Affinity DataKi: 0.00150nMAssay Description:Binding affinity against alpha thrombinMore data for this Ligand-Target Pair
Affinity DataKi: 0.00200nMAssay Description:Binding affinity against alpha thrombinMore data for this Ligand-Target Pair
Affinity DataKi: 0.00400nMAssay Description:Binding affinity against gamma thrombinMore data for this Ligand-Target Pair
Affinity DataKi: 0.00490nMAssay Description:Binding affinity against kallikreinMore data for this Ligand-Target Pair
Affinity DataKi: 0.00700nMAssay Description:Binding affinity against alpha thrombinMore data for this Ligand-Target Pair
Affinity DataKi: 0.00700nMAssay Description:Binding affinity against alpha thrombinMore data for this Ligand-Target Pair
Affinity DataKi: 0.0110nMAssay Description:Binding affinity against ChymotrypsinMore data for this Ligand-Target Pair
Affinity DataKi: 0.0110nMAssay Description:Binding affinity against gamma thrombinMore data for this Ligand-Target Pair
Affinity DataKi: 0.0180nMAssay Description:Binding affinity against alpha thrombinMore data for this Ligand-Target Pair
Affinity DataKi: 0.0190nMAssay Description:Binding affinity against alpha thrombinMore data for this Ligand-Target Pair
Affinity DataKi: 0.0190nMAssay Description:Binding affinity against gamma thrombinMore data for this Ligand-Target Pair
Affinity DataKi: 0.0210nMAssay Description:Binding affinity against ChymotrypsinMore data for this Ligand-Target Pair
Affinity DataKi: 0.0240nMAssay Description:Binding affinity against gamma thrombinMore data for this Ligand-Target Pair
Affinity DataKi: 0.0270nMAssay Description:Binding affinity against gamma thrombinMore data for this Ligand-Target Pair
Affinity DataKi: 0.0280nMAssay Description:Binding affinity against gamma thrombinMore data for this Ligand-Target Pair
Affinity DataKi: 0.0280nMAssay Description:Binding affinity against alpha thrombinMore data for this Ligand-Target Pair
Affinity DataKi: 0.0340nMAssay Description:Binding affinity against gamma thrombinMore data for this Ligand-Target Pair
Affinity DataKi: 0.0420nMAssay Description:Binding affinity against alpha thrombinMore data for this Ligand-Target Pair
Affinity DataKi: 0.0540nMAssay Description:Binding affinity against TrypsinMore data for this Ligand-Target Pair
Affinity DataKi: 0.0590nMAssay Description:Binding affinity against gamma thrombinMore data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Rattus norvegicus)
Glaxo Inc. Research Institute
Curated by ChEMBL
Glaxo Inc. Research Institute
Curated by ChEMBL
Affinity DataKi: 0.0700nMAssay Description:Inhibition of recombinant Steroid 5-alpha-reductase type I was evaluated as binding affinity (in vitro)More data for this Ligand-Target Pair
Affinity DataKi: 0.0820nMAssay Description:Binding affinity against alpha thrombinMore data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Rattus norvegicus)
Glaxo Inc. Research Institute
Curated by ChEMBL
Glaxo Inc. Research Institute
Curated by ChEMBL
Affinity DataKi: 0.100nMAssay Description:Inhibition of recombinant Steroid 5-alpha-reductase type I was evaluated as binding affinity of the compoundMore data for this Ligand-Target Pair
Affinity DataKi: 0.100nMAssay Description:Inhibition of Influenza A virus (A/Thailand/1(KAN-1)/2004(H5N1)) neuraminidase by by Michaelis Menten equation analysisMore data for this Ligand-Target Pair
Affinity DataKi: 0.115nMAssay Description:Binding affinity against ChymotrypsinMore data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Rattus norvegicus)
Glaxo Inc. Research Institute
Curated by ChEMBL
Glaxo Inc. Research Institute
Curated by ChEMBL
Affinity DataKi: 0.120nMAssay Description:Inhibitory activity was measured on rat Steroid 5-alpha-reductase type 2More data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Glaxo Inc. Research Institute
Curated by ChEMBL
Glaxo Inc. Research Institute
Curated by ChEMBL
Affinity DataKi: 0.130nMAssay Description:Binding affinity to recombinant human Steroid 5-alpha-reductase type I was evaluatedMore data for this Ligand-Target Pair
Affinity DataKi: 0.130nMAssay Description:Binding affinity against alpha thrombinMore data for this Ligand-Target Pair
