Compile Data Set for Download or QSAR
Found 74 Enz. Inhib. hit(s) with all data for entry = 50018357
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50194745(CHEMBL385900 | diphenyl 1-[(N-2-thiophenesulfonyl-...)copy SMILEScopy InChI
Affinity DataIC50: 1.5nMAssay Description:Inhibition of human uPAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VT3PubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50194741(CHEMBL385158 | diphenyl 1-[(N-benzenesulfonyl-D-se...)copy SMILEScopy InChI
Affinity DataIC50: 2.60nMAssay Description:Inhibition of human uPAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VT3PubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50194743(CHEMBL214814 | diphenyl 1-[(N-alpha-toluenesulfony...)copy SMILEScopy InChI
Affinity DataIC50: 3.5nMAssay Description:Inhibition of human uPAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VT3PubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50145689(CHEMBL80844 | [1-[(S)-2-((R)-2-Benzyloxycarbonylam...)copy SMILEScopy InChI
Affinity DataIC50: 4.30nMAssay Description:Inhibition of human uPAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VT3PubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50194737(CHEMBL384263 | diphenyl 1-[(N-o-methylbenzoyl-D-se...)copy SMILEScopy InChI
Affinity DataIC50: 4.40nMAssay Description:Inhibition of human uPAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VT3PubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50194746(CHEMBL405546 | diphenyl 1-[(N-o-methylbenzoyl-D-se...)copy SMILEScopy InChI
Affinity DataIC50: 5nMAssay Description:Inhibition of human uPAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VT3PubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50194742(CHEMBL263977 | diphenyl 1-[(N-benzyl-D-seryl)-L-al...)copy SMILEScopy InChI
Affinity DataIC50: 5nMAssay Description:Inhibition of human uPAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VT3PubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50194744(CHEMBL385897 | diphenyl 1-[(N-naphthalenesulfonyl-...)copy SMILEScopy InChI
Affinity DataIC50: 5.80nMAssay Description:Inhibition of human uPAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VT3PubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50194734(CHEMBL386275 | diphenyl 1-[(N-p-methoxybenzenesulf...)copy SMILEScopy InChI
Affinity DataIC50: 5.80nMAssay Description:Inhibition of human uPAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VT3PubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50194736(CHEMBL189823 | diphenyl 1-[(N-o,o-dimethylbenzoyl-...)copy SMILEScopy InChI
Affinity DataIC50: 6nMAssay Description:Inhibition of human uPAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VT3PubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50194735(CHEMBL215961 | diphenyl 1-[(N-p-cyanobenzenesulfon...)copy SMILEScopy InChI
Affinity DataIC50: 6.20nMAssay Description:Inhibition of human uPAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VT3PubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50194738(CHEMBL386249 | diphenyl 1-[(N-p-bromobenzenesulfon...)copy SMILEScopy InChI
Affinity DataIC50: 6.60nMAssay Description:Inhibition of human uPAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VT3PubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50194732(CHEMBL214539 | di-(4-acetamidophenyl) 1-[(N-benzyl...)copy SMILEScopy InChI
Affinity DataIC50: 6.70nMAssay Description:Inhibition of [3H]-FPP incorporation into biotin-linked K-ras decapeptide (CVIM) by bovine farnesyltransferaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VT3PubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50194739(CHEMBL213216 | diphenyl 1-[(N-2-thienyl-D-seryl)-L...)copy SMILEScopy InChI
Affinity DataIC50: 6.90nMAssay Description:Inhibition of human uPAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VT3PubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50194740(CHEMBL404226 | diphenyl 1-[(N-p-methylbenzoyl-D-se...)copy SMILEScopy InChI
Affinity DataIC50: 7nMAssay Description:Inhibition of human uPAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VT3PubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50194733(CHEMBL411215 | diphenyl 1-[(N-1-adamantanyl-D-sery...)copy SMILEScopy InChI
Affinity DataIC50: 8nMAssay Description:Inhibition of human uPAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VT3PubMed
TargetPlasminogen(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50194743(CHEMBL214814 | diphenyl 1-[(N-alpha-toluenesulfony...)copy SMILEScopy InChI
Affinity DataIC50: 37nMAssay Description:Inhibition of human plasminMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VT3PubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50145688(CHEMBL311067 | benzyl (R)-1-((S)-1-(1-(diphenoxyph...)copy SMILEScopy InChI
