Compile Data Set for Download or QSAR
Found 105 with Last Name = 'cohen' and Initial = 'cr'
TargetCoagulation factor X(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50087641(3-{[(R)-1-{[((S)-1-Carbamimidoyl-2-hydroxy-piperid...)copy SMILEScopy InChI
Affinity DataKi:  16nMAssay Description:In vitro inhibition of human trypsin.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M5RPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50087645(4-{2-[(R)-1-{[((S)-1-Carbamimidoyl-2-hydroxy-piper...)copy SMILEScopy InChI
Affinity DataKi:  16nMAssay Description:In vitro inhibitory activity against human Coagulation factor XMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M5RPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50087639((R)-N-[((S)-1-Carbamimidoyl-2-hydroxy-piperidin-3-...)copy SMILEScopy InChI
Affinity DataKi:  23nMAssay Description:Concentration of the compound required for classical fast inhibition of cleavage of the chromogenic substrate by human enzyme Coagulation factor X in...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M5RPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50087647(CHEMBL162277 | [(R)-1-{[((S)-1-Carbamimidoyl-2-hyd...)copy SMILEScopy InChI
Affinity DataKi:  23nMAssay Description:In vitro inhibitory activity against human Coagulation factor XMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M5RPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50087644((R)-N-[((S)-1-Carbamimidoyl-2-hydroxy-piperidin-3-...)copy SMILEScopy InChI
Affinity DataIC50: 0.830nMAssay Description:In vitro inhibition of human Coagulation factor X.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M5RPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50087638((R)-5-Guanidino-2-phenylmethanesulfonylamino-penta...)copy SMILEScopy InChI
Affinity DataIC50: 0.900nMAssay Description:In vitro inhibition of human Coagulation factor X.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M5RPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50087635(((R)-1-{[((S)-1-Carbamimidoyl-2-hydroxy-piperidin-...)copy SMILEScopy InChI
Affinity DataIC50: 0.900nMAssay Description:In vitro inhibition of human Coagulation factor X.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M5RPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50087635(((R)-1-{[((S)-1-Carbamimidoyl-2-hydroxy-piperidin-...)copy SMILEScopy InChI
Affinity DataIC50: 0.900nMAssay Description:Inhibition of human VCAM and Ramos cell VLA-4 interactionMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M5RPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50087635(((R)-1-{[((S)-1-Carbamimidoyl-2-hydroxy-piperidin-...)copy SMILEScopy InChI
Affinity DataIC50: 0.900nMAssay Description:Inhibition of human VCAM and Ramos cell VLA-4 interactionMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M5RPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50087636((R)-N-[((S)-1-Carbamimidoyl-2-hydroxy-piperidin-3-...)copy SMILEScopy InChI
Affinity DataIC50: 0.920nMAssay Description:Inhibition of human VCAM and Ramos cell VLA-4 interactionMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M5RPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50087636((R)-N-[((S)-1-Carbamimidoyl-2-hydroxy-piperidin-3-...)copy SMILEScopy InChI
Affinity DataIC50: 0.920nMAssay Description:In vitro inhibition of human Coagulation factor X.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M5RPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50087643(2-{[(R)-1-{[((S)-1-Carbamimidoyl-2-hydroxy-piperid...)copy SMILEScopy InChI
Affinity DataIC50: 0.940nMAssay Description:In vitro inhibition of human Coagulation factor X.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M5RPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50087642(CHEMBL163251 | N-[((S)-1-Carbamimidoyl-2-hydroxy-p...)copy SMILEScopy InChI
Affinity DataIC50: 1.10nMAssay Description:In vitro inhibition of human Coagulation factor X.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M5RPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50087640(2-{[(R)-1-{[((S)-1-Carbamimidoyl-2-hydroxy-piperid...)copy SMILEScopy InChI
Affinity DataIC50: 1.37nMAssay Description:Inhibition of human VCAM binding to VLA-4 of Ramos cells in ELISAMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M5RPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50087640(2-{[(R)-1-{[((S)-1-Carbamimidoyl-2-hydroxy-piperid...)copy SMILEScopy InChI
Affinity DataIC50: 1.40nMAssay Description:In vitro inhibition of human Coagulation factor X.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M5RPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50087637(2-{[(R)-1-{[((S)-1-Carbamimidoyl-2-hydroxy-piperid...)copy SMILEScopy InChI
Affinity DataIC50: 2.10nMAssay Description:In vitro inhibition of human Coagulation factor X.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M5RPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50087637(2-{[(R)-1-{[((S)-1-Carbamimidoyl-2-hydroxy-piperid...)copy SMILEScopy InChI
Affinity DataIC50: 2.10nMAssay Description:Inhibition of human VCAM binding to VLA-4 of Ramos cells in ELISAMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M5RPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50087634(3-{[(R)-1-{[((S)-1-Carbamimidoyl-2-hydroxy-piperid...)copy SMILEScopy InChI
