |
18 nM |
|
|
|
NADH–Q |
decrease |
Positive |
IC50 |
103 |
Tebufenpyrad |
6 nM |
|
|
|
NADH–Q-1 |
decrease |
Positive |
IC50 |
108 |
fenazaquin |
20 nM |
|
|
|
NADH–Q-1 |
decrease |
Positive |
IC50 |
109 |
Benzimidazole |
3 nM |
|
|
|
NADH–Q |
decrease |
Positive |
IC50 |
94 |
cyhalothrin |
0.6 μM |
|
|
|
NADH–DQ |
decrease |
Positive |
IC50 |
110 |
6-chloro-benzothiadiazole |
0.1 mM |
|
|
|
NADH:O2 |
decrease |
Positive |
IC50 |
111 |
2M-TIO |
40 μM |
|
|
|
NADH–Q-1 |
decrease |
Positive |
IC50 |
112 |
amytal |
0.2 mM |
|
|
|
NADH–Q-1 |
decrease |
Positive |
IC50 |
112 |
meperidine |
0.1 mM |
|
|
|
NADH–Q-1 |
decrease |
Positive |
IC50 |
108 |
MPP+ |
0.3 mM |
|
|
|
NADH:O2 |
decrease |
Positive |
IC50 |
114 |
MPP+ |
2–4 mM |
|
|
|
NADH–Q |
decrease |
Positive |
IC50 |
115 |
4'-decyl-mpp+ |
1.7 μM |
|
|
|
NADH:O2 |
decrease |
Positive |
IC50 |
115 |
MQ18 |
0.2 μM |
|
|
|
NADH–Q-1 |
decrease |
Positive |
IC50 |
116 |
2-methylharmine |
0.18 mM |
|
|
|
NADH:O2 |
decrease |
Positive |
IC50 |
117 |
TIQ |
2 mM |
|
|
|
NADH:O2 |
decrease |
Positive |
IC50 |
118 |
Haloperidol |
3 μM |
|
|
|
NADH–Q-1 |
decrease |
Positive |
IC50 |
119 |
HPP+ |
15 μM |
|
|
|
NADH–Q-1 |
decrease |
Positive |
IC50 |
119 |
Dequalinium Chloride |
11 μM |
|
|
|
NADH:O2 |
decrease |
Positive |
IC50 |
120 |
Cinnarizine |
5–10 μM |
|
|
|
NADH–Q-1 |
decrease |
Positive |
IC50 |
121 |
para-nonylphenol |
20 μM |
|
|
|
NADH–Q |
decrease |
Positive |
IC50 |
108 |
Catechol |
0.4 mM |
|
|
|
NADH–Q |
decrease |
Positive |
IC50 |
108 |
CCCP |
85 μM |
|
|
|
NADH–Q-1 |
decrease |
Positive |
IC50 |
108 |
Erythrosin 5'-iodoacetamide |
20 nM |
|
|
|
NADH–O2 |
decrease |
Positive |
IC50 |
126 |
Safranine |
17 μM |
|
|
|
NADH–Q |
decrease |
Positive |
IC50 |
127 |
dioc5(3) |
1.5 μM |
|
|
|
NADH–Q |
decrease |
Positive |
IC50 |
127 |
dioc6(3) |
80 nM |
|
|
|
NADH–O2 |
decrease |
Positive |
IC50 |
126 |
Diphenyleneiodonium chloride |
0.23 μM |
|
|
|
NADH–Q-1c |
decrease |
Positive |
IC50 |
128 |
N,N'-dicyclohexylcarbodiimide |
0.1 mM |
|
|
|
NADH–Q-1 |
decrease |
Positive |
IC50 |
129 |
o-phenanthroline |
0.25 mM |
|
|
|
NADH–Q |
decrease |
Positive |
IC50 |
130 |
Leucinostatin |
11 μg/mg protein |
|
C. asciculate |
SMP-ATPase |
|
decrease |
Positive |
IC50 |
131 |
Leucinostatin |
2 μg inhibitor/ml |
|
spinach |
chloroplast |
|
decrease |
Positive |
IC50 |
132 |
Leucinostatin |
0.1-0.4 μg/mg protein |
|
rat |
isolated liver mitochondria |
|
decrease |
Positive |
|
133 |
efrapeptins |
0.56 mol/mol F1 |
|
bovine |
heart MF1-ATPase |
|
decrease |
Positive |
IC50 |
134 |
efrapeptins |
70 ng/ml |
|
C. asciculate |
MF1-ATPase |
|
decrease |
Positive |
IC50 |
135 |
efrapeptins |
0.3 μM |
|
human |
umbilical vein endothelial cell, nonmitochondrial ATP synthase |
|
decrease |
Positive |
IC50 |
136 |
efrapeptins |
0.5 μg/ml |
|
R. rubrum |
chromatophores |
|
decrease |
Positive |
IC50 |
137 |
efrapeptins |
0.05-0.5 μg of inhibitor/mg protein |
|
T. pyriformis |
SMP-ATPase |
|
decrease |
Positive |
IC50 |
138 |
efrapeptins |
21.5 μM |
|
|
EF1-ATPase |
|
decrease |
Positive |
ki |
139 |
efrapeptins |
10 nM |
|
bovine |
heart MF1-ATPase |
|
decrease |
Positive |
kd |
134 |
efrapeptins |
2.4 mol inhibitor/mol enzyme |
|
bovine |
heart SMP-ATPase |
|
decrease |
Positive |
complete inhibition |
134 |
resveratrol |
27.7 μM |
|
rat |
brain SMP, ATP synthesis |
|
decrease |
Positive |
|
140 |
resveratrol |
14 μM |
|
rat |
liver MF1-ATPase |
|
decrease |
Positive |
|
141 |
resveratrol |
19 μM |
|
rat |
brain M F0F1-ATPase |
|
decrease |
Positive |
|
140 |
resveratrol |
6.4 μM |
|
bovine |
bovine heart MF1-ATPase |
|
decrease |
Positive |
|
142 |
resveratrol |
2 μM |
|
human |
human umbilical vein endothelial cell, nonmitochondrial ATP synthase, ATP synthesis |
|
decrease |
Positive |
|
136 |
Diethylstilbestrol |
10 μM |
|
rat |
liver MF0F1-ATPase |
|
decrease |
Positive |
|
143 |
Diethylstilbestrol |
10-25 μM |
|
rat |
brain MF0F1-ATPase |
|
decrease |
Positive |
|
141 |
SITS |
∼1.3 μM |
|
V. parahaemolyticus |
F0F1-ATPase |
|
decrease |
Positive |
|
144 |
SITS |
25 μM |
|
V. parahaemolyticus |
F1-ATPase |
|
decrease |
Positive |
95% inhibition |
145 |
DIDS |
20.9 μM |
|
rat |
liver MF1ATPase |
|
decrease |
Positive |
|
146 |
quercetin |
5 kmol/mol |
|
bovine |
heart MF1-ATPase |
|
decrease |
Positive |
IC50 |
147 |
quercetin |
85 μM |
|
bovine |
heart MF1-ATPase |
|
decrease |
Positive |
IC50 |
148 |
quercetin |
180 μM |
|
bovine |
heart SMP-ATPase |
|
decrease |
Positive |
IC50 |
148 |
quercetin |
50 μM |
|
rat |
brain F0F1-ATPase |
|
decrease |
Positive |
IC50 |
140 |
quercetin |
3 μM |
|
rat |
liver F1-ATPase |
|
decrease |
Positive |
IC50 |
141 |
quercetin |
2 kmol/mola |
|
spinach |
CF1-ATPase |
|
decrease |
Positive |
|
147 |
quercetin |
2.6 μg/mg protein |
|
C. asciculate |
SMP-ATPase |
|
decrease |
Positive |
IC50 |
131 |
quercetin |
0.2 mM |
|
pig |
heart MF1-ATPase |
|
decrease |
Positive |
Ki |
149 |
quercetin |
27 μM |
|
bovine |
heart MF1-ATPase |
|
decrease |
Positive |
Kd |
147 |
quercetin |
5 μM |
|
C. thermoaceticum |
membrane-bound F0F1-ATPase |
|
decrease |
Positive |
46% inhibition |
150 |
kaempferol |
55 μM |
|
rat |
brain MF0F1-ATPase |
|
decrease |
Positive |
IC50 |
140 |
morin |
60 μM |
|
rat |
brain MF0F1-ATPase |
|
decrease |
Positive |
IC50 |
140 |
apigenin |
105 μM |
|
rat |
brain MF0F1-ATPase |
|
decrease |
Positive |
IC50 |
140 |
genistein |
55 μM |
|
rat |
brain MF0F1-ATPase |
|
decrease |
Positive |
IC50 |
140 |
genistein |
50 μM |
|
rat |
liver F1-ATPase |
|
decrease |
Positive |
10% inhibition |
141 |
Biochanin A |
65 μM |
|
rat |
brain MF0F1-ATPase |
|
decrease |
Positive |
IC50 |
140 |
Daidzein |
127 μM |
|
rat |
brain MF0F1-ATPase |
|
decrease |
Positive |
IC50 |
151 |
Oligomycin |
152 μg inhibitor/mg protein |
|
E. coli |
membrane vesicle |
|
decrease |
Positive |
IC50 |
152 |
Oligomycin |
7.1 μg inhibitor/mg protein |
|
C. asciculate |
SMP-ATPase |
|
decrease |
Positive |
IC50 |
131 |
Oligomycin |
2.0-3.0 μg inhibitor/mg protein |
|
S. cerevisiae |
SMP-ATPase |
|
decrease |
Positive |
IC50 |
153 |
Oligomycin |
0.3 μM |
|
human |
NCI-60 cell lines, F0F1-ATPase |
|
decrease |
Positive |
IC50 |
154 |
Oligomycin |
15 ng inhibitor/mg protein |
|
N. crassa |
SMP-ATPase |
|
decrease |
Positive |
Ki |
155 |
Oligomycin |
0.21 μM |
|
bovine |
heart MF0F1-ATPase |
|
decrease |
Positive |
Ki |
156 |
Oligomycin |
0.4 μg inhibitor/mg protein |
|
bovine |
heart SMP-ATPase |
|
decrease |
Positive |
95% inhibition |
157 |
Oligomycin |
0.5 μg/ml |
|
rat |
liver SMP-ATPase |
|
decrease |
Positive |
75% inhibition |
158 |
peliomycin |
4.5 μg inhibitor/mg protein |
|
S. cerevisiae |
SMP-ATPase |
|
decrease |
Positive |
IC50 |
153 |
venturicidin B |
9 μg inhibitor/mg protein |
|
E. coli |
membrane vesicle |
|
decrease |
Positive |
IC50 |
152 |
venturicidin B |
11 μg inhibitor/mg protein |
|
E. coli |
membrane-bound ATPase |
|
decrease |
Positive |
IC50 |
152 |
venturicidin B |
0.13 μg inhibitor/mg protein |
|
|
|
|
decrease |
Positive |
IC50 |
153 |
venturicidin B |
0.06-0.18 (A and B) and 11.0 (X) μg inhibitor/mg protein |
|
S. cerevisiae |
SMP-ATPase |
|
decrease |
Positive |
IC50 |
159 |
venturicidin B |
5-11 μg inhibitor/mg protein |
|
T. pyriformis |
|
|
decrease |
Positive |
IC50 |
138 |
venturicidin B |
3.0 μg/mg protein |
|
C. asciculate |
SMP-ATPase |
|
decrease |
Positive |
IC50 |
131 |
venturicidin B |
0.5 μM |
|
spinach |
thylakoids |
|
decrease |
Positive |
IC50 |
160 |
venturicidin B |
0.5 μM |
|
spinach |
thylakoids, ATPase |
|
decrease |
Positive |
IC50 |
160 |
ossamycin |
1.3 μg of inhibitor/mg protein |
|
S. cerevisiae |
SMP-ATPase |
|
decrease |
Positive |
IC50 |
153 |
ossamycin |
46 μg of inhibitor/mg protein |
|
E. coli |
membrane vesicle |
|
decrease |
Positive |
IC50 |
152 |
ossamycin |
8 μM |
|
human |
NCI-60 cell lines, F0F1-ATPase |
|
decrease |
Positive |
IC50 |
154 |
apoptolidin |
4-5 μM |
|
S. cerevisiae |
membrane-bound F0F1-ATPase |
|
decrease |
Positive |
Ki |
161 |
apoptolidin |
18 μM |
|
human |
NCI-60 cell lines, F0F1-ATPase |
|
decrease |
Positive |
IC50 |
154 |
cytovaricin |
1 μM |
|
human |
NCI-60 cell lines, F0F1-ATPase |
|
decrease |
Positive |
IC50 |
154 |
cytovaricin |
0.4 μM |
|
S. cerevisiae |
membrane-bound F0F1-ATPase |
|
decrease |
Positive |
Ki |
161 |
ossamycin |
0.8 μM |
|
|
60 human cancer cell lines of the National Cancer Institute |
|
decrease |
Positive |
mean |
184 |
1h-benzimidazol-5-amine-2-4-aminophenyl |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
2-(Dimethylamino)-1,3-benzothiazol-6-ol |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
4-[(7-Nitro-2,1,3-benzoxadiazol-4-yl)amino]phenol |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
7,8-Dihydroxy-4-methylcoumarin |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
4-Amino-2-(5-ethyl-benzooxazol-2-yl)-phenol |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
(4-Methoxyphenyl)-[2-(p-anisidino)ethyl]amine |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
3,3'-Diamino-4,4'-dihydroxydiphenyl Sulfone |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
2-(4-Hydroxy-1H-indol-3-yl)acetamide |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
2,5-Bis(2-phenylacetamido)terephthalic acid |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
2,6-Dimethyl-5,12-dihydroindolo[3,2-d][1,3]benzodiazepine;hydrochloride |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
N-(4-{[(4,6-Dimethyl-2-pyrimidinyl)amino]sulfonyl}phenyl)-2,4-dimethoxybenzamide |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
N'-(4-Methoxybenzyl)-N,N-dimethylbenzene-1,3-diamine |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
4-(1,2,3,4-Tetrahydro-benzo[a]phenanthridin-5-yl)-benzene-1,2-diol |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
N-Benzyl-4-methoxyaniline |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
Methyl 2-amino-4-ethyl-5-methylthiophene-3-carboxylate |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
N-(4-(4-Methyl-1-piperazinyl)phenyl)-9-acridinamine |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
4-Chloro-N-(2-hydroxyphenyl)benzenesulfonamide |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
