Found 73 hits of Enzyme Inhibition Constant Data 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 |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50083743
(1N-[1-amino(imino)methyl-6-hydroxy-(5S)-tetrahydro...)Show SMILES NC(=N)NCCCC(NS(=O)(=O)Cc1ccccc1)C(=O)NCC(=O)N[C@H]1CCCN(C1O)C(N)=N Show InChI InChI=1S/C21H35N9O5S/c22-20(23)26-10-4-8-15(29-36(34,35)13-14-6-2-1-3-7-14)18(32)27-12-17(31)28-16-9-5-11-30(19(16)33)21(24)25/h1-3,6-7,15-16,19,29,33H,4-5,8-13H2,(H3,24,25)(H,27,32)(H,28,31)(H4,22,23,26)/t15?,16-,19?/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 0.700 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human Factor Xa. |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Serine protease 1
(Homo sapiens (Human)) | BDBM50083747
(CHEMBL325869 | Cinnoline-4-carboxylic acid ((R)-3-...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2cnnc3ccccc23)NS(=O)(=O)Cc2ccccc2)C1O Show InChI InChI=1S/C28H35N9O6S/c29-28(30)37-14-6-11-23(27(37)41)34-24(38)16-32-26(40)22(36-44(42,43)17-18-7-2-1-3-8-18)12-13-31-25(39)20-15-33-35-21-10-5-4-9-19(20)21/h1-5,7-10,15,22-23,27,36,41H,6,11-14,16-17H2,(H3,29,30)(H,31,39)(H,32,40)(H,34,38)/t22-,23+,27?/m1/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 4.20 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human trypsin. |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50083756
(CHEMBL117092 | Isoquinoline-1-carboxylic acid ((R)...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2nccc3ccccc23)NS(=O)(=O)Cc2ccccc2)C1O Show InChI InChI=1S/C29H36N8O6S/c30-29(31)37-16-6-11-23(28(37)41)35-24(38)17-34-26(39)22(36-44(42,43)18-19-7-2-1-3-8-19)13-15-33-27(40)25-21-10-5-4-9-20(21)12-14-32-25/h1-5,7-10,12,14,22-23,28,36,41H,6,11,13,15-18H2,(H3,30,31)(H,33,40)(H,34,39)(H,35,38)/t22-,23+,28?/m1/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 4.90 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human Factor Xa. |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50083754
(CHEMBL420688 | Pyrazine-2-carboxylic acid ((R)-3-{...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2cnccn2)NS(=O)(=O)Cc2ccccc2)C1O Show InChI InChI=1S/C24H33N9O6S/c25-24(26)33-12-4-7-18(23(33)37)31-20(34)14-30-21(35)17(8-9-29-22(36)19-13-27-10-11-28-19)32-40(38,39)15-16-5-2-1-3-6-16/h1-3,5-6,10-11,13,17-18,23,32,37H,4,7-9,12,14-15H2,(H3,25,26)(H,29,36)(H,30,35)(H,31,34)/t17-,18+,23?/m1/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 5 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human Factor Xa. |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50083747
(CHEMBL325869 | Cinnoline-4-carboxylic acid ((R)-3-...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2cnnc3ccccc23)NS(=O)(=O)Cc2ccccc2)C1O Show InChI InChI=1S/C28H35N9O6S/c29-28(30)37-14-6-11-23(27(37)41)34-24(38)16-32-26(40)22(36-44(42,43)17-18-7-2-1-3-8-18)12-13-31-25(39)20-15-33-35-21-10-5-4-9-19(20)21/h1-5,7-10,15,22-23,27,36,41H,6,11-14,16-17H2,(H3,29,30)(H,31,39)(H,32,40)(H,34,38)/t22-,23+,27?/m1/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 5.60 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human Factor Xa. |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50083744
(CHEMBL331807 | N-((R)-3-{[((S)-1-Carbamimidoyl-2-h...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2ccc(=O)[nH]c2)NS(=O)(=O)Cc2ccccc2)C1O Show InChI InChI=1S/C25H34N8O7S/c26-25(27)33-12-4-7-19(24(33)38)31-21(35)14-30-23(37)18(32-41(39,40)15-16-5-2-1-3-6-16)10-11-28-22(36)17-8-9-20(34)29-13-17/h1-3,5-6,8-9,13,18-19,24,32,38H,4,7,10-12,14-15H2,(H3,26,27)(H,28,36)(H,29,34)(H,30,37)(H,31,35)/t18-,19+,24?/m1/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 6.10 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human Factor Xa. |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50083745
(5-Bromo-N-((R)-3-{[((S)-1-carbamimidoyl-2-hydroxy-...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2cncc(Br)c2)NS(=O)(=O)Cc2ccccc2)C1O Show InChI InChI=1S/C25H33BrN8O6S/c26-18-11-17(12-29-13-18)22(36)30-9-8-19(33-41(39,40)15-16-5-2-1-3-6-16)23(37)31-14-21(35)32-20-7-4-10-34(24(20)38)25(27)28/h1-3,5-6,11-13,19-20,24,33,38H,4,7-10,14-15H2,(H3,27,28)(H,30,36)(H,31,37)(H,32,35)/t19-,20+,24?/m1/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 11 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human Factor Xa. |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50083750