Affinity DataIC50: 2.20nMAssay Description:In vitro inhibition of human Coagulation factor X.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M5RPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50087639((R)-N-[((S)-1-Carbamimidoyl-2-hydroxy-piperidin-3-...)copy SMILEScopy InChI
Affinity DataIC50: 2.60nMAssay Description:Inhibition of human VCAM binding to VLA-4 of Ramos cells in ELISAMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M5RPubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50088982(CHEMBL160253 | CHEMBL367004 | N-[1-(1-Carbamimidoy...)copy SMILEScopy InChI
Affinity DataIC50: 3.10nMAssay Description:The compound was tested in vitro for its inhibitory activity against human urokinase enzyme, activity expressed as IC50More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2765DKBPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50087641(3-{[(R)-1-{[((S)-1-Carbamimidoyl-2-hydroxy-piperid...)copy SMILEScopy InChI
Affinity DataIC50: 4.30nMAssay Description:In vitro inhibition of human Coagulation factor X.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M5RPubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50088978(CHEMBL176515 | N-[1-(1-Carbamimidoyl-2-hydroxy-pip...)copy SMILEScopy InChI
Affinity DataIC50: 5.10nMAssay Description:The compound was tested in vitro for its inhibitory activity against human urokinase enzyme, activity expressed as IC50More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2765DKBPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50087646(2-{[(R)-1-{[((S)-1-Carbamimidoyl-2-hydroxy-piperid...)copy SMILEScopy InChI
Affinity DataIC50: 5.30nMAssay Description:Concentration of the compound required to inhibit the cleavage of the chromogenic substrate by human enzyme Coagulation factor X in vitroMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M5RPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50087646(2-{[(R)-1-{[((S)-1-Carbamimidoyl-2-hydroxy-piperid...)copy SMILEScopy InChI
Affinity DataIC50: 5.70nMAssay Description:In vitro inhibition of human plasmin.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M5RPubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50088984(2-Benzenesulfonylamino-N-[1-(1-carbamimidoyl-2-hyd...)copy SMILEScopy InChI
Affinity DataIC50: 10nMAssay Description:The compound was tested in vitro for its inhibitory activity against human urokinase enzyme, activity expressed as IC50More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2765DKBPubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50088979(CHEMBL366666 | {(R)-2-[2-((S)-1-Carbamimidoyl-2-hy...)copy SMILEScopy InChI
Affinity DataIC50: 11nMAssay Description:The compound was tested in vitro for its inhibitory activity against human urokinase enzyme, activity expressed as IC50More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2765DKBPubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50088985(CHEMBL369042 | {2-[2-(1-Carbamimidoyl-2-hydroxy-pi...)copy SMILEScopy InChI
Affinity DataIC50: 12nMAssay Description:The compound was tested in vitro for its inhibitory activity against human urokinase enzyme, activity expressed as IC50More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2765DKBPubMed
TargetSerine protease 1(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50087640(2-{[(R)-1-{[((S)-1-Carbamimidoyl-2-hydroxy-piperid...)copy SMILEScopy InChI
Affinity DataIC50: 15nMAssay Description:Inhibition of human VCAM and Ramos cell VLA-4 interactionMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M5RPubMed
TargetSerine protease 1(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50087640(2-{[(R)-1-{[((S)-1-Carbamimidoyl-2-hydroxy-piperid...)copy SMILEScopy InChI
Affinity DataIC50: 15nMAssay Description:In vitro inhibition of human trypsin.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M5RPubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50088977(CHEMBL177557 | {1-[1-(1-Carbamimidoyl-2-hydroxy-pi...)copy SMILEScopy InChI
Affinity DataIC50: 19nMAssay Description:The compound was tested in vitro for its inhibitory activity against human urokinase enzyme, activity expressed as IC50More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2765DKBPubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50088987(CHEMBL174813 | {1-[1-(1-Carbamimidoyl-2-hydroxy-pi...)copy SMILEScopy InChI
Affinity DataIC50: 23nMAssay Description:The compound was tested in vitro for its inhibitory activity against human urokinase enzyme, activity expressed as IC50More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2765DKBPubMed
TargetSerine protease 1(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50087642(CHEMBL163251 | N-[((S)-1-Carbamimidoyl-2-hydroxy-p...)copy SMILEScopy InChI
Affinity DataIC50: 25nMAssay Description:In vitro inhibition of human trypsin.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M5RPubMed
TargetSerine protease 1(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50087636((R)-N-[((S)-1-Carbamimidoyl-2-hydroxy-piperidin-3-...)copy SMILEScopy InChI
Affinity DataIC50: 31nMAssay Description:In vitro inhibition of human trypsin.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M5RPubMed
TargetSerine protease 1(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50087636((R)-N-[((S)-1-Carbamimidoyl-2-hydroxy-piperidin-3-...)copy SMILEScopy InChI
Affinity DataIC50: 31nMAssay Description:In vitro inhibition of human Coagulation factor X.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M5RPubMed