N-(4-Hydroxyphenyl)furan-2-carboxamide |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
(Z)-2-Cyano-3-(3-ethoxy-4-hydroxyphenyl)prop-2-enamide |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
(3-Bromo-4-hydroxyphenyl)[(4-chlorophenyl)sulfonyl]amine |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
2-Chloro-6-methylindolo[1,2-c]quinazolin-12-amine |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
4-(2,3-Dihydro-1H-benzo[f]cyclopenta[c]quinolin-4-yl)benzene-1,2-diol |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
(5E)-5-(4-Hydroxybenzylidene)-2-mercapto-1,3-thiazol-4(5H)-one |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
8-Chloro-2,2-dimethyl-2,3-dihydro-1H-phenothiazin-4(10H)-one |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
2-[(3,4-Dimethylphenyl)sulfonyl]benzene-1,4-diol |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
4-([4-(1H-Benzimidazol-2-yl)phenyl]amino)-4-oxobutanoic acid |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
Ethyl 2-ethoxy-5-hydroxy-1H-indole-3-carboxylate |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
4-(1,2,3,4-Tetrahydrobenzo[a]phenanthridin-5-yl)benzene-1,3-diol |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
N-(Cyclohexylmethyl)-4-methoxyaniline |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
N-(Furan-2-ylmethyl)-1,3-benzodioxol-5-amine |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
5-Nitro-2-phenyl-1H-indole |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
8-Chloro-2,3-dihydro-1H-phenothiazin-4(10H)-one |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
N-(4-Bromophenyl)-4,5,6,7-tetrahydro-1,3-benzothiazol-2-amine |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
2-[2-(2-Aminophenyl)vinyl]-5,7-dimethylquinolin-8-ol |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
4,6-Dimethyl-2-phenyl-2H-pyrazolo[3,4-b]pyridin-3-ol |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
4-Methoxy-2-[(4-piperidylpiperidyl)methyl]phenol |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
N-(5-Isopropyl-1,3,4-thiadiazol-2-yl)-3-nitrobenzamide |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
2-Amino-6-ethyl-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxamide |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
(NE)-N-[[3-[[3-[(E)-hydroxyiminomethyl]-2,4,6-trimethylphenyl]methyl]-2,4,6-trimethylphenyl]methylidene]hydroxylamine |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
N-(3-Fluorophenyl)-2,4,6-tri(propan-2-yl)benzenesulfonamide |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
2-(4-Hydroxy-3-methoxybenzylidene)-1H-indene-1,3(2H)-dione |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
2-[2-(5-Hydroxy-1H-indol-3-yl)ethyl]-1H-isoindole-1,3(2H)-dione |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
2-Furancarboxamide, N-[[(4-methoxyphenyl)amino]thioxomethyl]- |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
2-Amino-N-quinolin-8-yl-benzenesulfonamide |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
(5Z)-5-[(4-Fluorophenyl)methylidene]-1-methyl-3-phenyl-1,3-diazinane-2,4,6-trione |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
2-[4-(1-Adamantyl)phenoxy]-N,N-diethylethanamine;hydrochloride |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
(2Z)-2-(Acetylamino)-N-(4-hydroxyphenyl)-3-phenylprop-2-enamide |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
(5E)-5-[(3-Bromo-4-methoxyphenyl)methylidene]-1-phenyl-2-sulfanylidene-1,3-diazinane-4,6-dione |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
[(3-{[(4-Bromophenyl)amino]carbonyl}phenyl)thio]acetic acid |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
2-[(4-Chlorobenzyl)thio]-6,7-dihydro-5H-pyrrolo[1,2-a]imidazole |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
1-(5-Hydroxy-2-methyl-1-phenyl-1H-indol-3-yl)ethanone |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
2-[(4-Ethylpiperazin-1-yl)methyl]-4-methoxyphenol |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
4-(4-Fluorophenyl)-1,3,5-trimethyl-2,6-diphenylpiperidin-4-ol |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
N-[(E)-1-[5-(4-Bromophenyl)furan-2-yl]-3-[3-(dimethylamino)propylamino]-3-oxoprop-1-en-2-yl]-4-methylbenzamide |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
(2Z)-3-{N-[4-(4-Chlorophenyl)phenyl]carbamoyl}prop-2-enoic acid |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
4-[(E)-3-(4-Ethylpiperazin-1-yl)prop-1-enyl]-N,N-dimethylaniline |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
1,5-Dihydro-4,5-diphenyl-2H-imidazol-2-one |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
2-[(E)-2-(4-Chlorophenyl)ethenyl]-1-methyl-1H-benzimidazole |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
4-[1-Azabicyclo[2.2.2]octan-3-ylidene-[4-(dimethylamino)phenyl]methyl]-N,N-dimethylaniline;hydrochloride |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
4-Oxo-4-((4-(styryl)phenyl)amino)but-2-enoic acid |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
2,5-Dianilinoterephthalic acid |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
4-Methoxy-N-[4-(thiazol-2-ylsulfinamoyl)-phenyl]-benzamide |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
3-[(3,4-Dimethylphenyl)sulfonyl]propanenitrile |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
4-[4-(1,3-Benzoxazol-2-yl)anilino]-4-oxobutanoic acid |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
1-(3-Chlorophenyl)-2,3,4,5,6,7,8,8a-octahydro-1H-isoquinolin-4a-ol;hydrochloride |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
6-Methyl-2-(1,2,2,2-tetrafluoroethyl)-1H-benzimidazole |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
Ethyl 6-amino-5-cyano-2-methyl-4-(2-nitrophenyl)-4H-pyran-3-carboxylate |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
N-(2,1,3-Benzoxadiazol-4-yl)-2,2,2-trifluoroacetamide |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
4-Tert-butyl-N-(4-methylphenyl)benzamide |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
2-Methoxy-4-(morpholin-4-ylmethyl)phenol |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
Bis((1E)-2-phenylvinyl)phosphinic acid |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
1-[2-(Allyloxy)benzyl]-4-benzylpiperidine |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
2,5-Diaminoterephthalic acid |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
N-(1-Adamantylcarbonyl)-N'-(3-cyano-4,5,6,7-tetrahydro-1-benzothien-2-yl)thiourea |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
2-(Isobutylthio)succinic acid |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
N-{4-[Acetyl(methyl)amino]phenyl}-4-biphenylcarboxamide |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
4-[(E)-3-(2-Ethylpiperidin-1-yl)prop-1-enyl]-N,N-dimethylaniline |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
3-(2-Chloro-phenyl)-2-(4-(2-oxo-2H-chromen-3-YL)-thiazol-2-YL)-acrylonitrile |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
Ethyl (7Z)-2-amino-7-(hydroxyimino)-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxylate |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
2-Amino-4-(3,4-dichlorophenyl)thiazole |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
5-(2-Nitrobenzylidene)-2-thioxodihydropyrimidine-4,6(1H,5H)-dione |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
3-(4-Bromo-2-thienyl)-2-cyano-2-propenethioamide |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
Benzyl [(6-amino-3,5-dicyano-4-ethylpyridin-2-yl)sulfanyl]acetate |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
N-{2-[(1,3-Diphenyl-1H-pyrazol-5-yl)amino]phenyl}benzamide |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
2-Butyl-5-methylisophthalic acid |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
2-Butylsulfanyl-6-methyl-9H-1,3,4,9-tetraaza-fluorene |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
2-Phenyldipyrrolo[1,2-a:2',1'-c]pyrazine |
∼2.5 µM |
|
rat |
skeletal muscle mitochondria |
measurement of superoxide/H2O2 production |
affect |
Positive |
|
162 |
Fluoroacetate |
|
|
|
|
|
affect |
Positive |
|
173 |
Rosiglitazone |
1uM |
24 and 48 hours |
Murine |
3T3-L1 adipocytes differentiated |
96-well BD Oxygen Biosensor System plates |
increase |
Positive |
|
179 |
Rosiglitazone |
1uM |
24 and 48 hours |
Murine |
adipocytes |
Citrate Synthase Activity |
affect |
Positive |
|
179 |
atorvastatin |
|
|
|
C2C12 myoblasts |
|
affect |
Positive |
|
180 |
lovastatin |
|
|
|
C2C12 myoblasts |
|
affect |
Positive |
|
180 |
Simvastatin |
|
|
|
C2C12 myoblasts |
|
affect |
Positive |
|
180 |
Cerivastatin |
100uM |
|
|
C2C12 myoblasts |
measured ubiquinol:cytochrome c oxidoreductase activity in broken C2C12 mitochondria after acute statin exposure at a fixed concentration for all compounds |
decrease |
Positive |
|
180 |
pitavastatin |
100uM |
|
|
C2C12 myoblasts |
measured ubiquinol:cytochrome c oxidoreductase activity in broken C2C12 mitochondria after acute statin exposure at a fixed concentration for all compounds |
decrease |
Positive |
|
180 |
lovastatin |
100uM |
|
|
C2C12 myoblasts |
measured ubiquinol:cytochrome c oxidoreductase activity in broken C2C12 mitochondria after acute statin exposure at a fixed concentration for all compounds |
decrease |
Positive |
|
180 |
Simvastatin |
100uM |
|
|
C2C12 myoblasts |
Measured ubiquinol:cytochrome c oxidoreductase activity in broken C2C12 mitochondria after acute statin exposure at a fixed concentration for all compounds. The lactone forms of the indicated statins were included in the assay medium at their cytotoxic EC50 concentration for measurement of their effect on the catalytic capacity. |
decrease |
Positive |
|
180 |
Simvastatin |
200uM |
|
bovine |
heart mitochondria |
Reduction of the CIII cytochromes c1 and b was determined spectrophotometrically in bovine heart mitochondria. |
affect |
Positive |
p < 0.01 |
180 |
Diazoxide |
EC50= 40mmol/L, saturation by 100mmol/L |
|
|
Primary Culture of Neonatal Rat Cardiac Ventricular Myocytes |
flow cytometry and quantitative image analysis of cells stained with fluorescent DC indicators. |
affect |
Positive |
|
188 |
Pinacidil |
|
|
|
|
|
affect |
