Inhibitors | Comment | Organism | Structure |
---|---|---|---|
(4-Benzenesulfonyl-piperazin-1-yl)-(3,4,5,6-tetrahydro-2H-[1,4']bipyridinyl-4-yl)-methanone | IC50: 143 nM | Homo sapiens | |
(4-Benzenesulfonyl-piperazin-1-yl)-(3,4,5,6-tetrahydro-2H-[1,4']bipyridinyl-4-yl)-methanone | IC50: 326 nM | Rattus norvegicus | |
1-(2-methyl-4-pyrimidinyl)-4-(1-(4-bromophenylsulfonyl)piperazin-4-ylcarbonyl)piperidine | IC50: 112 nM | Homo sapiens | |
1-(2-methyl-4-pyrimidinyl)-4-(1-(4-bromophenylsulfonyl)piperazin-4-ylcarbonyl)piperidine | 76% inhibition at 0.001 mM, IC50: 398 nM | Rattus norvegicus | |
1-(2-oxazolinyl)-4-(1-(4-bromophenylsulfonyl)piperazin-4-ylcarbonyl)piperidine | 87% inhibition at 0.001 mM | Rattus norvegicus | |
1-(2-pyrimidinyl)-4-(1-(4-bromophenylsulfonyl)piperazin-4-ylcarbonyl)piperidine | 8% inhibition at 0.001 mM | Rattus norvegicus | |
1-(2-thiazolinyl)-4-(1-(4-bromophenylsulfonyl)piperazin-4-ylcarbonyl)piperidine | complete inhibition at 0.001 mM | Rattus norvegicus | |
1-(4-iodophenylsulfonyl)-4-(1-(4-pyridyl)piperidon-4-ylcarbonyl)piperazine | IC50: 82 nM | Rattus norvegicus | |
1-(4-pyrimidinyl)-4-(1-(4-bromophenylsulfonyl)piperazin-4-ylcarbonyl)piperidine | IC50: 37 nM | Homo sapiens | |
1-(4-pyrimidinyl)-4-(1-(4-bromophenylsulfonyl)piperazin-4-ylcarbonyl)piperidine | complete inhibition at 0.001 mM, IC50: 116 nM | Rattus norvegicus | |
4-(4-bromobenzoyl)-1-(1-(4-pyridyl)piperidin-4-ylcarbonyl)piperazine | 96% inhibition at 0.001 mM | Rattus norvegicus | |
4-(4-bromophenylmethyl)-1-(1-(4-pyridyl)piperidin-4-ylcarbonyl)piperazine | complete inhibition at 0.001 mM | Rattus norvegicus | |
[4-(4-Bromo-benzenesulfonyl)-piperazin-1-yl]-(3,4,5,6-tetrahydro-2H-[1,4']bipyridinyl-4-yl)-methanone | IC50: 161 nM | Homo sapiens | |
[4-(4-Bromo-benzenesulfonyl)-piperazin-1-yl]-(3,4,5,6-tetrahydro-2H-[1,4']bipyridinyl-4-yl)-methanone | IC50: 228 nM | Rattus norvegicus | |
{4-[4-(4,5-Dihydro-oxazol-2-yl)-benzylidene]-piperidin-1-yl}-(4-trifluoromethyl-phenyl)-methanone | IC50: 90 nM, complete inhibition at 0.001 nM | Rattus norvegicus |
Localization | Comment | Organism | GeneOntology No. | Textmining |
---|---|---|---|---|
microsome | - |
Rattus norvegicus | - |
- |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Homo sapiens | - |
- |
- |
Rattus norvegicus | - |
- |
- |
Synonyms | Comment | Organism |
---|---|---|
OSC | - |
Homo sapiens |
OSC | - |
Rattus norvegicus |
IC50 Value | IC50 Value Maximum | Comment | Organism | Inhibitor | Structure |
---|---|---|---|---|---|
0.000037 | - |
IC50: 37 nM | Homo sapiens | 1-(4-pyrimidinyl)-4-(1-(4-bromophenylsulfonyl)piperazin-4-ylcarbonyl)piperidine | |
0.000082 | - |
IC50: 82 nM | Rattus norvegicus | 1-(4-iodophenylsulfonyl)-4-(1-(4-pyridyl)piperidon-4-ylcarbonyl)piperazine | |
0.00009 | - |
IC50: 90 nM, complete inhibition at 0.001 nM | Rattus norvegicus | {4-[4-(4,5-Dihydro-oxazol-2-yl)-benzylidene]-piperidin-1-yl}-(4-trifluoromethyl-phenyl)-methanone | |
0.000112 | - |
IC50: 112 nM | Homo sapiens | 1-(2-methyl-4-pyrimidinyl)-4-(1-(4-bromophenylsulfonyl)piperazin-4-ylcarbonyl)piperidine | |
0.000116 | - |
complete inhibition at 0.001 mM, IC50: 116 nM | Rattus norvegicus | 1-(4-pyrimidinyl)-4-(1-(4-bromophenylsulfonyl)piperazin-4-ylcarbonyl)piperidine | |
0.000143 | - |
IC50: 143 nM | Homo sapiens | (4-Benzenesulfonyl-piperazin-1-yl)-(3,4,5,6-tetrahydro-2H-[1,4']bipyridinyl-4-yl)-methanone | |
0.000161 | - |
IC50: 161 nM | Homo sapiens | [4-(4-Bromo-benzenesulfonyl)-piperazin-1-yl]-(3,4,5,6-tetrahydro-2H-[1,4']bipyridinyl-4-yl)-methanone | |
0.000228 | - |
IC50: 228 nM | Rattus norvegicus | [4-(4-Bromo-benzenesulfonyl)-piperazin-1-yl]-(3,4,5,6-tetrahydro-2H-[1,4']bipyridinyl-4-yl)-methanone | |
0.000326 | - |
IC50: 326 nM | Rattus norvegicus | (4-Benzenesulfonyl-piperazin-1-yl)-(3,4,5,6-tetrahydro-2H-[1,4']bipyridinyl-4-yl)-methanone | |
0.000398 | - |
76% inhibition at 0.001 mM, IC50: 398 nM | Rattus norvegicus | 1-(2-methyl-4-pyrimidinyl)-4-(1-(4-bromophenylsulfonyl)piperazin-4-ylcarbonyl)piperidine |