TargetSerine protease 1(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50087638((R)-5-Guanidino-2-phenylmethanesulfonylamino-penta...)copy SMILEScopy InChI
Affinity DataIC50: 75nMAssay Description:In vitro inhibition of human trypsin.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M5RPubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50088986(CHEMBL433809 | {2-[2-(1-Carbamimidoyl-2-hydroxy-pi...)copy SMILEScopy InChI
Affinity DataIC50: 101nMAssay Description:The compound was tested in vitro for its inhibitory activity against human urokinase enzyme, activity expressed as IC50More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2765DKBPubMed
TargetSerine protease 1(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50087635(((R)-1-{[((S)-1-Carbamimidoyl-2-hydroxy-piperidin-...)copy SMILEScopy InChI
Affinity DataIC50: 115nMAssay Description:In vitro inhibition of human trypsin.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M5RPubMed
TargetPlasminogen(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50088985(CHEMBL369042 | {2-[2-(1-Carbamimidoyl-2-hydroxy-pi...)copy SMILEScopy InChI
Affinity DataIC50: 125nMAssay Description:The compound was tested in vitro for its inhibitory activity against human Plasmin enzyme, activity expressed as IC50More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2765DKBPubMed
TargetSerine protease 1(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50087634(3-{[(R)-1-{[((S)-1-Carbamimidoyl-2-hydroxy-piperid...)copy SMILEScopy InChI
Affinity DataIC50: 145nMAssay Description:In vitro inhibition of human trypsin.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M5RPubMed
TargetSerine protease 1(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50087643(2-{[(R)-1-{[((S)-1-Carbamimidoyl-2-hydroxy-piperid...)copy SMILEScopy InChI
Affinity DataIC50: 147nMAssay Description:In vitro inhibition of human trypsin.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M5RPubMed
TargetSerine protease 1(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50087645(4-{2-[(R)-1-{[((S)-1-Carbamimidoyl-2-hydroxy-piper...)copy SMILEScopy InChI
Affinity DataIC50: 158nMAssay Description:In vitro inhibition of human trypsin.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M5RPubMed
TargetSerine protease 1(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50087644((R)-N-[((S)-1-Carbamimidoyl-2-hydroxy-piperidin-3-...)copy SMILEScopy InChI
Affinity DataIC50: 169nMAssay Description:In vitro inhibition of human trypsin.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M5RPubMed
TargetSerine protease 1(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50087641(3-{[(R)-1-{[((S)-1-Carbamimidoyl-2-hydroxy-piperid...)copy SMILEScopy InChI
Affinity DataIC50: 211nMAssay Description:In vitro inhibition of human trypsin.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M5RPubMed
TargetPlasminogen(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50087641(3-{[(R)-1-{[((S)-1-Carbamimidoyl-2-hydroxy-piperid...)copy SMILEScopy InChI
Affinity DataIC50: 231nMAssay Description:In vitro inhibition of human plasmin.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M5RPubMed
TargetSerine protease 1(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50087637(2-{[(R)-1-{[((S)-1-Carbamimidoyl-2-hydroxy-piperid...)copy SMILEScopy InChI
Affinity DataIC50: 240nMAssay Description:Inhibition of human VCAM and Ramos cell VLA-4 interactionMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M5RPubMed
TargetSerine protease 1(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50087637(2-{[(R)-1-{[((S)-1-Carbamimidoyl-2-hydroxy-piperid...)copy SMILEScopy InChI
Affinity DataIC50: 240nMAssay Description:In vitro inhibition of human trypsin.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M5RPubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50088981(CHEMBL425850 | {1-[1-(1-Carbamimidoyl-2-hydroxy-pi...)copy SMILEScopy InChI
Affinity DataIC50: 261nMAssay Description:The compound was tested in vitro for its inhibitory activity against human urokinase enzyme, activity expressed as IC50More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2765DKBPubMed
TargetPlasminogen(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50088978(CHEMBL176515 | N-[1-(1-Carbamimidoyl-2-hydroxy-pip...)copy SMILEScopy InChI
Affinity DataIC50: 275nMAssay Description:The compound was tested in vitro for its inhibitory activity against human Plasmin enzyme, activity expressed as IC50More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2765DKBPubMed
TargetProthrombin(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50087637(2-{[(R)-1-{[((S)-1-Carbamimidoyl-2-hydroxy-piperid...)copy SMILEScopy InChI
Affinity DataIC50: 352nMAssay Description:In vitro inhibition of human thrombin.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2D50M5RPubMed
TargetPlasminogen(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50088982(CHEMBL160253 | CHEMBL367004 | N-[1-(1-Carbamimidoy...)copy SMILEScopy InChI
Affinity DataIC50: 367nMAssay Description:The compound was tested in vitro for its inhibitory activity against human Plasmin enzyme, activity expressed as IC50More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2765DKBPubMed
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