Positive |
|
188 |
5-Hydroxydecanoate |
500mmol/L |
|
|
Primary Culture of Neonatal Rat Cardiac Ventricular Myocytes |
flow cytometry and quantitative image analysis of cells stained with fluorescent DC indicators. |
affect |
Positive |
|
188 |
Glibenclamide |
|
|
|
|
|
affect |
Positive |
|
188 |
5-Hydroxydecanoate |
100 μm |
|
|
|
|
decrease |
Positive |
|
189 |
Glibenclamide |
K1/2 values 1-6 microM |
|
|
heart and liver mitochondria from rat |
|
affect |
Positive |
|
190 |
5-Hydroxydecanoate |
K1/2 values 45-75 microM |
|
|
heart and liver mitochondria from rat |
|
decrease |
Positive |
|
190 |
ionomycin |
|
|
rat |
liver mitochondria |
Oxygen consumption and medium pH were monitored simultaneously with a dual channel Gilson oxygraph equipped with a Clark electrode (Yellow Springs Instruments) and a combination pH electrode (Beckman No. 39030). |
increase |
Positive |
|
202 |
Troglitazone |
|
|
human |
hepatocytes |
ATP bioluminescence assay |
decrease |
Positive |
|
226 |
Troglitazone |
|
|
|
|
|
affect |
Positive |
|
227 |
Valproic Acid |
|
|
|
|
|
affect |
Positive |
|
227 |
Amiodarone |
|
|
|
|
|
affect |
Positive |
|
227 |
Tamoxifen |
|
|
|
|
|
affect |
Positive |
|
227 |
Tamoxifen |
|
|
|
|
|
affect |
Positive |
|
227 |
Perhexiline |
|
|
|
|
|
affect |
Positive |
|
227 |
Perhexiline |
|
|
rat |
hepatocytes |
|
affect |
Positive |
|
238 |
Acetaminophen |
|
|
|
|
|
affect |
Positive |
|
227 |
Salicylic acid |
|
|
|
|
|
affect |
Positive |
|
227 |
Ibuprofen |
|
|
|
|
|
affect |
Positive |
|
227 |
buprenorphine |
100 μM |
|
rat |
liver mitochondria |
the mitochondrial membrane potential assessed by the fluorescence of safranine. |
affect |
Positive |
|
235 |
Tianeptine |
0.0625 mmol/kg i.p. |
|
mouse |
|
in vivo |
affect |
Positive |
|
237 |
Tianeptine |
0.5 mM |
|
mouse |
|
The activity of the tricarboxylic acid cycle, assessed as the in vitro formation of [14C]CO2 from [1-14C]acetylcoenzyme A in vitro. |
affect |
Positive |
|
237 |
tetracyclines |
|
|
mouse |
liver mitochondria |
|
affect |
Positive |
|
236 |
tetracyclines |
|
|
mouse |
liver mitochondria |
Tricarboxylic acid cycle activity was assessed by the in vitro formation of [14C]CO2 from [1-14C]acetylcoenzyme A by mouse liver mitochondria. |
affect |
Positive |
|
236 |
Ibuprofen |
|
|
|
|
|
affect |
Positive |
|
239 |
Perhexiline |
77 μmol/L |
|
rat |
cardiac mitochondria |
CPT-1 activity was measured by the formation of palmitoyl-[3H]-carnitine from palmitoyl-CoA and [3H]-I- carnitine, |
affect |
Positive |
IC50 |
240 |
Perhexiline |
148 μmol/L |
|
rat |
hepatic mitochondria |
CPT-1 activity was measured by the formation of palmitoyl-[3H]-carnitine from palmitoyl-CoA and [3H]-I- carnitine, |
affect |
Positive |
IC50 |
240 |
Amiodarone |
228 μmol/L |
|
rat |
cardiac and hepatic mitochondria |
CPT-1 activity was measured by the formation of palmitoyl-[3H]-carnitine from palmitoyl-CoA and [3H]-I- carnitine, |
affect |
Positive |
IC50 |
240 |
Acetaminophen |
>400μM |
>400 |
mice |
Lean mice vs Ob/ob mice |
Measurement of oxygen consumption in the presence of ADP (state 3) and the different substrates was carried out on the Mitologics screening platform |
|
Positive |
EC20 |
227 |
Carbamazepine |
>400μM |
341 |
mice |
Lean mice vs Ob/ob mice |
Measurement of oxygen consumption in the presence of ADP (state 3) and the different substrates was carried out on the Mitologics screening platform |
|
Positive |
EC20 |
227 |
Diclofenac |
47μM |
11* |
mice |
Lean mice vs Ob/ob mice |
Measurement of oxygen consumption in the presence of ADP (state 3) and the different substrates was carried out on the Mitologics screening platform |
|
Positive |
EC20 |
227 |
Ibuprofen |
287μM |
80* |
mice |
Lean mice vs Ob/ob mice |
Measurement of oxygen consumption in the presence of ADP (state 3) and the different substrates was carried out on the Mitologics screening platform |
|
Positive |
EC20 |
227 |
Irinotecan |
6μM |
10 |
mice |
Lean mice vs Ob/ob mice |
Measurement of oxygen consumption in the presence of ADP (state 3) and the different substrates was carried out on the Mitologics screening platform |
|
Positive |
EC20 |
227 |
Methotrexate |
44μM |
42 |
mice |
Lean mice vs Ob/ob mice |
Measurement of oxygen consumption in the presence of ADP (state 3) and the different substrates was carried out on the Mitologics screening platform |
|
Positive |
EC20 |
227 |
Salicylic acid |
>400μM |
>400 |
mice |
Lean mice vs Ob/ob mice |
Measurement of oxygen consumption in the presence of ADP (state 3) and the different substrates was carried out on the Mitologics screening platform |
|
Positive |
EC20 |
227 |
Tamoxifen |
4μM |
11 |
mice |
Lean mice vs Ob/ob mice |
Measurement of oxygen consumption in the presence of ADP (state 3) and the different substrates was carried out on the Mitologics screening platform |
|
Positive |
EC20 |
227 |
Zidovudine |
79μM |
83 |
mice |
Lean mice vs Ob/ob mice |
Measurement of oxygen consumption in the presence of ADP (state 3) and the different substrates was carried out on the Mitologics screening platform |
|
Positive |
EC20 |
227 |
SB202190 |
10 μM |
|
|
intact and in permeabilized HeLa cells (MM5 cells expressing mitmutAEQ ) |
mitochondrial Ca2+ uptake |
increase |
Positive |
|
233 |
kaempferol |
1μM |
|
|
|
The HeLa cell clone MM5 expressing mitochondrially targeted mutated aequorin was used for [Ca2+]M measurements. [Ca2+]c measurements were carried out using HeLa cells transiently transfected with the plasmid for cytosolic aequorin. |
increase |
Positive |
|
234 |
kaempferol |
7μM |
|
|
|
The HeLa cell clone MM5 expressing mitochondrially targeted mutated aequorin was used for [Ca2+]M measurements. [Ca2+]c measurements were carried out using HeLa cells transiently transfected with the plasmid for cytosolic aequorin. |
increase |
Positive |
EC50 |
234 |
quercetin |
21 μM |
|
|
|
mitochondrial Ca2+ uptake |
increase |
Positive |
EC50 |
234 |
genistein |
37μM |
|
|
|
mitochondrial Ca2+ uptake |
increase |
Positive |
EC50 |
234 |
CGP37157 |
1 μmol/L |
|
|
periodically paced rat ventricular myocytes (VMs) under β-adrenergic stimulation |
mitochondrial Ca2+ monitored by mitochondrial-targeted Ca2+ biosensor mtRCamp1h. |
|
Positive |
|
241 |
kaempferol |
10 μmol/L |
|
|
periodically paced rat ventricular myocytes (VMs) under β-adrenergic stimulation |
mitochondrial Ca2+ monitored by mitochondrial-targeted Ca2+ biosensor mtRCamp1h. |
|
Positive |
|
241 |
CGP37157 |
1 μmol/L |
|
|
|
|
|
Positive |
|
241 |
Ru360 |
2 μmol/L |
|
|
|
|
|
Positive |
|
241 |
atpenin a5 |
|
|
bovine |
heart mitochondria |
|
affect |
Positive |
|
192 |
Carboxin |
|
|
bovine |
heart mitochondria |
|
affect |
Positive |
|
192 |
Thenoyltrifluoroacetone |
|
|
bovine |
heart mitochondria |
|
affect |
Positive |
|
192 |
HQNO |
|
|
bovine |
heart mitochondria |
|
affect |
Positive |
|
192 |
Nimesulide |
|
|
|
|
|
|
Positive |
|
197 |
lumiracoxib |
|
|
|
|
|
|
Positive |
|
197 |
Chloramphenicol |
|
|
|
|
|
|
Positive |
|
197 |
Cephaloglycin |
|
|
|
|
|
inhibit |
Positive |
|
197 |
Imipenem |
|
|
|
|
|
inhibit |
Positive |
|
197 |
Chlorpromazine |
|
|
|
|
|
inhibit |
Positive |
|
197 |
Haloperidol |
|
|
|
|
|
inhibit |
Positive |
|
197 |
Clozapine |
|
|
|
|
|
inhibit |
Positive |
|
197 |
Amitriptyline |
|
|
|
|
|
|
Positive |
|
197 |
Desipramine |
|
|
|
|
|
|
Positive |
|
197 |
Nefazodone |
|
|
|
|
|
inhibit |
Positive |
|
197 |
Metformin |
|
|
|
|
|
inhibit |
Positive |
|
197 |
Phenformin |
|
|
|
|
|
inhibit |
Positive |
|
197 |
Troglitazone |
|
|
|
|
|
inhibit |
Positive |
|
197 |
Rosiglitazone |
|
|
|
|
|
inhibit |
Positive |
|
197 |
Pioglitazone |
|
|
|
|
|
inhibit |
Positive |
|
197 |
Doxorubicin |
|
|
|
|
|
|
Positive |
|
197 |
Efavirenz |
|
|
|
|
|
|
Positive |
|
197 |
Propofol |
|
|
|
|
|
|
Positive |
|
197 |
Barbiturate |
|
|
|
|
|
decrease |
Positive |
|
197 |
Chlorpyrifos |
30–50 μM |
|
|
PC12 cell line |
we measured the concentration malondialdehyde (MDA) to indicate formation of lipid peroxides |
|
Positive |
|
242 |
Paraquat |
10 mg/kg/week intraperitoneal (i.p.) |
3weeks |
C57BL/6 mice |
|
|
|
Positive |
|
242 |
Rotenone |
10–100 nmol |
|
|
SK-N-MC Neuroblastoma cells |
|
decrease |
Positive |
|
242 |
Lead |
1%,2%,4% in oral chow |
|
Wistar rats |
|
|
|
Positive |
|
242 |
Aluminium |
100 mg/kg in drinking water daily for six weeks |
|
Wistar rats |
|
|
|
Positive |
|
242 |
Fluoroacetate |
|
|
|
|
|
|
Positive |
|
251 |
2-Deoxy-D-glucose |
|
|
|
|
|
|
Positive |
|
249 |
Lonidamine |
|
|
|
|
|
|
Positive |
|
249 |
Lonidamine |
|
|
|
|
|
|
Positive |
|
249 |
3-Bromopyruvate |
|
|
|
|
|
|
Positive |
|
249 |
Imatinib |
|
|
|
|
|
|
Positive |
|
249 |
Oxythiamine |
|
|
|
|
|
|
Positive |
|
249 |
Yohimbine |
|
|
mouse |
neuron |
Oxygen consumption rate (OCR) or extracellular acidification rate (ECAR) measurements from permeabilized neurons and isolated brain mitochondria were performed using the XF96 Extracellular Flux analyzer (Seahorse Bioscience). |
increase |
Positive |
|
269 |
Dyclonine |
|
|
mouse |
neuron |
Oxygen consumption rate (OCR) or extracellular acidification rate (ECAR) measurements from permeabilized neurons and isolated brain mitochondria were performed using the XF96 Extracellular Flux analyzer (Seahorse Bioscience). |
increase |
Positive |
|
269 |
Dronedarone |
10µM |
24hr |
|
isolated rat liver mitochondria, and the human hepatoma cell line HepG2 |
|
inhibit |
Positive |
|
271 |
Amiodarone |
20µM |
24hr |
|
isolated rat liver mitochondria, and the human hepatoma cell line HepG2 |
|
inhibit |
Positive |
|
271 |
Trimetazidine |
10-100µM |
|
rat |
isolated cardiac mitochondria |
|
increase |
Positive |
|
274 |
Valproic Acid |
0.5–2 mM |
3min |
rat |
inverted submitochondrial vesicles (ISMV) from rat liver isolated mitochondria |
The rate of the radiolabeled substrate [1-14C]-pyruvate uptake by ISMV was measured in the presence or absence of an inwardly directed proton gradient. |
inhibitor |
Positive |
|
279 |
alpha-Cyano-4-hydroxycinnamate |
1mM |
3min |
rat |
inverted submitochondrial vesicles (ISMV) from rat liver isolated mitochondria |
