Compile Data Set for Download or QSAR
Report error Found 107 Enz. Inhib. hit(s) with all data for entry = 50011742
TargetSerine protease 1(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110023(2-(3-Hydroxy-2-phenylmethanesulfonylamino-propiony...)
Affinity DataKi:  3.20nMAssay Description:In vitro inhibition of trypsin.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetSerine protease 1(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110025(N-(BENZYLSULFONYL)-D-SERYL-N-{4-[AMINO(IMINO)METHY...)
Affinity DataKi:  3.30nMAssay Description:In vitro inhibition of trypsin.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetSerine protease 1(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110016(Carbonic acid 2-[1-(4-carbamimidoyl-benzylcarbamoy...)
Affinity DataKi:  4.80nMAssay Description:In vitro inhibition of trypsin.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetUrokinase-type plasminogen activator(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110025(N-(BENZYLSULFONYL)-D-SERYL-N-{4-[AMINO(IMINO)METHY...)
Affinity DataKi:  7.70nMAssay Description:In vitro inhibition of plasminogen activator urokinase after a 30 min incubation period.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProthrombin(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110023(2-(3-Hydroxy-2-phenylmethanesulfonylamino-propiony...)
Affinity DataKi:  12nMAssay Description:In vitro inhibition of thrombin.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetUrokinase-type plasminogen activator(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110023(2-(3-Hydroxy-2-phenylmethanesulfonylamino-propiony...)
Affinity DataKi:  13nMAssay Description:In vitro inhibition of plasminogen activator urokinase after a 30 min incubation period.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetUrokinase-type plasminogen activator(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110015(N-(BENZYLSULFONYL)SERYL-N~1~-{4-[AMINO(IMINO)METHY...)
Affinity DataKi:  36nMAssay Description:In vitro inhibition of plasminogen activator urokinase after a 30 min incubation period.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetUrokinase-type plasminogen activator(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110016(Carbonic acid 2-[1-(4-carbamimidoyl-benzylcarbamoy...)
Affinity DataKi:  43nMAssay Description:In vitro inhibition of plasminogen activator urokinase after a 30 min incubation period.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetUrokinase-type plasminogen activator(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110014(N-[(4-Carbamimidoyl-benzylcarbamoyl)-methyl]-2-cyc...)
Affinity DataKi:  48nMAssay Description:In vitro inhibition of plasminogen activator urokinase after a 30 min incubation period.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProthrombin(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110016(Carbonic acid 2-[1-(4-carbamimidoyl-benzylcarbamoy...)
Affinity DataKi:  50nMAssay Description:In vitro inhibition of thrombin.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetSerine protease 1(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110019(Carbonic acid 2-{[(4-carbamimidoyl-benzylcarbamoyl...)
Affinity DataKi:  64nMAssay Description:In vitro inhibition of trypsin.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetSerine protease 1(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110014(N-[(4-Carbamimidoyl-benzylcarbamoyl)-methyl]-2-cyc...)
Affinity DataKi:  110nMAssay Description:In vitro inhibition of trypsin.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProthrombin(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110025(N-(BENZYLSULFONYL)-D-SERYL-N-{4-[AMINO(IMINO)METHY...)
Affinity DataKi:  110nMAssay Description:In vitro inhibition of thrombin.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetSerine protease 1(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110024(Carbonic acid 2-{[(4-carbamimidoyl-benzylcarbamoyl...)
Affinity DataKi:  120nMAssay Description:In vitro inhibition of trypsin.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetPlasminogen(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110023(2-(3-Hydroxy-2-phenylmethanesulfonylamino-propiony...)
Affinity DataKi:  150nMAssay Description:In vitro inhibition of Plasmin.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetPlasminogen(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110016(Carbonic acid 2-[1-(4-carbamimidoyl-benzylcarbamoy...)
Affinity DataKi:  150nMAssay Description:In vitro inhibition of Plasmin.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetSerine protease 1(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110015(N-(BENZYLSULFONYL)SERYL-N~1~-{4-[AMINO(IMINO)METHY...)
