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Literature summary for 1.3.5.2 extracted from

  • Leban, J.; Saeb, W.; Garcia, G.; Baumgartner, R.; Kramer, B.
    Discovery of a novel series of DHODH inhibitors by a docking procedure and QSAR refinement (2004), Bioorg. Med. Chem. Lett., 14, 55-58.
    View publication on PubMed

Inhibitors

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

Organism UniProt Comment Textmining
Homo sapiens
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