Compile Data Set for Download or QSAR
maximum 50k data
Found 107 Enz. Inhib. hit(s) with all data for entry = 50011742
TargetSerine protease 1(Homo sapiens (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 ArticlePubMed
TargetSerine protease 1(Homo sapiens (Human))
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110025(CHEMBL158405 | N-(BENZYLSULFONYL)-D-SERYL-N-{4-[AM...)
Affinity DataKi:  3.30nMAssay Description:In vitro inhibition of trypsin.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine protease 1(Homo sapiens (Human))
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110016(CHEMBL433510 | Carbonic acid 2-[1-(4-carbamimidoyl...)
Affinity DataKi:  4.80nMAssay Description:In vitro inhibition of trypsin.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110025(CHEMBL158405 | N-(BENZYLSULFONYL)-D-SERYL-N-{4-[AM...)
Affinity DataKi:  7.70nMAssay Description:In vitro inhibition of plasminogen activator urokinase.More data for this Ligand-Target Pair
TargetProthrombin(Homo sapiens (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 ArticlePubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110023(2-(3-Hydroxy-2-phenylmethanesulfonylamino-propiony...)
Affinity DataKi:  13nMAssay Description:In vitro inhibition of plasminogen activator urokinase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110015(CHEMBL158936 | N-(BENZYLSULFONYL)SERYL-N~1~-{4-[AM...)
Affinity DataKi:  36nMAssay Description:In vitro inhibition of plasminogen activator urokinase.More data for this Ligand-Target Pair
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110016(CHEMBL433510 | Carbonic acid 2-[1-(4-carbamimidoyl...)
Affinity DataKi:  43nMAssay Description:In vitro inhibition of plasminogen activator urokinase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110014(CHEMBL158814 | N-[(4-Carbamimidoyl-benzylcarbamoyl...)
Affinity DataKi:  48nMAssay Description:In vitro inhibition of plasminogen activator urokinase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110016(CHEMBL433510 | Carbonic acid 2-[1-(4-carbamimidoyl...)
Affinity DataKi:  50nMAssay Description:In vitro inhibition of thrombin.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine protease 1(Homo sapiens (Human))
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110019(CHEMBL159162 | Carbonic acid 2-{[(4-carbamimidoyl-...)
Affinity DataKi:  64nMAssay Description:In vitro inhibition of trypsin.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110025(CHEMBL158405 | N-(BENZYLSULFONYL)-D-SERYL-N-{4-[AM...)
Affinity DataKi:  110nMAssay Description:In vitro inhibition of thrombin.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine protease 1(Homo sapiens (Human))
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110014(CHEMBL158814 | N-[(4-Carbamimidoyl-benzylcarbamoyl...)
Affinity DataKi:  110nMAssay Description:In vitro inhibition of trypsin.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine protease 1(Homo sapiens (Human))
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110024(CHEMBL345435 | Carbonic acid 2-{[(4-carbamimidoyl-...)
Affinity DataKi:  120nMAssay Description:In vitro inhibition of trypsin.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlasminogen(Homo sapiens (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 ArticlePubMed
TargetSerine protease 1(Homo sapiens (Human))
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110015(CHEMBL158936 | N-(BENZYLSULFONYL)SERYL-N~1~-{4-[AM...)
Affinity DataKi:  150nMAssay Description:In vitro inhibition of trypsin.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlasminogen(Homo sapiens (Human))
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110016(CHEMBL433510 | Carbonic acid 2-[1-(4-carbamimidoyl...)
Affinity DataKi:  150nMAssay Description:In vitro inhibition of Plasmin.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCoagulation factor X(Homo sapiens (Human))
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110019(CHEMBL159162 | Carbonic acid 2-{[(4-carbamimidoyl-...)
Affinity DataKi:  340nMAssay Description:In vitro inhibition of Coagulation factor Xa.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110019(CHEMBL159162 | Carbonic acid 2-{[(4-carbamimidoyl-...)
Affinity DataKi:  390nMAssay Description:In vitro inhibition of plasminogen activator urokinase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCoagulation factor X(Homo sapiens (Human))
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110016(CHEMBL433510 | Carbonic acid 2-[1-(4-carbamimidoyl...)
Affinity DataKi:  410nMAssay Description:In vitro inhibition of Coagulation factor Xa.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110010(CHEMBL415741 | N-[(4-Carbamimidoyl-benzylcarbamoyl...)
Affinity DataKi:  490nMAssay Description:In vitro inhibition of plasminogen activator urokinase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCoagulation factor X(Homo sapiens (Human))
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110024(CHEMBL345435 | Carbonic acid 2-{[(4-carbamimidoyl-...)