Affinity DataKi:  150nMAssay Description:In vitro inhibition of trypsin.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCoagulation factor X(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110019(Carbonic acid 2-{[(4-carbamimidoyl-benzylcarbamoyl...)
Affinity DataKi:  340nMAssay Description:In vitro inhibition of Coagulation factor Xa.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetUrokinase-type plasminogen activator(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110019(Carbonic acid 2-{[(4-carbamimidoyl-benzylcarbamoyl...)
Affinity DataKi:  390nMAssay Description:In vitro inhibition of plasminogen activator urokinase after a 30 min incubation period.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCoagulation factor X(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110016(Carbonic acid 2-[1-(4-carbamimidoyl-benzylcarbamoy...)
Affinity DataKi:  410nMAssay Description:In vitro inhibition of Coagulation factor Xa.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetUrokinase-type plasminogen activator(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110010(N-[(4-Carbamimidoyl-benzylcarbamoyl)-methyl]-3-hyd...)
Affinity DataKi:  490nMAssay Description:In vitro inhibition of plasminogen activator urokinase after a 30 min incubation period.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetUrokinase-type plasminogen activator(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110024(Carbonic acid 2-{[(4-carbamimidoyl-benzylcarbamoyl...)
Affinity DataKi:  500nMAssay Description:In vitro inhibition of plasminogen activator urokinase after a 30 min incubation period.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCoagulation factor X(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110024(Carbonic acid 2-{[(4-carbamimidoyl-benzylcarbamoyl...)
Affinity DataKi:  500nMAssay Description:In vitro inhibition of Coagulation factor Xa.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetPlasminogen(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110025(N-(BENZYLSULFONYL)-D-SERYL-N-{4-[AMINO(IMINO)METHY...)
Affinity DataKi:  540nMAssay Description:In vitro inhibition of Plasmin.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetSerine protease 1(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110012(N-(4-Carbamimidoyl-benzyl)-2-(naphthalene-2-sulfon...)
Affinity DataKi:  650nMAssay Description:In vitro inhibition of trypsin.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetSerine protease 1(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110010(N-[(4-Carbamimidoyl-benzylcarbamoyl)-methyl]-3-hyd...)
Affinity DataKi:  900nMAssay Description:In vitro inhibition of trypsin.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetUrokinase-type plasminogen activator(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110008(N-[(4-Carbamimidoyl-benzylcarbamoyl)-methyl]-3-hyd...)
Affinity DataKi:  1.20E+3nMAssay Description:In vitro inhibition of plasminogen activator urokinase after a 30 min incubation period.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetUrokinase-type plasminogen activator(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110026(N-[(4-Carbamimidoyl-benzylcarbamoyl)-methyl]-3-hyd...)
Affinity DataKi:  1.50E+3nMAssay Description:In vitro inhibition of plasminogen activator urokinase after a 30 min incubation period.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetSerine protease 1(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110006(N-[(4-Carbamimidoyl-benzylcarbamoyl)-methyl]-3-hyd...)
Affinity DataKi:  1.70E+3nMAssay Description:In vitro inhibition of trypsin.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetSerine protease 1(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110008(N-[(4-Carbamimidoyl-benzylcarbamoyl)-methyl]-3-hyd...)
Affinity DataKi:  1.80E+3nMAssay Description:In vitro inhibition of trypsin.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCoagulation factor X(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110014(N-[(4-Carbamimidoyl-benzylcarbamoyl)-methyl]-2-cyc...)
Affinity DataKi:  2.00E+3nMAssay Description:In vitro inhibition of Coagulation factor Xa.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCoagulation factor X(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110023(2-(3-Hydroxy-2-phenylmethanesulfonylamino-propiony...)
Affinity DataKi:  2.00E+3nMAssay Description:In vitro inhibition of Coagulation factor Xa.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCoagulation factor X(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110025(N-(BENZYLSULFONYL)-D-SERYL-N-{4-[AMINO(IMINO)METHY...)
Affinity DataKi:  2.10E+3nMAssay Description:In vitro inhibition of Coagulation factor Xa.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetUrokinase-type plasminogen activator(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110006(N-[(4-Carbamimidoyl-benzylcarbamoyl)-methyl]-3-hyd...)
