Compile Data Set for Download or QSAR
Found 195 Enz. Inhib. hit(s) with all data for entry = 2710
TargetNeutrophil elastase(Homo sapiens (Human))
Montana State University

LigandPNGBDBM23698(4-chloro-1-[(4-fluorophenyl)carbonyl]-1H-pyrazole ...)copy SMILEScopy InChI
Affinity DataKi:  6nM ΔG°:  -46.9kJ/molepH: 7.5 T: 2°CAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7N5SPubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Montana State University

LigandPNGBDBM23700(N-Benzoylpyrazole deriv., 2 | methyl 1-[(4-chlorop...)copy SMILEScopy InChI
Affinity DataKi:  15nM ΔG°:  -44.7kJ/molepH: 7.5 T: 2°CAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7N5SPubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Montana State University

LigandPNGBDBM23709(3-methyl-1-[(3,4,5-trimethoxyphenyl)carbonyl]-1H-p...)copy SMILEScopy InChI
Affinity DataKi:  21nM ΔG°:  -43.8kJ/molepH: 7.5 T: 2°CAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7N5SPubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Montana State University

LigandPNGBDBM23701(4-chloro-1-[(3-nitrophenyl)carbonyl]-1H-pyrazole |...)copy SMILEScopy InChI
Affinity DataKi:  24nM ΔG°:  -43.5kJ/molepH: 7.5 T: 2°CAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7N5SPubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Montana State University

LigandPNGBDBM23702(3-[(2,4-dimethylphenyl)carbonyl]-1-[(4-fluoropheny...)copy SMILEScopy InChI
Affinity DataKi:  24nM ΔG°:  -43.5kJ/molepH: 7.5 T: 2°CAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7N5SPubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Montana State University

LigandPNGBDBM23710(1-[(4-methylphenyl)carbonyl]-3-nitro-1H-pyrazole |...)copy SMILEScopy InChI
Affinity DataKi:  28nM ΔG°:  -43.1kJ/molepH: 7.5 T: 2°CAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7N5SPubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Montana State University

LigandPNGBDBM23703(1-benzoyl-4-nitro-1H-pyrazole | N-Benzoylpyrazole ...)copy SMILEScopy InChI
Affinity DataKi:  34nM ΔG°:  -42.6kJ/molepH: 7.5 T: 2°CAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7N5SPubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Montana State University

LigandPNGBDBM23704(1-benzoyl-N-phenyl-1H-pyrazole-3-carboxamide | N-B...)copy SMILEScopy InChI
Affinity DataKi:  39nM ΔG°:  -42.3kJ/molepH: 7.5 T: 2°CAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7N5SPubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Montana State University

LigandPNGBDBM23705(4-bromo-1-[(4-methylphenyl)carbonyl]-1H-pyrazole |...)copy SMILEScopy InChI
Affinity DataKi:  45nM ΔG°:  -41.9kJ/molepH: 7.5 T: 2°CAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7N5SPubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Montana State University

LigandPNGBDBM23711(1-benzoyl-3-nitro-1H-pyrazole | N-Benzoylpyrazole ...)copy SMILEScopy InChI
Affinity DataKi:  46nM ΔG°:  -41.9kJ/molepH: 7.5 T: 2°CAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7N5SPubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Montana State University

LigandPNGBDBM23712(1-[(2-methylphenyl)carbonyl]-4-nitro-1H-pyrazole |...)copy SMILEScopy InChI
Affinity DataKi:  65nM ΔG°:  -41.0kJ/molepH: 7.5 T: 2°CAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7N5SPubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Montana State University

LigandPNGBDBM23706(1-[(3,4-dichlorophenyl)carbonyl]-1H-pyrazole | N-B...)copy SMILEScopy InChI
Affinity DataKi:  104nM ΔG°:  -39.9kJ/molepH: 7.5 T: 2°CAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7N5SPubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Montana State University

LigandPNGBDBM23707(1-[(2-fluorophenyl)carbonyl]-5-methyl-3-nitro-1H-p...)copy SMILEScopy InChI
Affinity DataKi:  107nM ΔG°:  -39.8kJ/molepH: 7.5 T: 2°CAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7N5SPubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Montana State University

LigandPNGBDBM23726(1,1-dimethylprop-2-yn-1-yl 4-methoxybenzoate, 10 |...)copy SMILEScopy InChI
Affinity DataKi:  110nM ΔG°:  -39.7kJ/molepH: 7.5 T: 2°CAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7N5SPubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Montana State University