The rate of the radiolabeled substrate [1-14C]-pyruvate uptake by ISMV was measured in the presence or absence of an inwardly directed proton gradient. |
inhibitor |
Positive |
|
279 |
alpha-Cyano-4-hydroxycinnamate |
0.05mM |
|
|
|
|
inhibitor |
Positive |
>90% inhibition |
280 |
Alpha-Cyanocinnamate |
0.05mM |
|
|
|
|
inhibitor |
Positive |
>90% inhibition |
280 |
ranolazine |
25μM |
24hr |
|
T47D cells |
quantifies the conversion of [9,10-3H(N)]-palmitic acid to 3H2O with diffusion |
stimulate |
Positive |
Student’s two-tail t-test, where p < 0.05 |
273 |
Trimetazidine |
100 μM |
24hr |
|
T47D cells |
quantifies the conversion of [9,10-3H(N)]-palmitic acid to 3H2O with diffusion |
stimulate |
Positive |
Student’s two-tail t-test, where p < 0.05 |
273 |
Etomoxir |
0.1 to 50 μM |
24hr |
|
MCF-7 and T47D cells |
quantifies the conversion of [9,10-3H(N)]-palmitic acid to 3H2O with diffusion |
inhibition |
Positive |
Student’s two-tail t-test, where p < 0.05 |
273 |
Oxfenicine |
1.5 to 4.5mM |
24hr |
|
T47D cells |
quantifies the conversion of [9,10-3H(N)]-palmitic acid to 3H2O with diffusion |
inhibition |
Positive |
Student’s two-tail t-test, where p < 0.05 |
273 |
Carnitine |
0.5mM |
24hr |
|
U-937, MCF-7, and T47D |
quantifies the conversion of [9,10-3H(N)]-palmitic acid to 3H2O with diffusion |
stimulate |
Positive |
|
273 |
AICAR |
1mM |
24hr |
|
U-937, MCF-7, and T47D |
quantifies the conversion of [9,10-3H(N)]-palmitic acid to 3H2O with diffusion |
stimulate |
Positive |
|
273 |
AICAR |
|
|
|
|
|
stimulate |
Positive |
|
273 |
iodoacetate |
|
|
|
|
|
inhibition |
Positive |
|
278 |
Dichloroacetate |
|
|
|
|
|
inhibition |
Positive |
|
278 |
tacrolimus |
50 µg/ml |
12hr |
|
INS-1 cells |
XF24 Extracellular Flux Analyzer |
decrease |
Positive |
|
322 |
tacrolimus |
50 µg/ml |
12hr |
|
INS-1 cells |
XF24 Extracellular Flux Analyzer |
decrease |
Positive |
|
322 |
tacrolimus |
50 µg/ml |
12hr |
|
INS-1 cells |
XF24 Extracellular Flux Analyzer |
decrease |
Positive |
|
322 |
tacrolimus |
50 µg/ml |
12hr |
|
INS-1 cells |
XF24 Extracellular Flux Analyzer |
decrease |
Positive |
|
322 |
tacrolimus |
1 μM |
|
rat |
isolated kidney mitochondria |
Oxygen consumption was measured with a Clark‐type electrode |
decrease |
Positive |
10% |
323 |
rapamycin |
1 μM |
|
rat |
isolated kidney mitochondria |
Oxygen consumption was measured with a Clark‐type electrode |
decrease |
Positive |
11% |
323 |
tacrolimus |
3.4E−11 M and 2.3E−8 M |
|
rat |
isolated kidney mitochondria |
Oxygen consumption was measured with a Clark‐type electrode |
decrease |
Positive |
EC50 ; maximal inhibitory effect was about 20% |
323 |
rapamycin |
4.4×10−10 M |
|
rat |
isolated kidney mitochondria |
Oxygen consumption was measured with a Clark‐type electrode |
decrease |
Positive |
EC50 ; maximal inhibitory effect was about14% |
323 |
tacrolimus |
1 μM |
|
rat |
isolated kidney mitochondria |
Oxygen consumption was measured with a Clark‐type electrode |
decrease |
Positive |
|
323 |
rapamycin |
1 μM |
|
rat |
isolated kidney mitochondria |
Oxygen consumption was measured with a Clark‐type electrode |
decrease |
Positive |
|
323 |
MG-132 |
20 μM |
24 hr |
rat |
PC12 cells |
The total glutathione (reduced form GSH + oxidized form GSSG) was determined using glutathione reductase |
deplete GSH |
Positive |
|
289 |
3-morpholinosydnonimine |
150 μM |
24 hr |
rat |
PC12 cells |
The total glutathione (reduced form GSH + oxidized form GSSG) was determined using glutathione reductase |
restore GSH |
Positive |
|
289 |
MG-132 |
20 μM |
6 hr |
|
HeLa cells |
Total ubiquitin, Lysine 48-linked polyubiquitin and Lysine 63-linked polyubiquitin levels were assessed in whole cell extracts by western blotting. |
increase |
Positive |
|
291 |
MG-132 |
20 μM |
6 hr |
|
HeLa cells |
Mitochondrial respiration was calculated by measuring oxygen consumption rate (OCR) and proton flux under a series of conditions using a Seahorse Flux analyzer. |
inhibit |
Positive |
|
291 |
Diazepam |
70 μg/ml |
|
|
pig kidney embryo cells |
polarographic cell (1.2 ml) |
inhibit |
Positive |
|
293 |
Diazepam |
150μg/ml |
2hr |
|
PE cells |
luciferin-luciferase method |
decrease |
Positive |
|
293 |
Cadmium |
50-500 μM |
3hr |
rat |
PC12 cells |
Cell respiration was determined polarographically with the help of Clark oxygen electrode |
decrease |
Positive |
|
300 |
Mercury |
10-50 μM |
3hr |
rat |
PC12 cells |
Cell respiration was determined polarographically with the help of Clark oxygen electrode |
decrease |
Positive |
|
300 |
Copper |
50 μM |
|
rat |
PC12 cells |
Cell respiration was determined polarographically with the help of Clark oxygen electrode |
decrease |
Positive |
|
300 |
MCU-i4 |
5 μM |
|
|
HeLa cells transfected with mitochondria-targeted aequorin (mtAeq) after cellular stimulation with histamine |
Highigh-throughput screening assay based on aequorin. |
decrease |
Positive |
|
301 |
MCU-i11 |
5 μM |
|
|
HeLa cells transfected with mitochondria-targeted aequorin (mtAeq) after cellular stimulation with histamine |
Highigh-throughput screening assay based on aequorin. |
decrease |
Positive |
|
301 |
MCU-i4 |
10 μM |
|
|
mouse embryonic fibroblasts (MEFs), MDA-MB-231, and HEK293T cell lines |
Small-Scale Validation Assay (cytoplasmic- or mitochondria-targeted aequorin (cytAeq and mtAeq, respectively) |
decrease |
Positive |
|
301 |
MCU-i11 |
10 μM |
|
|
mouse embryonic fibroblasts (MEFs), MDA-MB-231, and HEK293T cell lines |
Small-Scale Validation Assay (cytoplasmic- or mitochondria-targeted aequorin (cytAeq and mtAeq, respectively) |
decrease |
Positive |
|
301 |
MCU-i4 |
8.4 μM(Micu1), 18 μM (Micu1-Micu2) |
|
|
Purified recombinant Micu1, Micu2 |
Purified recombinant Micu1, Micu2, and the dimeric Micu1-Micu2 proteins were immobilized on different channels of a SPR sensor chip surface. |
decrease |
Positive |
IC50 |
301 |
MCU-i11 |
2.9 μM(Micu1), 2.7 μM (Micu1-Micu2) |
|
|
Purified recombinant Micu1, Micu2 |
Purified recombinant Micu1, Micu2, and the dimeric Micu1-Micu2 proteins were immobilized on different channels of a SPR sensor chip surface. |
decrease |
Positive |
IC50 |
301 |
MCU-i4 |
10 μM |
|
|
Skeletal Muscle Fibers |
measured mitochondrial Ca2+ uptake in flexor digitorum brevis (FDB) myofibers freshly isolated from adult mice and previously transfected in vivo with the mitochondria-targeted Ca2+ probe 4mt-GCaMP6f |
decrease |
Positive |
|
301 |
MCU-i11 |
10 μM |
|
|
Skeletal Muscle Fibers |
measured mitochondrial Ca2+ uptake in flexor digitorum brevis (FDB) myofibers freshly isolated from adult mice and previously transfected in vivo with the mitochondria-targeted Ca2+ probe 4mt-GCaMP6f |
decrease |
Positive |
|
301 |
DS16570511 |
7 μM |
|
|
HEK293A cells |
HEK293A cell lines expressing the mitochondria-targeted Ca2+ indicator protein aequorin |
decrease |
Positive |
IC50 |
302 |
Ketoconazole |
I50=32, 74, 65, 75, 500μM for substrates Glutamate/Malate, Pyruvate/Malate, Ornithine/Malate, Arginine/Malate and Succinate repectively |
|
rat |
liver mitochondria |
Clark electrode |
inhibit |
Positive |
|
303 |
Miconazole |
I50=100, 160, 160, 170, 150 μM for substrates Glutamate/Malate, Pyruvate/Malate, Ornithine/Malate, Arginine/Malate and Succinate repectively |
|
rat |
liver mitochondria |
Clark electrode |
inhibit |
Positive |
|
303 |
amphotericin B |
2.5mg/ml |
|
Aspergillus fumigatus |
|
the formation of MDAs by antifungal drug-derived ROS in A. fumigatus was determined using the thiobarbituric acid (TBA) assay. |
induce |
Positive |
|
304 |
Terbinafine |
4mg/ml |
|
Aspergillus fumigatus |
|
lipid peroxidation using the thiobarbituric acid assay |
induce |
Positive |
|
304 |
itraconazole |
4mg/ml |
|
Aspergillus fumigatus |
|
lipid peroxidation using the thiobarbituric acid assay |
induce |
Positive |
|
304 |
amphotericin B |
2.5mg/ml |
|
Aspergillus fumigatus |
|
mitochondrion-specific lipid peroxidation probe MitoPerOx |
induce |
Positive |
|
304 |
Terbinafine |
4mg/ml |
3min, 5min, 15min |
Aspergillus fumigatus |
|
mitochondrion-specific lipid peroxidation probe MitoPerOx |
induce |
Positive |
|
304 |
itraconazole |
4mg/ml |
|
Aspergillus fumigatus |
|
mitochondrion-specific lipid peroxidation probe MitoPerOx |
induce |
Positive |
|
304 |
neomycin |
400 μM |
|
zebrafish |
zebrafish lateral line hair |
measrueing cytoplasmic oxidation (HyPer) and mitochondrial Ca2+ uptake (mitoRGECO) |
increase |
Positive |
|
315 |
Gentamicin |
300 μg/ml |
1hr |
postnatal day 6 (P6±1d) FVB mice |
basal turn outer hair cells ( low-frequency processing OHCs) from intact cochlear (organ of Corti) explants |
scanning confocal microscope (NADH autofluorescence); T1 imaging buffer contained 5 mM glucose. T2 imaging buffer contained 10 mM glucose, 3 mM glutamate and 2 mM pyruvate. |
decrease |
Positive |
|
312 |
Gentamicin |
5mM |
10min |
rat |
isolated rat liver (and kidney) mitochondria |
Oroboros O2K Oxygraph, complex II-based state 4 respiration |
increase |
Positive |
|
316 |
Gentamicin |
5mM |
10min |
rat |
isolated rat liver (and kidney) mitochondria |
Oroboros O2K Oxygraph, complex II-based state 3u respiration |
decrease |
Positive |
|
316 |
Gentamicin |
5mM |
10min |
rat |
isolated rat liver mitochondria |
Oroboros O2K Oxygraph, complex I-based state 4 respiration |
increase |
Positive |
|
316 |
Gentamicin |
5mM |
10min |
rat |
isolated rat liver mitochondria |
Oroboros O2K Oxygraph, complex I-based state 3u respiration |
decrease |
Positive |
|
316 |
Gentamicin |
5mM |
10min |
rat |
isolated rat liver (and kidney) mitochondria |
Oroboros O2K Oxygraph |
reduce |
Positive |
|
316 |
Berberine |
1-10 µM |
|
|
isolated rat muscle mitochondria |
Clark type oxygen electrode (Strathkelvin Instruments) |
decrease |
Positive |
|
328 |
Berberine |
25 μM |
48, 72 hr |
|
K1735-M2 mouse melanoma cells |
An acid extraction procedure was used to evaluate the intracellular concentration of adenine nucleotides. Adenine nucleotides were separated by reverse-phase high-performance liquid chromatography. Quantification was achieved by employing ATP, ADP, and AMP standard curves. |
decrease |
Positive |
p< 0.05 vs. control for each time of incubation |
327 |
Berberine |
10 μM |
24 hr |
|
K1735-M2 mouse melanoma cells |
