Inhibitors | Comment | Organism | Structure |
---|---|---|---|
(2E)-2-cyano-3-hydroxy-N-[4-(trifluoromethyl)phenyl]but-2-enamide | 50% inhibition at 0.000435 mM | Homo sapiens | |
2-(4'-tert-butyl-2-chloro-biphenyl-4-ylcarbamoyl)-cyclopent-1-enecarboxylic acid | 50% inhibition at 0.000080 mM | Homo sapiens | |
2-([[2,3,5,6-tetrafluoro-3'-(trifluoromethoxy)biphenyl-4-yl]amino]carbonyl)cyclopent-1-ene-1-carboxylic acid | 50% inhibition at 0.000007 mM | Homo sapiens | |
2-([[2-chloro-3'-(trifluoromethoxy)biphenyl-4-yl]amino]carbonyl)cyclopent-1-ene-1-carboxylic acid | 50% inhibition at 0.000020 mM | Homo sapiens | |
2-([[2-chloro-4'-(dimethylamino)biphenyl-4-yl]amino]carbonyl)cyclopent-1-ene-1-carboxylic acid | 50% inhibition at 0.00005 mM | Homo sapiens | |
2-([[3'-(trifluoromethoxy)-3-(trifluoromethyl)biphenyl-4-yl]amino]carbonyl)cyclopent-1-ene-1-carboxylic acid | 50% inhibition at 0.000840 mM | Homo sapiens | |
2-([[3,5-difluoro-3'-(trifluoromethoxy)biphenyl-4-yl]amino]carbonyl)cyclopent-1-ene-1-carboxylic acid | 50% inhibition at 0.000033 mM | Homo sapiens | |
2-([[3-chloro-3'-(trifluoromethoxy)biphenyl-4-yl]amino]carbonyl)cyclopent-1-ene-1-carboxylic acid | 50% inhibition at 0.000290 mM | Homo sapiens | |
2-([[3-cyano-3'-(trifluoromethoxy)biphenyl-4-yl]amino]carbonyl)cyclopent-1-ene-1-carboxylic acid | 50% inhibition at 0.000370 mM | Homo sapiens | |
2-([[3-fluoro-3'-(trifluoromethoxy)biphenyl-4-yl]amino]carbonyl)cyclopent-1-ene-1-carboxylic acid | 50% inhibition at 0.00028 mM | Homo sapiens | |
2-([[3-fluoro-4'-(trifluoromethoxy)biphenyl-4-yl]amino]carbonyl)cyclopent-1-ene-1-carboxylic acid | 50% inhibition at 0.00570 mM | Homo sapiens | |
2-([[3-methyl-3'-(trifluoromethoxy)biphenyl-4-yl]amino]carbonyl)cyclopent-1-ene-1-carboxylic acid | 50% inhibition at 0.000150 mM | Homo sapiens | |
2-([[3-nitro-3'-(trifluoromethoxy)biphenyl-4-yl]amino]carbonyl)cyclopent-1-ene-1-carboxylic acid | 50% inhibition at 0.000390 mM | Homo sapiens | |
2-([[4'-(dimethylamino)-3,5-difluorobiphenyl-4-yl]amino]carbonyl)cyclopent-1-ene-1-carboxylic acid | 50% inhibition at 0.00061 mM | Homo sapiens | |
2-([[4-(1-naphthyl)-2-(trifluoromethyl)phenyl]amino]carbonyl)cyclopent-1-ene-1-carboxylic acid | 50% inhibition at 0.000180 mM | Homo sapiens | |
2-[(biphenyl-4-ylamino)carbonyl]cyclopent-1-ene-1-carboxylic acid | 50% inhibition at 0.00041 mM | Homo sapiens | |
2-[[(2',3,5-trifluorobiphenyl-4-yl)amino]carbonyl]cyclopent-1-ene-1-carboxylic acid | 50% inhibition at 0.000045 mM | Homo sapiens | |
2-[[(2'-chloro-3,5-difluorobiphenyl-4-yl)amino]carbonyl]cyclopent-1-ene-1-carboxylic acid | 50% inhibition at 0.000018 mM | Homo sapiens | |
2-[[(2'-chlorobiphenyl-4-yl)amino]carbonyl]cyclopent-1-ene-1-carboxylic acid | 50% inhibition at 0.000225 mM | Homo sapiens | |
2-[[(2,3,5,6-tetrafluoro-2'-methoxybiphenyl-4-yl)amino]carbonyl]cyclopent-1-ene-1-carboxylic acid | 50% inhibition at 0.000008 mM | Homo sapiens | |
2-[[(3'-ethoxy-3,5-difluorobiphenyl-4-yl)amino]carbonyl]cyclopent-1-ene-1-carboxylic acid | 50% inhibition at 0.000017 mM | Homo sapiens | |
2-[[(3,3'-dimethoxybiphenyl-4-yl)amino]carbonyl]cyclopent-1-ene-1-carboxylic acid | 50% inhibition at 0.000170 mM | Homo sapiens | |
2-[[(3,5-difluoro-2',4'-dimethoxybiphenyl-4-yl)amino]carbonyl]cyclopent-1-ene-1-carboxylic acid | 50% inhibition at 0.000090 mM | Homo sapiens | |
2-[[(3,5-difluoro-2'-methoxybiphenyl-4-yl)amino]carbonyl]cyclopent-1-ene-1-carboxylic acid | 50% inhibition at 0.000042 mM | Homo sapiens | |
2-[[(3-chloro-2'-methoxybiphenyl-4-yl)amino]carbonyl]cyclopent-1-ene-1-carboxylic acid | 50% inhibition at 0.000310 mM | Homo sapiens | |
2-[[(3-chloro-4'-methoxybiphenyl-4-yl)amino]carbonyl]cyclopent-1-ene-1-carboxylic acid | 50% inhibition at 0.00840 mM | Homo sapiens | |
2-[[(3-fluoro-3'-hydroxybiphenyl-4-yl)amino]carbonyl]cyclopent-1-ene-1-carboxylic acid | 50% inhibition at 0.000610 mM | Homo sapiens | |
2-[[(3-fluoro-4'-methoxybiphenyl-4-yl)amino]carbonyl]cyclopent-1-ene-1-carboxylic acid | 50% inhibition at 0.00170 mM | Homo sapiens | |
2-[[(4'-bromo-2-chlorobiphenyl-4-yl)amino]carbonyl]cyclopent-1-ene-1-carboxylic acid | 50% inhibition at 0.000070 mM | Homo sapiens | |
2-[[(4'-bromo-3-chlorobiphenyl-4-yl)amino]carbonyl]cyclopent-1-ene-1-carboxylic acid | 50% inhibition at 0.002900 mM | Homo sapiens | |
2-[[(4'-bromo-3-fluorobiphenyl-4-yl)amino]carbonyl]cyclopent-1-ene-1-carboxylic acid | 50% inhibition at 0.000735 mM | Homo sapiens |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Homo sapiens | - |
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