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Results 1 - 10 of 194 > >>
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EC Number Inhibitors Commentary Structure
Show all pathways known for 6.1.1.20Display the word mapDisplay the reaction diagram Show all sequences 6.1.1.20(2R,3R,3aS,5aR,10R,10aR)-N-(3,4-dichlorophenyl)-10-hydroxy-4-oxo-2-phenyl-2,3,3a,4,5a,10-hexahydrofuro[2,3-c]indeno[1,2-b]furan-3-carboxamide - Go to the Ligand Summary Page
Show all pathways known for 6.1.1.20Display the word mapDisplay the reaction diagram Show all sequences 6.1.1.20(2R,3R,3aS,5aR,10S,10aR)-N-(3,4-dichlorophenyl)-10-hydroxy-4-oxo-2-phenyl-2,3,3a,4,5a,10-hexahydrofuro[2,3-c]indeno[1,2-b]furan-3-carboxamide - Go to the Ligand Summary Page
Show all pathways known for 6.1.1.20Display the word mapDisplay the reaction diagram Show all sequences 6.1.1.20(2R,3R,3aS,5aS,10aR)-N-(3,4-dichlorophenyl)-4,10-dioxo-2-phenyl-2,3,3a,4,5a,10-hexahydrofuro[2,3-c]indeno[1,2-b]furan-3-carboxamide IC50: 0.0026 mM; IC50: 0.0031 mM Go to the Ligand Summary Page
Show all pathways known for 6.1.1.20Display the word mapDisplay the reaction diagram Show all sequences 6.1.1.20(2R,3R,3aS,5aS,10R,10aS)-N-(3,4-dichlorophenyl)-10-hydroxy-4-oxo-2-phenyl-2,3,3a,4,5a,10-hexahydrofuro[2,3-c]indeno[1,2-b]furan-3-carboxamide IC50: 0.00047 mM; IC50: 0.00051 mM Go to the Ligand Summary Page
Show all pathways known for 6.1.1.20Display the word mapDisplay the reaction diagram Show all sequences 6.1.1.20(2R,3R,3aS,5aS,10S,10aS)-N-(3,4-dichlorophenyl)-10-hydroxy-4-oxo-2-phenyl-2,3,3a,4,5a,10-hexahydrofuro[2,3-c]indeno[1,2-b]furan-3-carboxamide IC50: 0.00017 mM; IC50: 0.00026 mM Go to the Ligand Summary Page
Show all pathways known for 6.1.1.20Display the word mapDisplay the reaction diagram Show all sequences 6.1.1.20(2Z)-2-(cyclopropylimino)-3-(2-thienylmethyl)-1,3-thiazolidin-4-one competitive with respect to Phe, selective for bacterial Phe-RS versus human Phe-RS, IC50: 0.002 mM Go to the Ligand Summary Page
Show all pathways known for 6.1.1.20Display the word mapDisplay the reaction diagram Show all sequences 6.1.1.20(2Z)-2-(cyclopropylimino)-3-(2-thienylmethyl)-1,3-thiazolidin-4-one competitive with respect to Phe, selective for bacterial Phe-RS versus human Phe-RS, IC50: 0.00017 mM Go to the Ligand Summary Page
Show all pathways known for 6.1.1.20Display the word mapDisplay the reaction diagram Show all sequences 6.1.1.20(2Z)-2-(cyclopropylimino)-3-(2-thienylmethyl)-1,3-thiazolidin-4-one competitive with respect to Phe, selective for bacterial Phe-RS versus human Phe-RS, IC50: 0.0016 mM Go to the Ligand Summary Page
Show all pathways known for 6.1.1.20Display the word mapDisplay the reaction diagram Show all sequences 6.1.1.20(2Z)-2-[(3-chlorophenyl)imino]-3-(2-thienylmethyl)-1,3-thiazolidin-4-one IC50: 600 nM Go to the Ligand Summary Page
Show all pathways known for 6.1.1.20Display the word mapDisplay the reaction diagram Show all sequences 6.1.1.20(2Z)-2-[(3-chlorophenyl)imino]-3-(2-thienylmethyl)-1,3-thiazolidin-4-one IC50: 10 nM Go to the Ligand Summary Page
Results 1 - 10 of 194 > >>
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