Affinity DataKi:  500nMAssay Description:In vitro inhibition of Coagulation factor Xa.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110024(CHEMBL345435 | Carbonic acid 2-{[(4-carbamimidoyl-...)
Affinity DataKi:  500nMAssay Description:In vitro inhibition of plasminogen activator urokinase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlasminogen(Homo sapiens (Human))
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110025(CHEMBL158405 | N-(BENZYLSULFONYL)-D-SERYL-N-{4-[AM...)
Affinity DataKi:  540nMAssay Description:In vitro inhibition of Plasmin.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine protease 1(Homo sapiens (Human))
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110012(CHEMBL156858 | N-(4-Carbamimidoyl-benzyl)-2-(napht...)
Affinity DataKi:  650nMAssay Description:In vitro inhibition of trypsin.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine protease 1(Homo sapiens (Human))
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110010(CHEMBL415741 | N-[(4-Carbamimidoyl-benzylcarbamoyl...)
Affinity DataKi:  900nMAssay Description:In vitro inhibition of trypsin.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110008(CHEMBL346117 | N-[(4-Carbamimidoyl-benzylcarbamoyl...)
Affinity DataKi:  1.20E+3nMAssay Description:In vitro inhibition of plasminogen activator urokinase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110026(CHEMBL157131 | N-[(4-Carbamimidoyl-benzylcarbamoyl...)
Affinity DataKi:  1.50E+3nMAssay Description:In vitro inhibition of plasminogen activator urokinase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine protease 1(Homo sapiens (Human))
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110006(CHEMBL352009 | N-[(4-Carbamimidoyl-benzylcarbamoyl...)
Affinity DataKi:  1.70E+3nMAssay Description:In vitro inhibition of trypsin.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine protease 1(Homo sapiens (Human))
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110008(CHEMBL346117 | N-[(4-Carbamimidoyl-benzylcarbamoyl...)
Affinity DataKi:  1.80E+3nMAssay Description:In vitro inhibition of trypsin.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCoagulation factor X(Homo sapiens (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 ArticlePubMed
TargetCoagulation factor X(Homo sapiens (Human))
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110014(CHEMBL158814 | N-[(4-Carbamimidoyl-benzylcarbamoyl...)
Affinity DataKi:  2.00E+3nMAssay Description:In vitro inhibition of Coagulation factor Xa.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCoagulation factor X(Homo sapiens (Human))
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110025(CHEMBL158405 | N-(BENZYLSULFONYL)-D-SERYL-N-{4-[AM...)
Affinity DataKi:  2.10E+3nMAssay Description:In vitro inhibition of Coagulation factor Xa.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110006(CHEMBL352009 | N-[(4-Carbamimidoyl-benzylcarbamoyl...)
Affinity DataKi:  2.20E+3nMAssay Description:In vitro inhibition of plasminogen activator urokinase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlasminogen(Homo sapiens (Human))
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110024(CHEMBL345435 | Carbonic acid 2-{[(4-carbamimidoyl-...)
Affinity DataKi:  2.40E+3nMAssay Description:In vitro inhibition of Plasmin.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine protease 1(Homo sapiens (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 ArticlePubMed
TargetCoagulation factor X(Homo sapiens (Human))
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110015(CHEMBL158936 | N-(BENZYLSULFONYL)SERYL-N~1~-{4-[AM...)
Affinity DataKi:  3.00E+3nMAssay Description:In vitro inhibition of Coagulation factor Xa.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110019(CHEMBL159162 | Carbonic acid 2-{[(4-carbamimidoyl-...)
Affinity DataKi:  3.00E+3nMAssay Description:In vitro inhibition of thrombin.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (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 ArticlePubMed
TargetSerine protease 1(Homo sapiens (Human))
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110026(CHEMBL157131 | N-[(4-Carbamimidoyl-benzylcarbamoyl...)
Affinity DataKi:  3.40E+3nMAssay Description:In vitro inhibition of trypsin.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine protease 1(Homo sapiens (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 ArticlePubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (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.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110024(CHEMBL345435 | Carbonic acid 2-{[(4-carbamimidoyl-...)
Affinity DataKi:  4.00E+3nMAssay Description:In vitro inhibition of thrombin.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine protease 1(Homo sapiens (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 ArticlePubMed
TargetSerine protease 1(Homo sapiens (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 ArticlePubMed
TargetSerine protease 1(Homo sapiens (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 ArticlePubMed
TargetSerine protease 1(Homo sapiens (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 ArticlePubMed
TargetSerine protease 1(Homo sapiens (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 ArticlePubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (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.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110012(CHEMBL156858 | N-(4-Carbamimidoyl-benzyl)-2-(napht...)
Affinity DataKi:  9.20E+3nMAssay Description:In vitro inhibition of plasminogen activator urokinase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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