An acid extraction procedure was used to evaluate the intracellular concentration of adenine nucleotides. Adenine nucleotides were separated by reverse-phase high-performance liquid chromatography. Quantification was achieved by employing ATP, ADP, and AMP standard curves. |
decrease |
Positive |
p< 0.05 vs. control for each time of incubation |
327 |
Acetaminophen |
348.5 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
Acetylsalicylic acid |
> 800 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
alpidem |
25.6 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
Amantadine |
> 400 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
Ambroxol |
> 400 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
Amiodarone |
45.92 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
Amoxicillin |
90.8 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
increase |
Positive |
EC20 |
36 |
Ampicillin |
> 400 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
Antipyrine |
> 400 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
Arsenic trioxide |
< 50 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
Biotin |
44.5 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
lumiracoxib |
> 400 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
bisacodyl |
50.9 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
estradiol acetate |
> 200 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
Bupivacaine |
60.6 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
Busulfan |
169.8 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
Butein |
29.6 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
Caffeine |
> 400 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
Capsaicin |
15 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
Carbamazepine |
53.4 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
Cefixime |
41.8 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
Chlorambucil |
138.7 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
Ciprofloxacin |
195.0 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
increase |
Positive |
EC20 |
36 |
Clodronate |
> 400 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
Clotrimazole |
2.9 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
curcumin |
> 200 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
Daunorubicin |
12.8 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
dexamethasone valerate |
> 200 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
Diazoxide |
4.9 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
Diclofenac |
9.1 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
Diflunisal |
9.8 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
Doxorubicin |
15.9 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
erlotinib |
328.8 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
Fluconazole |
> 400 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
Flufenamic Acid |
1.7 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
gefitinib |
269.6 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
genistein |
81.3 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
Glimepiride |
16.6 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
Gossypol |
30.3 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
Ibuprofen |
170.1 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
imipramine |
75.5 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
increase |
Positive |
EC20 |
36 |
Indomethacin |
25.2 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
Isoniazid |
59.8 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
Ketoconazole |
> 400 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
Lamivudine |
160.7 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
Lidocaine |
> 400 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
Lonidamine |
18.9 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
lovastatin |
4.4 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
lumiracoxib |
26.3 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
Manganese |
> 400 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
Mefenamic acid |
10.1 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
Metformin |
> 400 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
Mitomycin |
4.9 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
Nicotine |
> 400 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
nifuroxazide |
61.5 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
Nimesulide |
< 25 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
Nitrofurantoin |
232.3 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
Perhexiline |
88.4 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
Piroxicam |
224.5 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
pravastatin |
5 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
propylparaben |
63 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
Pyrazinamide |
107.5 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
resveratrol |
7.7 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
riboflavin |
264.6 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
rifampicin |
124.1 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
ritonavir |
35.5 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
Salicylic acid |
354.4 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
Simvastatin |
1.6 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
sorafenib |
283.4 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
Sulindac |
> 400 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
Tolfenamic Acid |
> 400 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
Troglitazone |
3.9 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
Valproic Acid |
> 400 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
Zidovudine |
> 800 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Rotenone (2µM) was used as 100% baseline for complex I inhibition. |
decrease |
Positive |
EC20 |
36 |
Acetaminophen |
> 400 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Oligomycin A (1µM) was used as 100% baseline for complex II inhibition. |
decrease |
Positive |
EC20 |
36 |
Acetylsalicylic acid |
149.8 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Oligomycin A (1µM) was used as 100% baseline for complex II inhibition. |
decrease |
Positive |
EC20 |
36 |
alpidem |
29.6 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Oligomycin A (1µM) was used as 100% baseline for complex II inhibition. |
decrease |
Positive |
EC20 |
36 |
Amantadine |
> 400 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Oligomycin A (1µM) was used as 100% baseline for complex II inhibition. |
decrease |
Positive |
EC20 |
36 |
Ambroxol |
> 200 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Oligomycin A (1µM) was used as 100% baseline for complex II inhibition. |
decrease |
Positive |
EC20 |
36 |
Amoxicillin |
188.8 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Oligomycin A (1µM) was used as 100% baseline for complex II inhibition. |
increase |
Positive |
EC20 |
36 |
Ampicillin |
161.2 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Oligomycin A (1µM) was used as 100% baseline for complex II inhibition. |
increase |
Positive |
EC20 |
36 |
Antipyrine |
> 400 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Oligomycin A (1µM) was used as 100% baseline for complex II inhibition. |
decrease |
Positive |
EC20 |
36 |
Arsenic trioxide |
0.9 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Oligomycin A (1µM) was used as 100% baseline for complex II inhibition. |
decrease |
Positive |
EC20 |
36 |
lumiracoxib |
> 400 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Oligomycin A (1µM) was used as 100% baseline for complex II inhibition. |
decrease |
Positive |
EC20 |
36 |
bisacodyl |
52.5 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Oligomycin A (1µM) was used as 100% baseline for complex II inhibition. |
decrease |
Positive |
EC20 |
36 |
estradiol acetate |
> 200 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Oligomycin A (1µM) was used as 100% baseline for complex II inhibition. |
decrease |
Positive |
EC20 |
36 |
Bupivacaine |
> 800 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Oligomycin A (1µM) was used as 100% baseline for complex II inhibition. |
decrease |
Positive |
EC20 |
36 |
Caffeine |
> 400 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Oligomycin A (1µM) was used as 100% baseline for complex II inhibition. |
decrease |
Positive |
EC20 |
36 |
Capsaicin |
15.7 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Oligomycin A (1µM) was used as 100% baseline for complex II inhibition. |
decrease |
Positive |
EC20 |
36 |
Carbamazepine |
170.8 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Oligomycin A (1µM) was used as 100% baseline for complex II inhibition. |
increase |
Positive |
EC20 |
36 |
Cefixime |
216.8 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Oligomycin A (1µM) was used as 100% baseline for complex II inhibition. |
decrease |
Positive |
EC20 |
36 |
Chlorambucil |
140.9 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Oligomycin A (1µM) was used as 100% baseline for complex II inhibition. |
decrease |
Positive |
EC20 |
36 |
Clodronate |
227.2 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Oligomycin A (1µM) was used as 100% baseline for complex II inhibition. |
decrease |
Positive |
EC20 |
36 |
curcumin |
> 200 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Oligomycin A (1µM) was used as 100% baseline for complex II inhibition. |
decrease |
Positive |
EC20 |
36 |
Daunorubicin |
10.9 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Oligomycin A (1µM) was used as 100% baseline for complex II inhibition. |
decrease |
Positive |
EC20 |
36 |
dexamethasone valerate |
> 200 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Oligomycin A (1µM) was used as 100% baseline for complex II inhibition. |
decrease |
Positive |
EC20 |
36 |
Diclofenac |
29.8 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Oligomycin A (1µM) was used as 100% baseline for complex II inhibition. |
decrease |
Positive |
EC20 |
36 |
erlotinib |