Affinity DataKi: 0.140nMAssay Description:Binding affinity against gamma thrombinMore data for this Ligand-Target Pair
Affinity DataKi: 0.150nMAssay Description:Binding affinity against TrypsinMore data for this Ligand-Target Pair
Affinity DataKi: 0.152nMAssay Description:Binding affinity against ChymotrypsinMore data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Rattus norvegicus)
Glaxo Inc. Research Institute
Curated by ChEMBL
Glaxo Inc. Research Institute
Curated by ChEMBL
Affinity DataKi: 0.170nMAssay Description:Inhibitory activity was measured on rat Steroid 5-alpha-reductase type 2More data for this Ligand-Target Pair
Affinity DataKi: 0.174nMAssay Description:Binding affinity against cathepsin GMore data for this Ligand-Target Pair
Affinity DataKi: 0.187nMAssay Description:Binding affinity against cathepsin GMore data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Glaxo Inc. Research Institute
Curated by ChEMBL
Glaxo Inc. Research Institute
Curated by ChEMBL
Affinity DataKi: 0.200nMAssay Description:Inhibition of recombinant steroid 5-alpha-reductase type IMore data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Glaxo Inc. Research Institute
Curated by ChEMBL
Glaxo Inc. Research Institute
Curated by ChEMBL
Affinity DataKi: 0.200nMAssay Description:Inhibition of recombinant steroid 5-alpha-reductase type IMore data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Glaxo Inc. Research Institute
Curated by ChEMBL
Glaxo Inc. Research Institute
Curated by ChEMBL
Affinity DataKi: 0.200nMAssay Description:Inhibition of recombinant steroid 5-alpha-reductase type IMore data for this Ligand-Target Pair
Affinity DataKi: 0.230nMAssay Description:Binding affinity against adenosine A1 receptor in rat cortex by the displacement of [3H]-cyclohexyladenosine (CHA).More data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Rattus norvegicus)
Glaxo Inc. Research Institute
Curated by ChEMBL
Glaxo Inc. Research Institute
Curated by ChEMBL
Affinity DataKi: 0.270nMAssay Description:Inhibition of recombinant Steroid 5-alpha-reductase type I was evaluated as binding affinity of the compoundMore data for this Ligand-Target Pair
Affinity DataKi: 0.270nMAssay Description:Binding affinity against TrypsinMore data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Glaxo Inc. Research Institute
Curated by ChEMBL
Glaxo Inc. Research Institute
Curated by ChEMBL
Affinity DataKi: 0.300nMAssay Description:Inhibition of recombinant steroid 5-alpha-reductase type IMore data for this Ligand-Target Pair
Affinity DataKi: 0.300nMAssay Description:Binding affinity against adenosine A1 receptor in rat cortex by the displacement of [3H]-cyclohexyladenosine (CHA).More data for this Ligand-Target Pair
Affinity DataKi: 0.320nMAssay Description:Binding affinity against TrypsinMore data for this Ligand-Target Pair
TargetChymotrypsin-like elastase family member 2A(Sus scrofa)
Thrombosis Research Institute
Curated by ChEMBL
Thrombosis Research Institute
Curated by ChEMBL
Affinity DataKi: 0.365nMAssay Description:Binding affinity of the compound towards porcine pancreatic elastaseMore data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Glaxo Inc. Research Institute
Curated by ChEMBL
Glaxo Inc. Research Institute
Curated by ChEMBL
Affinity DataKi: 0.400nMAssay Description:In vitro inhibitory activity against human type 1 5-alpha reductaseMore data for this Ligand-Target Pair
Affinity DataKi: 0.400nMAssay Description:Inhibition of Influenza A virus (A/chicken/Yogjakarta/BBVet-IX/2004(H5N1)) neuraminidase by Michaelis Menten equation analysisMore data for this Ligand-Target Pair
Affinity DataKi: 0.440nMAssay Description:Binding affinity against TrypsinMore data for this Ligand-Target Pair
Affinity DataKi: 0.450nMAssay Description:Binding affinity against TrypsinMore data for this Ligand-Target Pair
Affinity DataKi: 0.5nMAssay Description:Inhibition of Influenza A virus (A/Thailand/1(KAN-1)/2004(H5N1)) neuraminidase by by Michaelis Menten equation analysisMore data for this Ligand-Target Pair
Affinity DataKi: 0.5nMAssay Description:Inhibition of Influenza A virus (A/duck/Laos/25/2006(H5N1)) neuraminidase by Michaelis Menten equation analysisMore data for this Ligand-Target Pair