Affinity DataKi:  2.20E+3nMAssay Description:In vitro inhibition of plasminogen activator urokinase after a 30 min incubation period.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetPlasminogen(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110024(Carbonic acid 2-{[(4-carbamimidoyl-benzylcarbamoyl...)
Affinity DataKi:  2.40E+3nMAssay Description:In vitro inhibition of Plasmin.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetSerine protease 1(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110007(4-tert-Butoxycarbonylamino-4-{[(4-carbamimidoyl-be...)
Affinity DataKi:  2.80E+3nMAssay Description:In vitro inhibition of trypsin.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCoagulation factor X(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110015(N-(BENZYLSULFONYL)SERYL-N~1~-{4-[AMINO(IMINO)METHY...)
Affinity DataKi:  3.00E+3nMAssay Description:In vitro inhibition of Coagulation factor Xa.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProthrombin(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110019(Carbonic acid 2-{[(4-carbamimidoyl-benzylcarbamoyl...)
Affinity DataKi:  3.00E+3nMAssay Description:In vitro inhibition of thrombin.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetUrokinase-type plasminogen activator(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50088982(CHEMBL160253 | CHEMBL367004 | N-[1-(1-Carbamimidoy...)
Affinity DataKi:  3.10E+3nMAssay Description:In vitro inhibition of plasminogen activator urokinase after a 30 min incubation period.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetSerine protease 1(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110013((1-{[(4-Carbamimidoyl-benzylcarbamoyl)-methyl]-car...)
Affinity DataKi:  3.40E+3nMAssay Description:In vitro inhibition of trypsin.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetSerine protease 1(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110026(N-[(4-Carbamimidoyl-benzylcarbamoyl)-methyl]-3-hyd...)
Affinity DataKi:  3.40E+3nMAssay Description:In vitro inhibition of trypsin.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProthrombin(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110024(Carbonic acid 2-{[(4-carbamimidoyl-benzylcarbamoyl...)
Affinity DataKi:  4.00E+3nMAssay Description:In vitro inhibition of thrombin.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetUrokinase-type plasminogen activator(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110005((1-{[(4-Carbamimidoyl-benzylcarbamoyl)-methyl]-car...)
Affinity DataKi:  4.00E+3nMAssay Description:In vitro inhibition of plasminogen activator urokinase after a 30 min incubation period.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetSerine protease 1(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110005((1-{[(4-Carbamimidoyl-benzylcarbamoyl)-methyl]-car...)
Affinity DataKi:  4.30E+3nMAssay Description:In vitro inhibition of trypsin.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetSerine protease 1(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110004((1-{[(4-Carbamimidoyl-benzylcarbamoyl)-methyl]-car...)
Affinity DataKi:  4.50E+3nMAssay Description:In vitro inhibition of trypsin.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetSerine protease 1(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110011(4-Amino-4-{[(4-carbamimidoyl-benzylcarbamoyl)-meth...)
Affinity DataKi:  5.00E+3nMAssay Description:In vitro inhibition of trypsin.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetSerine protease 1(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110018(2-Amino-N-[(4-carbamimidoyl-benzylcarbamoyl)-methy...)
Affinity DataKi:  6.90E+3nMAssay Description:In vitro inhibition of trypsin.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetSerine protease 1(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110017(2-Amino-N-[(4-carbamimidoyl-benzylcarbamoyl)-methy...)
Affinity DataKi:  7.00E+3nMAssay Description:In vitro inhibition of trypsin.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetUrokinase-type plasminogen activator(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110004((1-{[(4-Carbamimidoyl-benzylcarbamoyl)-methyl]-car...)
Affinity DataKi:  9.00E+3nMAssay Description:In vitro inhibition of plasminogen activator urokinase after a 30 min incubation period.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetUrokinase-type plasminogen activator(Human)
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110012(N-(4-Carbamimidoyl-benzyl)-2-(naphthalene-2-sulfon...)
Affinity DataKi:  9.20E+3nMAssay Description:In vitro inhibition of plasminogen activator urokinase after a 30 min incubation period.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
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