17.4 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Oligomycin A (1µM) was used as 100% baseline for complex II inhibition. |
increase |
Positive |
EC20 |
36 |
Fluconazole |
186.6 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Oligomycin A (1µM) was used as 100% baseline for complex II inhibition. |
decrease |
Positive |
EC20 |
36 |
Ibuprofen |
132.1 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Oligomycin A (1µM) was used as 100% baseline for complex II inhibition. |
decrease |
Positive |
EC20 |
36 |
imipramine |
18.3 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Oligomycin A (1µM) was used as 100% baseline for complex II inhibition. |
increase |
Positive |
EC20 |
36 |
Ketoconazole |
2.9 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Oligomycin A (1µM) was used as 100% baseline for complex II inhibition. |
decrease |
Positive |
EC20 |
36 |
Lamivudine |
317.4 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Oligomycin A (1µM) was used as 100% baseline for complex II inhibition. |
decrease |
Positive |
EC20 |
36 |
Lidocaine |
188.2 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Oligomycin A (1µM) was used as 100% baseline for complex II inhibition. |
increase |
Positive |
EC20 |
36 |
lovastatin |
6.2 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Oligomycin A (1µM) was used as 100% baseline for complex II inhibition. |
decrease |
Positive |
EC20 |
36 |
lumiracoxib |
12 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Oligomycin A (1µM) was used as 100% baseline for complex II inhibition. |
decrease |
Positive |
EC20 |
36 |
Manganese |
> 400 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Oligomycin A (1µM) was used as 100% baseline for complex II inhibition. |
decrease |
Positive |
EC20 |
36 |
Metformin |
351.8 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Oligomycin A (1µM) was used as 100% baseline for complex II inhibition. |
decrease |
Positive |
EC20 |
36 |
Nicotine |
312 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Oligomycin A (1µM) was used as 100% baseline for complex II inhibition. |
decrease |
Positive |
EC20 |
36 |
nifuroxazide |
3.7 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Oligomycin A (1µM) was used as 100% baseline for complex II inhibition. |
decrease |
Positive |
EC20 |
36 |
Nitrofurantoin |
8.7 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Oligomycin A (1µM) was used as 100% baseline for complex II inhibition. |
decrease |
Positive |
EC20 |
36 |
Perhexiline |
87.7 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Oligomycin A (1µM) was used as 100% baseline for complex II inhibition. |
decrease |
Positive |
EC20 |
36 |
Piroxicam |
6.6 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Oligomycin A (1µM) was used as 100% baseline for complex II inhibition. |
decrease |
Positive |
EC20 |
36 |
propylparaben |
28.4 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Oligomycin A (1µM) was used as 100% baseline for complex II inhibition. |
decrease |
Positive |
EC20 |
36 |
Pyrazinamide |
190.9 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Oligomycin A (1µM) was used as 100% baseline for complex II inhibition. |
decrease |
Positive |
EC20 |
36 |
riboflavin |
182.8 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Oligomycin A (1µM) was used as 100% baseline for complex II inhibition. |
decrease |
Positive |
EC20 |
36 |
Salicylic acid |
120.9 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Oligomycin A (1µM) was used as 100% baseline for complex II inhibition. |
decrease |
Positive |
EC20 |
36 |
Sulindac |
35.6 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Oligomycin A (1µM) was used as 100% baseline for complex II inhibition. |
decrease |
Positive |
EC20 |
36 |
Tolfenamic Acid |
238.7 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Oligomycin A (1µM) was used as 100% baseline for complex II inhibition. |
increase |
Positive |
EC20 |
36 |
Troglitazone |
6 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Oligomycin A (1µM) was used as 100% baseline for complex II inhibition. |
decrease |
Positive |
EC20 |
36 |
Valproic Acid |
44.9 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Oligomycin A (1µM) was used as 100% baseline for complex II inhibition. |
decrease |
Positive |
EC20 |
36 |
Zidovudine |
242.0 µM |
60 mins |
mouse |
liver mitochondria |
Oxygen consumption was monitored with 50nM MitoXpress ( an oxygen-sensitive phosphorescent dye) using a spectrofluorimeter (Tecan Infinite 200; λExcitation 380nm; λEmission 650nm). Oligomycin A (1µM) was used as 100% baseline for complex II inhibition. |
increase |
Positive |
EC20 |
36 |
Zidovudine |
|
|
|
|
|
Interfere |
Positive |
|
307 |
Acyclovir |
|
|
|
|
|
Interfere |
Positive |
|
307 |
Ganciclovir |
|
|
|
|
|
Interfere |
Positive |
|
307 |
Zalcitabine |
|
|
|
|
|
Interfere |
Positive |
|
307 |
Saquinavir |
|
|
|
|
|
Interfere |
Positive |
|
307 |
tetracyclines |
|
|
|
|
|
decrease |
Positive |
|
307 |
Ciprofloxacin |
|
|
|
|
|
decrease |
Positive |
|
307 |
Ciprofloxacin |
|
|
|
|
|
decrease |
Positive |
|
307 |
Ciprofloxacin |
|
|
|
|
|
Increase |
Positive |
|
307 |
Cisplatin |
|
|
|
|
|
decrease |
Positive |
|
307 |
Cyclophosphamide |
|
|
|
|
|
decrease |
Positive |
|
307 |
Clozapine |
|
|
|
|
|
decrease |
Positive |
|
307 |
sertraline |
|
|
rat |
brain mitochondria |
|
decrease |
Positive |
|
307 |
Fluoxetine |
|
|
rat |
brain mitochondria |
|
decrease |
Positive |
|
307 |
sertraline |
|
|
rat |
liver mitochondria |
|
decrease |
Positive |
|
307 |
Fluoxetine |
|
|
rat |
liver mitochondria |
|
decrease |
Positive |
|
307 |
sertraline |
|
|
|
|
|
decrease |
Positive |
|
307 |
Fluoxetine |
|
|
|
|
|
decrease |
Positive |
|
307 |
Flufenamic Acid |
2.9 ± 0.3 |
|
rat |
isolated rat liver mitochondria |
State 2 respiration ( 96-well plate format using a phosphorescent oxygen-sensitive probe MitoXpress) |
inhibit |
Positive |
UC50 (nmol/mg mitochondrial protein) |
40 |
Tolfenamic Acid |
3.4 ± 0.6 |
|
rat |
isolated rat liver mitochondria |
State 2 respiration ( 96-well plate format using a phosphorescent oxygen-sensitive probe MitoXpress) |
inhibit |
Positive |
UC50 (nmol/mg mitochondrial protein) |
40 |
Mefenamic acid |
17.9 ± 2.2 |
|
rat |
isolated rat liver mitochondria |
State 2 respiration ( 96-well plate format using a phosphorescent oxygen-sensitive probe MitoXpress) |
inhibit |
Positive |
UC50 (nmol/mg mitochondrial protein) |
40 |
Meloxicam |
22.8 ± 2.8 |
|
rat |
isolated rat liver mitochondria |
State 2 respiration ( 96-well plate format using a phosphorescent oxygen-sensitive probe MitoXpress) |
inhibit |
Positive |
UC50 (nmol/mg mitochondrial protein) |
40 |
Sudoxicam |
37.4 ± 3.0 |
|
rat |
isolated rat liver mitochondria |
State 2 respiration ( 96-well plate format using a phosphorescent oxygen-sensitive probe MitoXpress) |
inhibit |
Positive |
UC50 (nmol/mg mitochondrial protein) |
40 |
Piroxicam |
69.0 ± 7.2 |
|
rat |
isolated rat liver mitochondria |
State 2 respiration ( 96-well plate format using a phosphorescent oxygen-sensitive probe MitoXpress) |
inhibit |
Positive |
UC50 (nmol/mg mitochondrial protein) |
40 |
Diflunisal |
6.7 ± 1.3 |
|
rat |
isolated rat liver mitochondria |
State 2 respiration ( 96-well plate format using a phosphorescent oxygen-sensitive probe MitoXpress) |
inhibit |
Positive |
UC50 (nmol/mg mitochondrial protein) |
40 |
Diclofenac |
56.3 ± 4.9 |
|
rat |
isolated rat liver mitochondria |
State 2 respiration ( 96-well plate format using a phosphorescent oxygen-sensitive probe MitoXpress) |
inhibit |
Positive |
UC50 (nmol/mg mitochondrial protein) |
40 |
Sulindac |
> 100 |
|
rat |
isolated rat liver mitochondria |
State 2 respiration ( 96-well plate format using a phosphorescent oxygen-sensitive probe MitoXpress) |
inhibit |
Positive |
UC50 (nmol/mg mitochondrial protein) |
40 |
Sulindac sulfide |
25.7 ± 4.5 |
|
rat |
isolated rat liver mitochondria |
State 2 respiration ( 96-well plate format using a phosphorescent oxygen-sensitive probe MitoXpress) |
inhibit |
Positive |
UC50 (nmol/mg mitochondrial protein) |
40 |
Nimesulide |
2.6 ± 0.2 |
|
rat |
isolated rat liver mitochondria |
State 2 respiration ( 96-well plate format using a phosphorescent oxygen-sensitive probe MitoXpress) |
inhibit |
Positive |
UC50 (nmol/mg mitochondrial protein) |
40 |
Sulindac sulfide |
39.8 ± 2.9 |
|
rat |
isolated rat liver mitochondria |
State 3 respiration ( 96-well plate format using a phosphorescent oxygen-sensitive probe MitoXpress) |
inhibit |
Positive |
IC50 (nmol/mg mitochondrial protein) |
40 |
Flufenamic Acid |
146 |
24hr |
rat |
hepatocytes |
LipidTox, for neutral lipid accumulation, to evaluate lipid content. |
accumulation |
Positive |
AC50 (μM) |
40 |
Tolfenamic Acid |
83.1 |
24hr |
rat |
hepatocytes |
LipidTox, for neutral lipid accumulation, to evaluate lipid content. |
accumulation |
Positive |
AC50 (μM) |
40 |
Mefenamic acid |
161 |
24hr |
rat |
hepatocytes |
LipidTox, for neutral lipid accumulation, to evaluate lipid content. |
accumulation |
Positive |
AC50 (μM) |
40 |
Meloxicam |
> 500 |
24hr |
rat |
hepatocytes |
LipidTox, for neutral lipid accumulation, to evaluate lipid content. |
accumulation |
Positive |
AC50 (μM) |
40 |
Sudoxicam |
> 500 |
24hr |
rat |
hepatocytes |
LipidTox, for neutral lipid accumulation, to evaluate lipid content. |
accumulation |
Positive |
AC50 (μM) |
40 |
Piroxicam |
728 |
24hr |
rat |
hepatocytes |
LipidTox, for neutral lipid accumulation, to evaluate lipid content. |
accumulation |
Positive |
AC50 (μM) |
40 |
Diflunisal |
68 |
24hr |
rat |
hepatocytes |
LipidTox, for neutral lipid accumulation, to evaluate lipid content. |
accumulation |
Positive |
AC50 (μM) |
40 |
Diclofenac |
122 |
24hr |
rat |
hepatocytes |
LipidTox, for neutral lipid accumulation, to evaluate lipid content. |
accumulation |
Positive |
AC50 (μM) |
40 |
Sulindac sulfide |
78 |
24hr |
rat |
hepatocytes |
LipidTox, for neutral lipid accumulation, to evaluate lipid content. |
accumulation |
Positive |
AC50 (μM) |
40 |
Nimesulide |
29 |
24hr |
rat |
hepatocytes |
LipidTox, for neutral lipid accumulation, to evaluate lipid content. |
accumulation |