LigandPNGBDBM23713(4-chloro-1-[(2-methylphenyl)carbonyl]-1H-pyrazole ...)copy SMILEScopy InChI
Affinity DataKi:  230nM ΔG°:  -37.9kJ/molepH: 7.5 T: 2°CAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7N5SPubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Montana State University

LigandPNGBDBM23714(4-bromo-1-[(3-methylphenyl)carbonyl]-1H-pyrazole |...)copy SMILEScopy InChI
Affinity DataKi:  250nM ΔG°:  -37.7kJ/molepH: 7.5 T: 2°CAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7N5SPubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Montana State University

LigandPNGBDBM23727(N,N-bis(cyanomethyl)-3,4-dimethoxybenzamide | N,N-...)copy SMILEScopy InChI
Affinity DataKi:  290nM ΔG°:  -37.3kJ/molepH: 7.5 T: 2°CAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7N5SPubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Montana State University

LigandPNGBDBM23716(N-Benzoylpyrazole deriv., 24 | N-{4-[(3-methyl-1H-...)copy SMILEScopy InChI
Affinity DataKi:  300nM ΔG°:  -37.2kJ/molepH: 7.5 T: 2°CAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7N5SPubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Montana State University

LigandPNGBDBM23715(4-bromo-1-[(2-methylphenyl)carbonyl]-1H-pyrazole |...)copy SMILEScopy InChI
Affinity DataKi:  300nM ΔG°:  -37.2kJ/molepH: 7.5 T: 2°CAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7N5SPubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Montana State University

LigandPNGBDBM23728(2-(2-methoxyphenoxy)-N'-(thiophen-2-ylcarbonyl)ace...)copy SMILEScopy InChI
Affinity DataKi:  820nM ΔG°:  -34.7kJ/molepH: 7.5 T: 2°CAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7N5SPubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Montana State University

LigandPNGBDBM23717(4-chloro-1-[(2-chlorophenyl)carbonyl]-1H-pyrazole ...)copy SMILEScopy InChI
Affinity DataKi:  1.00E+3nM ΔG°:  -34.2kJ/molepH: 7.5 T: 2°CAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7N5SPubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Montana State University

LigandPNGBDBM23708(4-bromo-1-[(2,6-difluorophenyl)carbonyl]-1H-pyrazo...)copy SMILEScopy InChI
Affinity DataKi:  1.10E+3nM ΔG°:  -34.0kJ/molepH: 7.5 T: 2°CAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7N5SPubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Montana State University

LigandPNGBDBM23730(1,2,4-triazole-5-carboxylate, 14 | methyl 3-[2-(1,...)copy SMILEScopy InChI
Affinity DataKi:  1.60E+3nMAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7N5SPubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Montana State University

LigandPNGBDBM23731(4-methoxy-N -(phenylacetyl)benzohydrazide | 4-meth...)copy SMILEScopy InChI
Affinity DataKi:  2.50E+3nMAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7N5SPubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Montana State University

LigandPNGBDBM23732(3-(2-chlorophenyl)-5-methyl-4-(1H-pyrazol-1-ylcarb...)copy SMILEScopy InChI
Affinity DataKi:  3.10E+3nMAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7N5SPubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Montana State University

LigandPNGBDBM23718(1-[(2-methylphenyl)carbonyl]-1H-pyrazole | N-Benzo...)copy SMILEScopy InChI
Affinity DataKi:  3.40E+3nM ΔG°:  -31.2kJ/molepH: 7.5 T: 2°CAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7N5SPubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Montana State University

LigandPNGBDBM23719(4-bromo-1-[(2-chloro-4,5-difluorophenyl)carbonyl]-...)copy SMILEScopy InChI
Affinity DataKi:  7.20E+3nM ΔG°:  -29.4kJ/molepH: 7.5 T: 2°CAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7N5SPubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Montana State University

LigandPNGBDBM23720(1-[(4-tert-butylphenyl)carbonyl]-4-chloro-1H-pyraz...)copy SMILEScopy InChI
Affinity DataKi:  9.00E+3nM ΔG°:  -28.8kJ/molepH: 7.5 T: 2°CAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7N5SPubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Montana State University

LigandPNGBDBM23721(4-chloro-1-[(2-fluorophenyl)carbonyl]-3,5-dimethyl...)copy SMILEScopy InChI
Affinity DataKi:  9.00E+3nM ΔG°:  -28.8kJ/molepH: 7.5 T: 2°CAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7N5SPubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Montana State University

