Inhibitors | Comment | Organism | Structure |
---|---|---|---|
3-[(Z)-2,3-dihydro-1H-inden-1-ylidenemethyl]pyridine | 50% inhibition at 0.087 mM | Homo sapiens | |
4-[(Z)-(5-fluoro-2,3-dihydro-1H-inden-1-ylidene)methyl]pyridine | 50% inhibition at 0.034 mM, selective for CYP11B1 | Homo sapiens | |
5-[(1E)-1-(5-fluoro-2,3-dihydro-1H-inden-1-ylidene)ethyl]isoquinoline | 50% inhibition at 0.096 mM | Homo sapiens | |
5-[(E)-(5-fluoro-2,3-dihydro-1H-inden-1-ylidene)methyl]isoquinoline | 50% inhibition at 0.058 mM, selective for CYP11B1 | Homo sapiens | |
5-[(E)-(5-fluoro-2,3-dihydro-1H-inden-1-ylidene)methyl]pyrimidine | 50% inhibition at 0.027 mM, very selective for CYP11B1 | Homo sapiens | |
5-[(Z)-(5-fluoro-2,3-dihydro-1H-inden-1-ylidene)methyl]isoquinoline | 50% inhibition at 0.026 mM, selective for CYP11B1 | Homo sapiens | |
fadrozole | 50% inhibition at 0.001 mM | Homo sapiens | |
ketoconazole | 50% inhibition at 0.081 mM | Homo sapiens |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Homo sapiens | - |
- |
- |