Positive |
AC50 (μM) |
40 |
Flufenamic Acid |
79 |
24hr |
rat |
hepatocytes |
glutathion depletion: cells were incubated with 50 μM monochlorobimane with 6 μg/ml Hoechst 33342 |
|
Positive |
AC50 (μM) |
40 |
Tolfenamic Acid |
105 |
24hr |
rat |
hepatocytes |
glutathion depletion: cells were incubated with 50 μM monochlorobimane with 6 μg/ml Hoechst 33342 |
|
Positive |
AC50 (μM) |
40 |
Mefenamic acid |
148 |
24hr |
rat |
hepatocytes |
glutathion depletion: cells were incubated with 50 μM monochlorobimane with 6 μg/ml Hoechst 33342 |
|
Positive |
AC50 (μM) |
40 |
Meloxicam |
316 |
24hr |
rat |
hepatocytes |
glutathion depletion: cells were incubated with 50 μM monochlorobimane with 6 μg/ml Hoechst 33342 |
|
Positive |
AC50 (μM) |
40 |
Sudoxicam |
313 |
24hr |
rat |
hepatocytes |
glutathion depletion: cells were incubated with 50 μM monochlorobimane with 6 μg/ml Hoechst 33342 |
|
Positive |
AC50 (μM) |
40 |
Diflunisal |
29 |
24hr |
rat |
hepatocytes |
glutathion depletion: cells were incubated with 50 μM monochlorobimane with 6 μg/ml Hoechst 33342 |
|
Positive |
AC50 (μM) |
40 |
Diclofenac |
167 |
24hr |
rat |
hepatocytes |
glutathion depletion: cells were incubated with 50 μM monochlorobimane with 6 μg/ml Hoechst 33342 |
|
Positive |
AC50 (μM) |
40 |
Sulindac |
896 |
24hr |
rat |
hepatocytes |
glutathion depletion: cells were incubated with 50 μM monochlorobimane with 6 μg/ml Hoechst 33342 |
|
Positive |
AC50 (μM) |
40 |
Sulindac sulfide |
40 |
24hr |
rat |
hepatocytes |
glutathion depletion: cells were incubated with 50 μM monochlorobimane with 6 μg/ml Hoechst 33342 |
|
Positive |
AC50 (μM) |
40 |
Nimesulide |
1 |
24hr |
rat |
hepatocytes |
glutathion depletion: cells were incubated with 50 μM monochlorobimane with 6 μg/ml Hoechst 33342 |
|
Positive |
AC50 (μM) |
40 |
Amiodarone |
75.2 ± 12.9, 92.0 ± 5.5, 0.8, 95.1 ± 10.1 ,69.1 ± 24.1, 1.3 |
4hr |
|
H9c2 cells |
high-glucose–galactose cell viability assay with JC-1 mitochondrial membrane potential and ATP-depletion assays (CellTiter-Glo reagent ). |
|
Positive |
glucose/galactose IC50 ratio (JC-1 IC50 in glucose, JC-1 IC50 in galactose, JC-1 glu/gla, ATP IC50 in glucose, ATP IC50 in galactose, ATP glu/gla ) |
50 |
Amitriptyline |
70.9 ± 16.8, 72.0 ± 5.3, 1, 68.1 ± 9.1, 67.0 ± 11.6, 1 |
4hr |
|
H9c2 cells |
high-glucose–galactose cell viability assay with JC-1 mitochondrial membrane potential and ATP-depletion assays (CellTiter-Glo reagent ). |
|
Positive |
glucose/galactose IC50 ratio (JC-1 IC50 in glucose, JC-1 IC50 in galactose, JC-1 glu/gla, ATP IC50 in glucose, ATP IC50 in galactose, ATP glu/gla ) |
50 |
Chlorpromazine |
36.6 ± 19.4, 48.4 ± 11.9, 0.8, 17.3 ± 7.6, 25.3 ± 10.8, 0.7 |
4hr |
|
H9c2 cells |
high-glucose–galactose cell viability assay with JC-1 mitochondrial membrane potential and ATP-depletion assays (CellTiter-Glo reagent ). |
|
Positive |
glucose/galactose IC50 ratio (JC-1 IC50 in glucose, JC-1 IC50 in galactose, JC-1 glu/gla, ATP IC50 in glucose, ATP IC50 in galactose, ATP glu/gla ) |
50 |
Fluoxetine |
63.4 ± 8.1, 43.1 ± 9.6 ,1.5, 58.0 ± 15.1, 63.3 ± 26.2, 0.9 |
4hr |
|
H9c2 cells |
high-glucose–galactose cell viability assay with JC-1 mitochondrial membrane potential and ATP-depletion assays (CellTiter-Glo reagent ). |
|
Positive |
glucose/galactose IC50 ratio (JC-1 IC50 in glucose, JC-1 IC50 in galactose, JC-1 glu/gla, ATP IC50 in glucose, ATP IC50 in galactose, ATP glu/gla ) |
50 |
Idarubicin |
7.9 ± 3.3 , 4.2 ± 2.0, 1.9, 11.5 ± 5.7 ,6.2 ± 4.0, 1.9 |
4hr |
|
H9c2 cells |
high-glucose–galactose cell viability assay with JC-1 mitochondrial membrane potential and ATP-depletion assays (CellTiter-Glo reagent ). |
|
Positive |
glucose/galactose IC50 ratio (JC-1 IC50 in glucose, JC-1 IC50 in galactose, JC-1 glu/gla, ATP IC50 in glucose, ATP IC50 in galactose, ATP glu/gla ) |
50 |
imipramine |
91.6 ± 18.2, 84.1 ± 10.3, 1.1, 71.4 ± 22.4, 90.3 ± 11.7, 0.8 |
4hr |
|
H9c2 cells |
high-glucose–galactose cell viability assay with JC-1 mitochondrial membrane potential and ATP-depletion assays (CellTiter-Glo reagent ). |
|
Positive |
glucose/galactose IC50 ratio (JC-1 IC50 in glucose, JC-1 IC50 in galactose, JC-1 glu/gla, ATP IC50 in glucose, ATP IC50 in galactose, ATP glu/gla ) |
50 |
mefloquine |
2.9 ± 1.1, 2.3 ± 1.0, 1.4 ,3.4 ± 1.3, 3.6 ± 2.2, 1.2 |
4hr |
|
H9c2 cells |
high-glucose–galactose cell viability assay with JC-1 mitochondrial membrane potential and ATP-depletion assays (CellTiter-Glo reagent ). |
|
Positive |
glucose/galactose IC50 ratio (JC-1 IC50 in glucose, JC-1 IC50 in galactose, JC-1 glu/gla, ATP IC50 in glucose, ATP IC50 in galactose, ATP glu/gla ) |
50 |
Menadione |
18.0 ± 7.2, 14.7 ± 7.9 ,1.2, 19.5 ± 8.3, 14.0 ± 8.7, 1.4 |
4hr |
|
H9c2 cells |
high-glucose–galactose cell viability assay with JC-1 mitochondrial membrane potential and ATP-depletion assays (CellTiter-Glo reagent ). |
|
Positive |
glucose/galactose IC50 ratio (JC-1 IC50 in glucose, JC-1 IC50 in galactose, JC-1 glu/gla, ATP IC50 in glucose, ATP IC50 in galactose, ATP glu/gla ) |
50 |
Nortriptyline |
62.0 ± 18.7, 57.8 ± 28.3, 1.1, 65.3 ± 25.0, 49.2 ± 23.0, 1.3 |
4hr |
|
H9c2 cells |
high-glucose–galactose cell viability assay with JC-1 mitochondrial membrane potential and ATP-depletion assays (CellTiter-Glo reagent ). |
|
Positive |
glucose/galactose IC50 ratio (JC-1 IC50 in glucose, JC-1 IC50 in galactose, JC-1 glu/gla, ATP IC50 in glucose, ATP IC50 in galactose, ATP glu/gla ) |
50 |
paroxetine |
37.5 ± 15.9, 36.9 ± 27.9, 1, 37.1 ± 11.3, 32.3 ± 17.8, 1.2 |
4hr |
|
H9c2 cells |
high-glucose–galactose cell viability assay with JC-1 mitochondrial membrane potential and ATP-depletion assays (CellTiter-Glo reagent ). |
|
Positive |
glucose/galactose IC50 ratio (JC-1 IC50 in glucose, JC-1 IC50 in galactose, JC-1 glu/gla, ATP IC50 in glucose, ATP IC50 in galactose, ATP glu/gla ) |
50 |
sertraline |
30.7 ± 4.7, 24.7 ± 16.0, 1.2, 29.1 ± 12.0, 23.6 ± 19.2, 1.2 |
4hr |
|
H9c2 cells |
high-glucose–galactose cell viability assay with JC-1 mitochondrial membrane potential and ATP-depletion assays (CellTiter-Glo reagent ). |
|
Positive |
glucose/galactose IC50 ratio (JC-1 IC50 in glucose, JC-1 IC50 in galactose, JC-1 glu/gla, ATP IC50 in glucose, ATP IC50 in galactose, ATP glu/gla ) |
50 |
Tamoxifen |
97.9 ± 28.0, 64.4 ± 11.4, 1.5, 75.2 ± 8.4, 43.9 ± 7.8, 1.7 |
4hr |
|
H9c2 cells |
high-glucose–galactose cell viability assay with JC-1 mitochondrial membrane potential and ATP-depletion assays (CellTiter-Glo reagent ). |
|
Positive |
glucose/galactose IC50 ratio (JC-1 IC50 in glucose, JC-1 IC50 in galactose, JC-1 glu/gla, ATP IC50 in glucose, ATP IC50 in galactose, ATP glu/gla ) |
50 |
Thioridazine |
31.0 ± 5.9, 27.7 ± 19.8 ,1.4, 24.4 ± 5.7, 21.9 ± 18.0, 1.6 |
4hr |
|
H9c2 cells |
high-glucose–galactose cell viability assay with JC-1 mitochondrial membrane potential and ATP-depletion assays (CellTiter-Glo reagent ). |
|
Positive |
glucose/galactose IC50 ratio (JC-1 IC50 in glucose, JC-1 IC50 in galactose, JC-1 glu/gla, ATP IC50 in glucose, ATP IC50 in galactose, ATP glu/gla ) |
50 |
Flutamide |
300.0 ± 0, 78.3 ± 24.8, 4.1, 266 ± 58.9 , 62.6 ± 27.3, 5 |
24hr |
|
H9c2 cells |
high-glucose–galactose cell viability assay with JC-1 mitochondrial membrane potential and ATP-depletion assays (CellTiter-Glo reagent ). |
|
Positive |
glucose/galactose IC50 ratio (JC-1 IC50 in glucose, JC-1 IC50 in galactose, JC-1 glu/gla, ATP IC50 in glucose, ATP IC50 in galactose, ATP glu/gla ) |
50 |
Nilutamide |
250 ± 86.6, 44.0 ± 12.0 , 5.7 , 300.0 ± 0, 15.6 ± 9.9 , 19.2 |
24hr |
|
H9c2 cells |
high-glucose–galactose cell viability assay with JC-1 mitochondrial membrane potential and ATP-depletion assays (CellTiter-Glo reagent ). |
|
Positive |
glucose/galactose IC50 ratio (JC-1 IC50 in glucose, JC-1 IC50 in galactose, JC-1 glu/gla, ATP IC50 in glucose, ATP IC50 in galactose, ATP glu/gla ) |
50 |
Troglitazone |
300.00 ± 0 , 1.4 ± 0.1, 219.8, 300.0 ± 0, 1.9 ± 0.1, 156.7 |
24hr |
|
H9c2 cells |
high-glucose–galactose cell viability assay with JC-1 mitochondrial membrane potential and ATP-depletion assays (CellTiter-Glo reagent ). |
|
Positive |
glucose/galactose IC50 ratio (JC-1 IC50 in glucose, JC-1 IC50 in galactose, JC-1 glu/gla, ATP IC50 in glucose, ATP IC50 in galactose, ATP glu/gla ) |
50 |
zoniporide |
300.00 ± 0, 22.1 ± 14.3, 13.6, 300.0 ± 0, 21.6 ± 5.1, 13.9 |
24hr |
|
H9c2 cells |
high-glucose–galactose cell viability assay with JC-1 mitochondrial membrane potential and ATP-depletion assays (CellTiter-Glo reagent ). |
|
Positive |
glucose/galactose IC50 ratio (JC-1 IC50 in glucose, JC-1 IC50 in galactose, JC-1 glu/gla, ATP IC50 in glucose, ATP IC50 in galactose, ATP glu/gla ) |
50 |
Antimycin A |
5.9 (42.1nM/7.1nM) |
24hr |
|
L6 |
ATP levels in high-glucose (25 mM) or galactose (10 mM) medium |
|
Positive |
glucose/galactose IC50 ratio |
325 |
Antimycin A |
10.7 (176.5nM/16.5nM) |
24hr |
|
H9c2 |
ATP levels in high-glucose (25 mM) or galactose (10 mM) medium |
|
Positive |
glucose/galactose IC50 ratio |
325 |
Antimycin A |
17.7(58.1nM/3.3nM) |
24hr |
|
HepG2 |
ATP levels in high-glucose (25 mM) or galactose (10 mM) medium |
|
Positive |
glucose/galactose IC50 ratio |
325 |
1-Octylguanidine |
4.3 |
|
|
LUHMES (Lund human mesencephalic) cells |
Glc–Gal–NeuriTox assay |
|
Positive |
EC25(NA) [Glc/Gal] |
326 |
3-NPA |
|
|
|
permeabilized LUHMES cells |
Assessment of the function of individual mitochondrial complexes using Agilent Seahorse XFe24 |
|
Positive |
EC25(NA) [Glc/Gal] |
326 |
Antimycin A |
12000 |
|
|
LUHMES (Lund human mesencephalic) cells |
Glc–Gal–NeuriTox assay |
|
Positive |
EC25(NA) [Glc/Gal] |
326 |
azoxystrobin |
3.6 |
|
|
LUHMES (Lund human mesencephalic) cells |
Glc–Gal–NeuriTox assay |
|
Positive |
EC25(NA) [Glc/Gal] |
326 |
Berberine |
7 |
|
|
LUHMES (Lund human mesencephalic) cells |
Glc–Gal–NeuriTox assay |
|
Positive |
EC25(NA) [Glc/Gal] |
326 |
Carboxin |
3.1 |
|
|
LUHMES (Lund human mesencephalic) cells |
Glc–Gal–NeuriTox assay |
|
Positive |
EC25(NA) [Glc/Gal] |
326 |
Deguelin |
450 |
|
|
LUHMES (Lund human mesencephalic) cells |
Glc–Gal–NeuriTox assay |
|
Positive |
EC25(NA) [Glc/Gal] |
326 |
fenamidone |
16 |
|
|
