Target/Host (Institution) | Ligand | Target/Host Links | Ligand Links | Trg + Lig Links | Ki nM | ΔG° kJ/mole | IC50 nM | Kd nM | EC50/IC50 nM | koff s-1 | kon M-1s-1 | pH | Temp °C |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Prothrombin (Homo sapiens (Human)) | BDBM50291004 (4-[2-(1-Carbamimidoyl-2-hydroxy-piperidin-3-ylcarb...) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem | Article | n/a | n/a | 1.10 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA Curated by ChEMBL | Assay Description Compound was evaluated in vitro for the inhibitory concentration required to inhibit human serine protease enzyme thrombin (FIIa) by 50% | Bioorg Med Chem Lett 7: 331-336 (1997) Article DOI: 10.1016/S0960-894X(97)00004-8 BindingDB Entry DOI: 10.7270/Q2Z03850 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Serine protease 1 (Homo sapiens (Human)) | BDBM50291004 (4-[2-(1-Carbamimidoyl-2-hydroxy-piperidin-3-ylcarb...) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem | Article | n/a | n/a | 1.40 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA Curated by ChEMBL | Assay Description Compound was evaluated in vitro for the inhibitory concentration required to inhibit human serine protease enzyme human trypsin by 50% | Bioorg Med Chem Lett 7: 331-336 (1997) Article DOI: 10.1016/S0960-894X(97)00004-8 BindingDB Entry DOI: 10.7270/Q2Z03850 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Serine protease 1 (Homo sapiens (Human)) | BDBM50291006 (4-[2-(1-Carbamimidoyl-2-hydroxy-piperidin-3-ylcarb...) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article | n/a | n/a | 2.60 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA Curated by ChEMBL | Assay Description Compound was evaluated in vitro for the inhibitory concentration required to inhibit human serine protease enzyme human trypsin by 50% | Bioorg Med Chem Lett 7: 331-336 (1997) Article DOI: 10.1016/S0960-894X(97)00004-8 BindingDB Entry DOI: 10.7270/Q2Z03850 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Prothrombin (Homo sapiens (Human)) | BDBM50291006 (4-[2-(1-Carbamimidoyl-2-hydroxy-piperidin-3-ylcarb...) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article | n/a | n/a | 5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA Curated by ChEMBL | Assay Description Compound was evaluated in vitro for the inhibitory concentration required to inhibit human serine protease enzyme thrombin (FIIa) by 50% | Bioorg Med Chem Lett 7: 331-336 (1997) Article DOI: 10.1016/S0960-894X(97)00004-8 BindingDB Entry DOI: 10.7270/Q2Z03850 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Prothrombin (Homo sapiens (Human)) | BDBM50071693 (CHEMBL38927 | CVS-1578 | N-((S)-1-Carbamimidoyl-2-...) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article | n/a | n/a | 6.20 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA Curated by ChEMBL | Assay Description Compound was evaluated in vitro for the inhibitory concentration required to inhibit human serine protease enzyme thrombin (FIIa) by 50% | Bioorg Med Chem Lett 7: 331-336 (1997) Article DOI: 10.1016/S0960-894X(97)00004-8 BindingDB Entry DOI: 10.7270/Q2Z03850 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Serine protease 1 (Homo sapiens (Human)) | BDBM50291005 (5-Oxo-6-phenylmethanesulfonylamino-hexahydro-thiaz...) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article | n/a | n/a | 12 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA Curated by ChEMBL | Assay Description Compound was evaluated in vitro for the inhibitory concentration required to inhibit human serine protease enzyme human trypsin by 50% | Bioorg Med Chem Lett 7: 331-336 (1997) Article DOI: 10.1016/S0960-894X(97)00004-8 BindingDB Entry DOI: 10.7270/Q2Z03850 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Plasminogen (Homo sapiens (Human)) | BDBM50291006 (4-[2-(1-Carbamimidoyl-2-hydroxy-piperidin-3-ylcarb...) | PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article | n/a | n/a | 15 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA Curated by ChEMBL | Assay Description Compound was evaluated in vitro for the inhibitory concentration required to inhibit human serine protease enzyme plasmin by 50% | Bioorg Med Chem Lett 7: 331-336 (1997) Article DOI: 10.1016/S0960-894X(97)00004-8 BindingDB Entry DOI: 10.7270/Q2Z03850 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Prothrombin (Homo sapiens (Human)) | BDBM50291005 (5-Oxo-6-phenylmethanesulfonylamino-hexahydro-thiaz...) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article | n/a | n/a | 16 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA Curated by ChEMBL | Assay Description Compound was evaluated in vitro for the inhibitory concentration required to inhibit human serine protease enzyme thrombin (FIIa) by 50% | Bioorg Med Chem Lett 7: 331-336 (1997) Article DOI: 10.1016/S0960-894X(97)00004-8 BindingDB Entry DOI: 10.7270/Q2Z03850 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Coagulation factor X (Homo sapiens (Human)) | BDBM50291006 (4-[2-(1-Carbamimidoyl-2-hydroxy-piperidin-3-ylcarb...) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article | n/a | n/a | 30 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA Curated by ChEMBL | Assay Description Compound was evaluated in vitro for the inhibitory concentration required to inhibit Coagulation factor X by 50% | Bioorg Med Chem Lett 7: 331-336 (1997) Article DOI: 10.1016/S0960-894X(97)00004-8 BindingDB Entry DOI: 10.7270/Q2Z03850 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Coagulation factor X (Homo sapiens (Human)) | BDBM50291004 (4-[2-(1-Carbamimidoyl-2-hydroxy-piperidin-3-ylcarb...) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem | Article | n/a | n/a | 290 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA Curated by ChEMBL | Assay Description Compound was evaluated in vitro for the inhibitory concentration required to inhibit Coagulation factor X by 50% | Bioorg Med Chem Lett 7: 331-336 (1997) Article DOI: 10.1016/S0960-894X(97)00004-8 BindingDB Entry DOI: 10.7270/Q2Z03850 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Plasminogen (Homo sapiens (Human)) | BDBM50291004 (4-[2-(1-Carbamimidoyl-2-hydroxy-piperidin-3-ylcarb...) | PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem | Article | n/a | n/a | 315 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA Curated by ChEMBL | Assay Description Compound was evaluated in vitro for the inhibitory concentration required to inhibit human serine protease enzyme plasmin by 50% | Bioorg Med Chem Lett 7: 331-336 (1997) Article DOI: 10.1016/S0960-894X(97)00004-8 BindingDB Entry DOI: 10.7270/Q2Z03850 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Serine protease 1 (Homo sapiens (Human)) | BDBM50071693 (CHEMBL38927 | CVS-1578 | N-((S)-1-Carbamimidoyl-2-...) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article | n/a | n/a | 791 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA Curated by ChEMBL | Assay Description Compound was evaluated in vitro for the inhibitory concentration required to inhibit human serine protease enzyme human trypsin by 50% | Bioorg Med Chem Lett 7: 331-336 (1997) Article DOI: 10.1016/S0960-894X(97)00004-8 BindingDB Entry DOI: 10.7270/Q2Z03850 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Plasminogen (Homo sapiens (Human)) | BDBM50291005 (5-Oxo-6-phenylmethanesulfonylamino-hexahydro-thiaz...) | PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article | n/a | n/a | 923 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA Curated by ChEMBL | Assay Description Compound was evaluated in vitro for the inhibitory concentration required to inhibit human serine protease enzyme plasmin by 50% | Bioorg Med Chem Lett 7: 331-336 (1997) Article DOI: 10.1016/S0960-894X(97)00004-8 BindingDB Entry DOI: 10.7270/Q2Z03850 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Coagulation factor X (Homo sapiens (Human)) | BDBM50071693 (CHEMBL38927 | CVS-1578 | N-((S)-1-Carbamimidoyl-2-...) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article | n/a | n/a | >2.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA Curated by ChEMBL | Assay Description Compound was evaluated in vitro for the inhibitory concentration required to inhibit Coagulation factor X by 50% | Bioorg Med Chem Lett 7: 331-336 (1997) Article DOI: 10.1016/S0960-894X(97)00004-8 BindingDB Entry DOI: 10.7270/Q2Z03850 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Coagulation factor X (Homo sapiens (Human)) | BDBM50291005 (5-Oxo-6-phenylmethanesulfonylamino-hexahydro-thiaz...) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article | n/a | n/a | >2.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA Curated by ChEMBL | Assay Description Compound was evaluated in vitro for the inhibitory concentration required to inhibit Coagulation factor X by 50% | Bioorg Med Chem Lett 7: 331-336 (1997) Article DOI: 10.1016/S0960-894X(97)00004-8 BindingDB Entry DOI: 10.7270/Q2Z03850 | |||||||||||
More data for this Ligand-Target Pair |