LigandPNGBDBM23722(4-chloro-1-[(4-chlorophenyl)carbonyl]-3,5-dimethyl...)copy SMILEScopy InChI
Affinity DataKi:  1.07E+4nM ΔG°:  -28.4kJ/molepH: 7.5 T: 2°CAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7N5SPubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Montana State University

LigandPNGBDBM23723(4-bromo-1-[(4-methoxyphenyl)carbonyl]-3,5-dimethyl...)copy SMILEScopy InChI
Affinity DataKi:  2.45E+4nM ΔG°:  -26.3kJ/molepH: 7.5 T: 2°CAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7N5SPubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Montana State University

LigandPNGBDBM23724(1-[(2-bromophenyl)carbonyl]-1H-pyrazole | N-Benzoy...)copy SMILEScopy InChI
Affinity DataKi:  2.99E+4nM ΔG°:  -25.8kJ/molepH: 7.5 T: 2°CAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7N5SPubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Montana State University

LigandPNGBDBM23725(3,4,5-trimethyl-1-[(3,4,5-trimethoxyphenyl)carbony...)copy SMILEScopy InChI
Affinity DataKi:  5.09E+4nM ΔG°:  -24.5kJ/molepH: 7.5 T: 2°CAssay Description:HTS was performed in black flat-bottom 96-well microtiter plates. The reaction was initiated by addition of elastase substrate to the reaction buffer...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7N5SPubMed
TargetChymotrypsin-C(Homo sapiens (Human))
Montana State University

LigandPNGBDBM23705(4-bromo-1-[(4-methylphenyl)carbonyl]-1H-pyrazole |...)copy SMILEScopy InChI
Affinity DataIC50: 15nMAssay Description:Chymotrypsin activity was monitored at excitation and emission wavelengths of 355 and 460 nm, respectively. For all compounds tested, the concentrati...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7N5SPubMed
TargetChymotrypsin-C(Homo sapiens (Human))
Montana State University

LigandPNGBDBM23700(N-Benzoylpyrazole deriv., 2 | methyl 1-[(4-chlorop...)copy SMILEScopy InChI
Affinity DataIC50: 15nMAssay Description:Chymotrypsin activity was monitored at excitation and emission wavelengths of 355 and 460 nm, respectively. For all compounds tested, the concentrati...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7N5SPubMed
TargetChymotrypsin-C(Homo sapiens (Human))
Montana State University

LigandPNGBDBM23698(4-chloro-1-[(4-fluorophenyl)carbonyl]-1H-pyrazole ...)copy SMILEScopy InChI
Affinity DataIC50: 40nMAssay Description:Chymotrypsin activity was monitored at excitation and emission wavelengths of 355 and 460 nm, respectively. For all compounds tested, the concentrati...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7N5SPubMed
TargetChymotrypsin-C(Homo sapiens (Human))
Montana State University

LigandPNGBDBM23709(3-methyl-1-[(3,4,5-trimethoxyphenyl)carbonyl]-1H-p...)copy SMILEScopy InChI
Affinity DataIC50: 50nMAssay Description:Chymotrypsin activity was monitored at excitation and emission wavelengths of 355 and 460 nm, respectively. For all compounds tested, the concentrati...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7N5SPubMed
TargetProthrombin(Homo sapiens (Human))
Montana State University

LigandPNGBDBM23700(N-Benzoylpyrazole deriv., 2 | methyl 1-[(4-chlorop...)copy SMILEScopy InChI
Affinity DataIC50: 51nMAssay Description:Thrombin activity was monitored at excitation and emission wavelengths of 355 and 460 nm, respectively. For all compounds tested, the concentration o...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7N5SPubMed
TargetChymotrypsin-C(Homo sapiens (Human))
Montana State University

LigandPNGBDBM23704(1-benzoyl-N-phenyl-1H-pyrazole-3-carboxamide | N-B...)copy SMILEScopy InChI
Affinity DataIC50: 57nMAssay Description:Chymotrypsin activity was monitored at excitation and emission wavelengths of 355 and 460 nm, respectively. For all compounds tested, the concentrati...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7N5SPubMed
TargetChymotrypsin-C(Homo sapiens (Human))
Montana State University