Affinity DataIC50: 61nMAssay Description:Inhibition of human uPAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VT3PubMed
TargetTissue-type plasminogen activator(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50194743(CHEMBL214814 | diphenyl 1-[(N-alpha-toluenesulfony...)copy SMILEScopy InChI
Affinity DataIC50: 280nMAssay Description:Inhibition of recombinant tPAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VT3PubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50194732(CHEMBL214539 | di-(4-acetamidophenyl) 1-[(N-benzyl...)copy SMILEScopy InChI
Affinity DataIC50: 410nMAssay Description:Inhibition of mouse uPAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VT3PubMed
TargetProthrombin(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50145688(CHEMBL311067 | benzyl (R)-1-((S)-1-(1-(diphenoxyph...)copy SMILEScopy InChI
Affinity DataIC50: 500nMAssay Description:Inhibition of human thrombinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VT3PubMed
TargetProthrombin(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50194743(CHEMBL214814 | diphenyl 1-[(N-alpha-toluenesulfony...)copy SMILEScopy InChI
Affinity DataIC50: 770nMAssay Description:Inhibition of human thrombinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VT3PubMed
TargetPlasminogen(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50194732(CHEMBL214539 | di-(4-acetamidophenyl) 1-[(N-benzyl...)copy SMILEScopy InChI
Affinity DataIC50: 900nMAssay Description:Inhibition of human plasminMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VT3PubMed
TargetPlasminogen(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50194735(CHEMBL215961 | diphenyl 1-[(N-p-cyanobenzenesulfon...)copy SMILEScopy InChI
Affinity DataIC50: 900nMAssay Description:Inhibition of human plasminMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VT3PubMed
TargetPlasminogen(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50194738(CHEMBL386249 | diphenyl 1-[(N-p-bromobenzenesulfon...)copy SMILEScopy InChI
Affinity DataIC50: 900nMAssay Description:Inhibition of human plasminMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VT3PubMed
TargetPlasminogen(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50194744(CHEMBL385897 | diphenyl 1-[(N-naphthalenesulfonyl-...)copy SMILEScopy InChI
Affinity DataIC50: 990nMAssay Description:Inhibition of human plasminMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VT3PubMed
TargetProthrombin(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50194732(CHEMBL214539 | di-(4-acetamidophenyl) 1-[(N-benzyl...)copy SMILEScopy InChI
Affinity DataIC50: 1.50E+3nMAssay Description:Inhibition of human thrombinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VT3PubMed
TargetPlasminogen(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50194745(CHEMBL385900 | diphenyl 1-[(N-2-thiophenesulfonyl-...)copy SMILEScopy InChI
Affinity DataIC50: 1.54E+3nMAssay Description:Inhibition of human plasminMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VT3PubMed
TargetProthrombin(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50194734(CHEMBL386275 | diphenyl 1-[(N-p-methoxybenzenesulf...)copy SMILEScopy InChI
Affinity DataIC50: 1.67E+3nMAssay Description:Inhibition of human thrombinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VT3PubMed
TargetPlasminogen(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50194734(CHEMBL386275 | diphenyl 1-[(N-p-methoxybenzenesulf...)copy SMILEScopy InChI
Affinity DataIC50: 1.70E+3nMAssay Description:Inhibition of human plasminMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VT3PubMed
TargetPlasminogen(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50194741(CHEMBL385158 | diphenyl 1-[(N-benzenesulfonyl-D-se...)copy SMILEScopy InChI
Affinity DataIC50: 1.90E+3nMAssay Description:Inhibition of human plasminMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VT3PubMed
TargetPlasminogen(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50145689(CHEMBL80844 | [1-[(S)-2-((R)-2-Benzyloxycarbonylam...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+3nMAssay Description:Inhibition of human plasminMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VT3PubMed
TargetProthrombin(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50194738(CHEMBL386249 | diphenyl 1-[(N-p-bromobenzenesulfon...)copy SMILEScopy InChI
Affinity DataIC50: 2.98E+3nMAssay Description:Inhibition of human thrombinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VT3PubMed
TargetTissue-type plasminogen activator(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50194741(CHEMBL385158 | diphenyl 1-[(N-benzenesulfonyl-D-se...)copy SMILEScopy InChI
Affinity DataIC50: 3.10E+3nMAssay Description:Inhibition of recombinant tPAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VT3PubMed
