Compile Data Set for Download or QSAR
Found 115 with Last Name = 'bergum' and Initial = 'pw'
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
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
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
TargetProthrombin(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50073429(CHEMBL82032 | CHEMBL84575 | N-((S)-1-Carbamimidoyl...)copy SMILEScopy InChI
Affinity DataIC50: 0.710nMAssay Description:In vitro inhibitory activity of the compound against human enzyme thrombinMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26M361RPubMed
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
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
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
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
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
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
TargetSerine protease 1(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50081092(CHEMBL85238 | N-((S)-1-Carbamimidoyl-2-hydroxy-pip...)copy SMILEScopy InChI
Affinity DataIC50: 1.5nMAssay Description:In vitro inhibitory activity of the compound against human enzyme trypsinMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26M361RPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50081092(CHEMBL85238 | N-((S)-1-Carbamimidoyl-2-hydroxy-pip...)copy SMILEScopy InChI
Affinity DataIC50: 1.90nMAssay Description:In vitro inhibitory activity of the compound against human enzyme Coagulation factor XMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26M361RPubMed
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
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
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
TargetCoagulation factor X(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50081088(CHEMBL316213 | N-((S)-1-Carbamimidoyl-2-hydroxy-pi...)copy SMILEScopy InChI
Affinity DataIC50: 3.60nMAssay Description:In vitro inhibitory activity against human prothrombinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26M361RPubMed
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
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
TargetCoagulation factor X(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50081087(CHEMBL87947 | N-((S)-1-Carbamimidoyl-2-hydroxy-pip...)copy SMILEScopy InChI
Affinity DataIC50: 7.20nMAssay Description:In vitro inhibitory activity of the compound against human enzyme Coagulation factor XMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26M361RPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50081086(CHEMBL314576 | N-((S)-1-Carbamimidoyl-2-hydroxy-pi...)copy SMILEScopy InChI
Affinity DataIC50: 7.30nMAssay Description:In vitro inhibitory activity of the compound against prothrombinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26M361RPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50081090(CHEMBL87502 | N-((S)-1-Carbamimidoyl-2-hydroxy-pip...)copy SMILEScopy InChI
Affinity DataIC50: 8.60nMAssay Description:In vitro inhibitory activity of the compound against human enzyme Coagulation factor XMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26M361RPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50081092(CHEMBL85238 | N-((S)-1-Carbamimidoyl-2-hydroxy-pip...)copy SMILEScopy InChI
Affinity DataIC50: 9.90nMAssay Description:In vitro inhibitory activity against human prothrombinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26M361RPubMed
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
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
TargetCoagulation factor X(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50081086(CHEMBL314576 | N-((S)-1-Carbamimidoyl-2-hydroxy-pi...)copy SMILEScopy InChI
Affinity DataIC50: 17nMAssay Description:In vitro inhibitory activity against human prothrombinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26M361RPubMed
TargetProthrombin(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50081093(CHEMBL88079 | N-((S)-1-Carbamimidoyl-2-hydroxy-pip...)copy SMILEScopy InChI
Affinity DataIC50: 18nMAssay Description:In vitro inhibitory activity of the compound against human enzyme thrombinMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26M361RPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50081088(CHEMBL316213 | N-((S)-1-Carbamimidoyl-2-hydroxy-pi...)copy SMILEScopy InChI
Affinity DataIC50: 19nMAssay Description:In vitro inhibitory activity against human prothrombinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26M361RPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50073429(CHEMBL82032 | CHEMBL84575 | N-((S)-1-Carbamimidoyl...)copy SMILEScopy InChI
Affinity DataIC50: 21nMAssay Description:In vitro inhibitory activity of the compound against human enzyme Coagulation factor XMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26M361RPubMed
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
LigandPNGBDBM50081086(CHEMBL314576 | N-((S)-1-Carbamimidoyl-2-hydroxy-pi...)copy SMILEScopy InChI
Affinity DataIC50: 26nMAssay Description:In vitro inhibitory activity of the compound against human enzyme trypsinMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26M361RPubMed
TargetSerine protease 1(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50081088(CHEMBL316213 | N-((S)-1-Carbamimidoyl-2-hydroxy-pi...)copy SMILEScopy InChI
Affinity DataIC50: 27nMAssay Description:In vitro evaluation of inhibition of cleavage of the chromogenic substrate by human enzyme trypsinMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26M361RPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50081090(CHEMBL87502 | N-((S)-1-Carbamimidoyl-2-hydroxy-pip...)copy SMILEScopy InChI
Affinity DataIC50: 27nMAssay Description:In vitro inhibitory activity against human prothrombinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26M361RPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50081089(CHEMBL315454 | N-((S)-1-Carbamimidoyl-2-hydroxy-pi...)copy SMILEScopy InChI
Affinity DataIC50: 29nMAssay Description:In vitro inhibitory activity of the compound against human enzyme Coagulation factor XMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26M361RPubMed
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
TargetCoagulation factor X(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50081087(CHEMBL87947 | N-((S)-1-Carbamimidoyl-2-hydroxy-pip...)copy SMILEScopy InChI
Affinity DataIC50: 35nMAssay Description:In vitro inhibitory activity of the compound against human enzyme Coagulation factor XMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26M361RPubMed
TargetSerine protease 1(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50081089(CHEMBL315454 | N-((S)-1-Carbamimidoyl-2-hydroxy-pi...)copy SMILEScopy InChI
Affinity DataIC50: 40nMAssay Description:In vitro evaluation of inhibition of cleavage of the chromogenic substrate by human enzyme trypsinMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26M361RPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50081091(CHEMBL316376 | N-((S)-1-Carbamimidoyl-2-hydroxy-pi...)copy SMILEScopy InChI
Affinity DataIC50: 49nMAssay Description:In vitro inhibitory activity of the compound against human enzyme Coagulation factor XMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26M361RPubMed
TargetCoagulation factor X(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50081089(CHEMBL315454 | N-((S)-1-Carbamimidoyl-2-hydroxy-pi...)copy SMILEScopy InChI
Affinity DataIC50: 64nMAssay Description:In vitro inhibitory activity of the compound against human enzyme Coagulation factor XMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26M361RPubMed
TargetSerine protease 1(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50073429(CHEMBL82032 | CHEMBL84575 | N-((S)-1-Carbamimidoyl...)copy SMILEScopy InChI
Affinity DataIC50: 75nMAssay Description:In vitro inhibitory activity of the compound against human enzyme trypsinMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26M361RPubMed
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
TargetSerine protease 1(Homo sapiens (Human))
Corvas International, Inc.

Curated by ChEMBL
LigandPNGBDBM50081090(CHEMBL87502 | N-((S)-1-Carbamimidoyl-2-hydroxy-pip...)copy SMILEScopy InChI
Affinity DataIC50: 77nMAssay Description:In vitro evaluation of inhibition of cleavage of the chromogenic substrate by human enzyme trypsinMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26M361RPubMed
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