LigandPNGBDBM23702(3-[(2,4-dimethylphenyl)carbonyl]-1-[(4-fluoropheny...)copy SMILEScopy InChI
Affinity DataIC50: 120nMAssay Description:Chymotrypsin activity was monitored at excitation and emission wavelengths of 355 and 460 nm, respectively. For all compounds tested, the concentrati...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7N5SPubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Montana State University

LigandPNGBDBM23700(N-Benzoylpyrazole deriv., 2 | methyl 1-[(4-chlorop...)copy SMILEScopy InChI
Affinity DataIC50: 120nMAssay Description:Urokinase activity was monitored at excitation and emission wavelengths of 355 and 460 nm, respectively. For all compounds tested, the concentration ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7N5SPubMed
TargetProthrombin(Homo sapiens (Human))
Montana State University

LigandPNGBDBM23702(3-[(2,4-dimethylphenyl)carbonyl]-1-[(4-fluoropheny...)copy SMILEScopy InChI
Affinity DataIC50: 120nMAssay Description:Thrombin activity was monitored at excitation and emission wavelengths of 355 and 460 nm, respectively. For all compounds tested, the concentration o...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7N5SPubMed
TargetChymotrypsin-C(Homo sapiens (Human))
Montana State University

LigandPNGBDBM23706(1-[(3,4-dichlorophenyl)carbonyl]-1H-pyrazole | N-B...)copy SMILEScopy InChI
Affinity DataIC50: 125nMAssay Description:Chymotrypsin activity was monitored at excitation and emission wavelengths of 355 and 460 nm, respectively. For all compounds tested, the concentrati...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7N5SPubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Montana State University

LigandPNGBDBM23701(4-chloro-1-[(3-nitrophenyl)carbonyl]-1H-pyrazole |...)copy SMILEScopy InChI
Affinity DataIC50: 170nMAssay Description:Urokinase activity was monitored at excitation and emission wavelengths of 355 and 460 nm, respectively. For all compounds tested, the concentration ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7N5SPubMed
TargetChymotrypsin-C(Homo sapiens (Human))
Montana State University

LigandPNGBDBM23710(1-[(4-methylphenyl)carbonyl]-3-nitro-1H-pyrazole |...)copy SMILEScopy InChI
Affinity DataIC50: 190nMAssay Description:Chymotrypsin activity was monitored at excitation and emission wavelengths of 355 and 460 nm, respectively. For all compounds tested, the concentrati...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7N5SPubMed
TargetChymotrypsin-C(Homo sapiens (Human))
Montana State University

LigandPNGBDBM23712(1-[(2-methylphenyl)carbonyl]-4-nitro-1H-pyrazole |...)copy SMILEScopy InChI
Affinity DataIC50: 240nMAssay Description:Chymotrypsin activity was monitored at excitation and emission wavelengths of 355 and 460 nm, respectively. For all compounds tested, the concentrati...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7N5SPubMed
TargetChymotrypsin-C(Homo sapiens (Human))
Montana State University

LigandPNGBDBM23701(4-chloro-1-[(3-nitrophenyl)carbonyl]-1H-pyrazole |...)copy SMILEScopy InChI
Affinity DataIC50: 340nMAssay Description:Chymotrypsin activity was monitored at excitation and emission wavelengths of 355 and 460 nm, respectively. For all compounds tested, the concentrati...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7N5SPubMed
TargetProthrombin(Homo sapiens (Human))
Montana State University

LigandPNGBDBM23704(1-benzoyl-N-phenyl-1H-pyrazole-3-carboxamide | N-B...)copy SMILEScopy InChI
Affinity DataIC50: 390nMAssay Description:Thrombin activity was monitored at excitation and emission wavelengths of 355 and 460 nm, respectively. For all compounds tested, the concentration o...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7N5SPubMed
TargetProthrombin(Homo sapiens (Human))
Montana State University

LigandPNGBDBM23701(4-chloro-1-[(3-nitrophenyl)carbonyl]-1H-pyrazole |...)copy SMILEScopy InChI
Affinity DataIC50: 680nMAssay Description:Thrombin activity was monitored at excitation and emission wavelengths of 355 and 460 nm, respectively. For all compounds tested, the concentration o...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7N5SPubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Montana State University

LigandPNGBDBM23702(3-[(2,4-dimethylphenyl)carbonyl]-1-[(4-fluoropheny...)copy SMILEScopy InChI
Affinity DataIC50: 1.10E+3nMAssay Description:Urokinase activity was monitored at excitation and emission wavelengths of 355 and 460 nm, respectively. For all compounds tested, the concentration ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ST7N5SPubMed
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