TargetTissue-type plasminogen activator(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50194745(CHEMBL385900 | diphenyl 1-[(N-2-thiophenesulfonyl-...)copy SMILEScopy InChI
Affinity DataIC50: 3.40E+3nMAssay Description:Inhibition of recombinant tPAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VT3PubMed
TargetTissue-type plasminogen activator(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50194736(CHEMBL189823 | diphenyl 1-[(N-o,o-dimethylbenzoyl-...)copy SMILEScopy InChI
Affinity DataIC50: 3.60E+3nMAssay Description:Inhibition of recombinant tPAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VT3PubMed
TargetTissue-type plasminogen activator(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50194738(CHEMBL386249 | diphenyl 1-[(N-p-bromobenzenesulfon...)copy SMILEScopy InChI
Affinity DataIC50: 3.70E+3nMAssay Description:Inhibition of recombinant tPAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VT3PubMed
TargetPlasminogen(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50194736(CHEMBL189823 | diphenyl 1-[(N-o,o-dimethylbenzoyl-...)copy SMILEScopy InChI
Affinity DataIC50: 4.20E+3nMAssay Description:Inhibition of human plasminMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VT3PubMed
TargetTissue-type plasminogen activator(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50194734(CHEMBL386275 | diphenyl 1-[(N-p-methoxybenzenesulf...)copy SMILEScopy InChI
Affinity DataIC50: 4.30E+3nMAssay Description:Inhibition of recombinant tPAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VT3PubMed
TargetProthrombin(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50194745(CHEMBL385900 | diphenyl 1-[(N-2-thiophenesulfonyl-...)copy SMILEScopy InChI
Affinity DataIC50: 4.30E+3nMAssay Description:Inhibition of human thrombinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VT3PubMed
TargetTissue-type plasminogen activator(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50194744(CHEMBL385897 | diphenyl 1-[(N-naphthalenesulfonyl-...)copy SMILEScopy InChI
Affinity DataIC50: 4.40E+3nMAssay Description:Inhibition of recombinant tPAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VT3PubMed
TargetTissue-type plasminogen activator(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50145689(CHEMBL80844 | [1-[(S)-2-((R)-2-Benzyloxycarbonylam...)copy SMILEScopy InChI
Affinity DataIC50: 4.60E+3nMAssay Description:Inhibition of recombinant tPAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VT3PubMed
TargetProthrombin(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50194741(CHEMBL385158 | diphenyl 1-[(N-benzenesulfonyl-D-se...)copy SMILEScopy InChI
Affinity DataIC50: 4.90E+3nMAssay Description:Inhibition of human thrombinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VT3PubMed
TargetPlasminogen(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50194740(CHEMBL404226 | diphenyl 1-[(N-p-methylbenzoyl-D-se...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+3nMAssay Description:Inhibition of human plasminMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VT3PubMed
TargetPlasminogen(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50194733(CHEMBL411215 | diphenyl 1-[(N-1-adamantanyl-D-sery...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+3nMAssay Description:Inhibition of human plasminMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VT3PubMed
TargetTissue-type plasminogen activator(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50194746(CHEMBL405546 | diphenyl 1-[(N-o-methylbenzoyl-D-se...)copy SMILEScopy InChI
Affinity DataIC50: 5.50E+3nMAssay Description:Inhibition of recombinant tPAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VT3PubMed
TargetProthrombin(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50194744(CHEMBL385897 | diphenyl 1-[(N-naphthalenesulfonyl-...)copy SMILEScopy InChI
Affinity DataIC50: 6.00E+3nMAssay Description:Inhibition of human thrombinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VT3PubMed
TargetProthrombin(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50194733(CHEMBL411215 | diphenyl 1-[(N-1-adamantanyl-D-sery...)copy SMILEScopy InChI
Affinity DataIC50: 6.00E+3nMAssay Description:Inhibition of human thrombinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VT3PubMed
TargetProthrombin(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50194736(CHEMBL189823 | diphenyl 1-[(N-o,o-dimethylbenzoyl-...)copy SMILEScopy InChI
Affinity DataIC50: 6.30E+3nMAssay Description:Inhibition of human thrombinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VT3PubMed
TargetTissue-type plasminogen activator(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50194732(CHEMBL214539 | di-(4-acetamidophenyl) 1-[(N-benzyl...)copy SMILEScopy InChI
Affinity DataIC50: 6.40E+3nMAssay Description:Inhibition of recombinant tPAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VT3PubMed
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