LUHMES (Lund human mesencephalic) cells |
Glc–Gal–NeuriTox assay |
|
Positive |
EC25(NA) [Glc/Gal] |
326 |
fenazaquin |
450 |
|
|
LUHMES (Lund human mesencephalic) cells |
Glc–Gal–NeuriTox assay |
|
Positive |
EC25(NA) [Glc/Gal] |
326 |
Fenpyroximate |
5600 |
|
|
LUHMES (Lund human mesencephalic) cells |
Glc–Gal–NeuriTox assay |
|
Positive |
EC25(NA) [Glc/Gal] |
326 |
Methyltriphenylphosphonium bromide |
8.6 |
|
|
LUHMES (Lund human mesencephalic) cells |
Glc–Gal–NeuriTox assay |
|
Positive |
EC25(NA) [Glc/Gal] |
326 |
MPP |
30 |
|
|
LUHMES (Lund human mesencephalic) cells |
Glc–Gal–NeuriTox assay |
|
Positive |
EC25(NA) [Glc/Gal] |
326 |
Nefazodone |
10 |
|
|
LUHMES (Lund human mesencephalic) cells |
Glc–Gal–NeuriTox assay |
|
Positive |
EC25(NA) [Glc/Gal] |
326 |
Oligomycin |
8.7 |
|
|
LUHMES (Lund human mesencephalic) cells |
Glc–Gal–NeuriTox assay |
|
Positive |
EC25(NA) [Glc/Gal] |
326 |
Phenformin |
27 |
|
|
LUHMES (Lund human mesencephalic) cells |
Glc–Gal–NeuriTox assay |
|
Positive |
EC25(NA) [Glc/Gal] |
326 |
picoxystrobin |
50µM |
|
|
permeabilized LUHMES cells |
Assessment of the function of individual mitochondrial complexes using Agilent Seahorse XFe24 |
|
Positive |
|
326 |
pyraclostrobin |
50µM |
|
|
permeabilized LUHMES cells |
Assessment of the function of individual mitochondrial complexes using Agilent Seahorse XFe24 |
|
Positive |
|
326 |
Pyridaben |
75000 |
|
|
LUHMES (Lund human mesencephalic) cells |
Glc–Gal–NeuriTox assay |
|
Positive |
EC25(NA) [Glc/Gal] |
326 |
Pyrimidifen |
10000 |
|
|
LUHMES (Lund human mesencephalic) cells |
Glc–Gal–NeuriTox assay |
|
Positive |
EC25(NA) [Glc/Gal] |
326 |
Rotenone |
51 |
|
|
LUHMES (Lund human mesencephalic) cells |
Glc–Gal–NeuriTox assay |
|
Positive |
EC25(NA) [Glc/Gal] |
326 |
Salinomycin |
3.7 |
|
|
LUHMES (Lund human mesencephalic) cells |
Glc–Gal–NeuriTox assay |
|
Positive |
EC25(NA) [Glc/Gal] |
326 |
Sodium Azide |
11 |
|
|
LUHMES (Lund human mesencephalic) cells |
Glc–Gal–NeuriTox assay |
|
Positive |
EC25(NA) [Glc/Gal] |
326 |
Cyanide |
5.2 |
|
|
LUHMES (Lund human mesencephalic) cells |
Glc–Gal–NeuriTox assay |
|
Positive |
EC25(NA) [Glc/Gal] |
326 |
Tebufenpyrad |
2700 |
|
|
LUHMES (Lund human mesencephalic) cells |
Glc–Gal–NeuriTox assay |
|
Positive |
EC25(NA) [Glc/Gal] |
326 |
Troglitazone |
50 μM |
|
male CD-1 mice |
isolated liver mitochondria |
Assessment of mitochondrial Ca2+ efflux with arsenazo III at 675/685 nm. |
decrease |
Positive |
|
331 |
Ciglitazone |
50 μM |
|
male CD-1 mice |
isolated liver mitochondria |
Assessment of mitochondrial Ca2+ efflux with arsenazo III at 675/685 nm. |
decrease |
Positive |
|
331 |
Troglitazone |
10-50 μM |
|
ZDF fa/fa rat & ZDF lean rat |
isolated liver mitochondria |
OCR and measured using a fluorescent oxygen probe (Presens) |
decrease |
Positive |
significantly different from control (p < 0.05) |
225 |
Pioglitazone |
25-50 μM |
|
ZDF fa/fa rat & ZDF lean rat |
isolated liver mitochondria |
OCR and measured using a fluorescent oxygen probe (Presens) |
decrease |
Positive |
significantly different from control (p < 0.05) |
225 |
Troglitazone |
10 µM |
|
ZDF fa/fa rat vs ZDF lean rat |
isolated mitochondria |
Measurement of reduced/oxidized glutathione (GSH/GSSG): the reduced/oxidized glutathione (GSH/GSSG) concentration of the samples was determined from a standard curve using the enzymatic method and a Multiskan JX system. |
lower |
Positive |
significantly different from ZDF lean rats (p < 0.05). |
225 |
Troglitazone |
10 µM |
|
ZDF fa/fa rat vs ZDF lean rat |
isolated mitochondria |
Oxidation of mitochondrial phospholipids was measured by HPLC analysis. Peak area ratio (235/206 nm) shows relative peroxidative phospholipid content. Peak areas at 206 nm and 235 nm analyze non-peroxidative and peroxidative phospholipid. |
peroxidation |
Positive |
significantly different from ZDF lean rats (p < 0.05) |
225 |
Troglitazone |
>25 µM |
1 and 2 hr |
|
HepG2 cells |
Cellular ATP concentrations were measured with a ATP Bioluminescent Somatic Cell Assay Kit |
decrease |
Positive |
|
332 |
TDGA |
0.31 |
|
Wistar rat |
hepatocytes |
ketone bodies (KB = β-hydroxybutyrate + acetoacetate) were determined with a commercially available kit (Autokit 3-HB from Wako) |
inhibition |
Positive |
IC50 (μM) |
333 |
POCA |
59.7 |
|
Wistar rat |
hepatocytes |
ketone bodies (KB = β-hydroxybutyrate + acetoacetate) were determined with a commercially available kit (Autokit 3-HB from Wako) |
inhibition |
Positive |
IC50 (μM) |
333 |
Etomoxir |
2.76 |
|
Wistar rat |
hepatocytes |
ketone bodies (KB = β-hydroxybutyrate + acetoacetate) were determined with a commercially available kit (Autokit 3-HB from Wako) |
inhibition |
Positive |
IC50 (μM) |
333 |
DET |
5.6 |
|
Wistar rat |
hepatocytes |
ketone bodies (KB = β-hydroxybutyrate + acetoacetate) were determined with a commercially available kit (Autokit 3-HB from Wako) |
inhibition |
Positive |
IC50 (μM) |
333 |
aminocarnitine |
0.97 |
|
Wistar rat |
hepatocytes |
ketone bodies (KB = β-hydroxybutyrate + acetoacetate) were determined with a commercially available kit (Autokit 3-HB from Wako) |
inhibition |
Positive |
IC50 (μM) |
333 |
palmitoylaminocarnitine |
0.11 |
|
Wistar rat |
hepatocytes |
ketone bodies (KB = β-hydroxybutyrate + acetoacetate) were determined with a commercially available kit (Autokit 3-HB from Wako) |
inhibition |
Positive |
IC50 (μM) |
333 |
ST1326 |
1.1 |
|
Wistar rat |
hepatocytes |
ketone bodies (KB = β-hydroxybutyrate + acetoacetate) were determined with a commercially available kit (Autokit 3-HB from Wako) |
inhibition |
Positive |
IC50 (μM) |
333 |
ST2425 |
0.21 |
|
Wistar rat |
hepatocytes |
ketone bodies (KB = β-hydroxybutyrate + acetoacetate) were determined with a commercially available kit (Autokit 3-HB from Wako) |
inhibition |
Positive |
IC50 (μM) |
333 |
Trimetazidine |
47.1 |
|
Wistar rat |
hepatocytes |
ketone bodies (KB = β-hydroxybutyrate + acetoacetate) were determined with a commercially available kit (Autokit 3-HB from Wako) |
inhibition |
Positive |
IC50 (μM) |
333 |
Perhexiline |
14.8 |
|
Wistar rat |
hepatocytes |
ketone bodies (KB = β-hydroxybutyrate + acetoacetate) were determined with a commercially available kit (Autokit 3-HB from Wako) |
inhibition |
Positive |
IC50 (μM) |
333 |
Amiodarone |
16.6 |
|
Wistar rat |
hepatocytes |
ketone bodies (KB = β-hydroxybutyrate + acetoacetate) were determined with a commercially available kit (Autokit 3-HB from Wako) |
inhibition |
Positive |
IC50 (μM) |
333 |
Oxfenicine |
>100 |
|
Wistar rat |
hepatocytes |
ketone bodies (KB = β-hydroxybutyrate + acetoacetate) were determined with a commercially available kit (Autokit 3-HB from Wako) |
inhibition |
Positive |
IC50 (μM) |
333 |
oxfenicine metabolite |
25.8 |
|
Wistar rat |
hepatocytes |
ketone bodies (KB = β-hydroxybutyrate + acetoacetate) were determined with a commercially available kit (Autokit 3-HB from Wako) |
inhibition |
Positive |
IC50 (μM) |
333 |
RO-25-0187 |
1.5 |
|
Wistar rat |
hepatocytes |
ketone bodies (KB = β-hydroxybutyrate + acetoacetate) were determined with a commercially available kit (Autokit 3-HB from Wako) |
inhibition |
Positive |
IC50 (μM) |
333 |
TDGA |
<0.05/0.04 |
|
human/rat |
hepatocytes |
Fatty acid oxidation (FAO) was determined by measuring 14CO2 release from 14C-labeled palmitate |
inhibition |
Positive |
IC50 (μM) |
333 |
POCA |
10.4/95.9 |
|
human/rat |
hepatocytes |
Fatty acid oxidation (FAO) was determined by measuring 14CO2 release from 14C-labeled palmitate |
inhibition |
Positive |
IC50 (μM) |
333 |
Etomoxir |
0.29/0.34 |
|
human/rat |
hepatocytes |
Fatty acid oxidation (FAO) was determined by measuring 14CO2 release from 14C-labeled palmitate |
inhibition |
Positive |
IC50 (μM) |
333 |
DET |
1.8/4.4 |
|
human/rat |
hepatocytes |
Fatty acid oxidation (FAO) was determined by measuring 14CO2 release from 14C-labeled palmitate |
inhibition |
Positive |
IC50 (μM) |
333 |
aminocarnitine |
−/− |
|
human/rat |
hepatocytes |
Fatty acid oxidation (FAO) was determined by measuring 14CO2 release from 14C-labeled palmitate |
inhibition |
Positive |
IC50 (μM) |
333 |
palmitoylaminocarnitine |
2.8/0.27 |
|
human/rat |
hepatocytes |
Fatty acid oxidation (FAO) was determined by measuring 14CO2 release from 14C-labeled palmitate |
inhibition |
Positive |
IC50 (μM) |
333 |
ST1326 |
4.0/0.98 |
|
human/rat |
hepatocytes |
Fatty acid oxidation (FAO) was determined by measuring 14CO2 release from 14C-labeled palmitate |
inhibition |
Positive |
IC50 (μM) |
333 |
ST2425 |
0.73/0.03 |
|
human/rat |
hepatocytes |
Fatty acid oxidation (FAO) was determined by measuring 14CO2 release from 14C-labeled palmitate |
inhibition |
Positive |
IC50 (μM) |
333 |
Trimetazidine |
20.5/>100 |
|
human/rat |
hepatocytes |
Fatty acid oxidation (FAO) was determined by measuring 14CO2 release from 14C-labeled palmitate |
inhibition |
Positive |
IC50 (μM) |
333 |
Perhexiline |
22.4/21.4 |
|
human/rat |
hepatocytes |
Fatty acid oxidation (FAO) was determined by measuring 14CO2 release from 14C-labeled palmitate |
inhibition |
Positive |
IC50 (μM) |
333 |
Amiodarone |
28.5/>100 |
|
human/rat |
hepatocytes |
Fatty acid oxidation (FAO) was determined by measuring 14CO2 release from 14C-labeled palmitate |
inhibition |
Positive |
IC50 (μM) |
333 |
Oxfenicine |
>100/>100 |
|
human/rat |
hepatocytes |
Fatty acid oxidation (FAO) was determined by measuring 14CO2 release from 14C-labeled palmitate |
inhibition |
Positive |
IC50 (μM) |
333 |
oxfenicine metabolite |
33.3/>100 |
|
human/rat |
hepatocytes |
Fatty acid oxidation (FAO) was determined by measuring 14CO2 release from 14C-labeled palmitate |
inhibition |
Positive |
IC50 (μM) |
333 |
RO-25-0187 |
25.5/>100 |
|
human/rat |
hepatocytes |
Fatty acid oxidation (FAO) was determined by measuring 14CO2 release from 14C-labeled palmitate |
inhibition |
Positive |
IC50 (μM) |
333 |
Cadmium |
4 |
4hr |
|
HPNE cell (human pancreatic Nestin-expressing cells) |
Mitochondrial toxicity: exposure to various concentrations of CdCl2 in the presence of 25 mM glucose or 10 mM galactose, followed by MTT assay |
increase |
Positive |
IC50_glucose/IC50_galactose |
334 |