(CHEMBL115902 | Quinoline-3-carboxylic acid ((R)-3-...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2cnc3ccccc3c2)NS(=O)(=O)Cc2ccccc2)C1O Show InChI InChI=1S/C29H36N8O6S/c30-29(31)37-14-6-11-24(28(37)41)35-25(38)17-34-27(40)23(36-44(42,43)18-19-7-2-1-3-8-19)12-13-32-26(39)21-15-20-9-4-5-10-22(20)33-16-21/h1-5,7-10,15-16,23-24,28,36,41H,6,11-14,17-18H2,(H3,30,31)(H,32,39)(H,34,40)(H,35,38)/t23-,24+,28?/m1/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 11 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human Factor Xa. |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50083751
(CHEMBL420322 | Pyrazine-2-carboxylic acid ((R)-4-{...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCCNC(=O)c2cnccn2)NS(=O)(=O)Cc2ccccc2)C1O Show InChI InChI=1S/C25H35N9O6S/c26-25(27)34-13-5-9-19(24(34)38)32-21(35)15-31-22(36)18(33-41(39,40)16-17-6-2-1-3-7-17)8-4-10-30-23(37)20-14-28-11-12-29-20/h1-3,6-7,11-12,14,18-19,24,33,38H,4-5,8-10,13,15-16H2,(H3,26,27)(H,30,37)(H,31,36)(H,32,35)/t18-,19+,24?/m1/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 15 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human Factor Xa. |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Serine protease 1
(Homo sapiens (Human)) | BDBM50083742
(CHEMBL324485 | {(R)-1-{[((S)-1-Carbamimidoyl-2-hyd...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2cnc3ccccc3c2)NC(=O)OCc2ccccc2)C1O Show InChI InChI=1S/C30H36N8O6/c31-29(32)38-14-6-11-24(28(38)42)36-25(39)17-35-27(41)23(37-30(43)44-18-19-7-2-1-3-8-19)12-13-33-26(40)21-15-20-9-4-5-10-22(20)34-16-21/h1-5,7-10,15-16,23-24,28,42H,6,11-14,17-18H2,(H3,31,32)(H,33,40)(H,35,41)(H,36,39)(H,37,43)/t23-,24+,28?/m1/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 20 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human trypsin. |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50083749
(CHEMBL323642 | Pyridine-2-carboxylic acid ((R)-3-{...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2ccccn2)NS(=O)(=O)Cc2ccccc2)C1O Show InChI InChI=1S/C25H34N8O6S/c26-25(27)33-14-6-10-20(24(33)37)31-21(34)15-30-23(36)19(11-13-29-22(35)18-9-4-5-12-28-18)32-40(38,39)16-17-7-2-1-3-8-17/h1-5,7-9,12,19-20,24,32,37H,6,10-11,13-16H2,(H3,26,27)(H,29,35)(H,30,36)(H,31,34)/t19-,20+,24?/m1/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 21 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human Factor Xa. |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Serine protease 1
(Homo sapiens (Human)) | BDBM50083744
(CHEMBL331807 | N-((R)-3-{[((S)-1-Carbamimidoyl-2-h...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2ccc(=O)[nH]c2)NS(=O)(=O)Cc2ccccc2)C1O Show InChI InChI=1S/C25H34N8O7S/c26-25(27)33-12-4-7-19(24(33)38)31-21(35)14-30-23(37)18(32-41(39,40)15-16-5-2-1-3-6-16)10-11-28-22(36)17-8-9-20(34)29-13-17/h1-3,5-6,8-9,13,18-19,24,32,38H,4,7,10-12,14-15H2,(H3,26,27)(H,28,36)(H,29,34)(H,30,37)(H,31,35)/t18-,19+,24?/m1/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 27 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human trypsin. |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Serine protease 1
(Homo sapiens (Human)) | BDBM50083753
(CHEMBL116245 | {(R)-1-{[((S)-1-Carbamimidoyl-2-hyd...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2cnccn2)NC(=O)OCc2ccccc2)C1O Show InChI InChI=1S/C25H33N9O6/c26-24(27)34-12-4-7-18(23(34)38)32-20(35)14-31-21(36)17(8-9-30-22(37)19-13-28-10-11-29-19)33-25(39)40-15-16-5-2-1-3-6-16/h1-3,5-6,10-11,13,17-18,23,38H,4,7-9,12,14-15H2,(H3,26,27)(H,30,37)(H,31,36)(H,32,35)(H,33,39)/t17-,18+,23?/m1/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 30 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human trypsin. |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Serine protease 1
(Homo sapiens (Human)) | BDBM50083740
(((R)-3-[(5-Bromo-pyridine-3-carbonyl)-amino]-1-{[(...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2cncc(Br)c2)NC(=O)OCc2ccccc2)C1O Show InChI InChI=1S/C26H33BrN8O6/c27-18-11-17(12-30-13-18)22(37)31-9-8-19(34-26(40)41-15-16-5-2-1-3-6-16)23(38)32-14-21(36)33-20-7-4-10-35(24(20)39)25(28)29/h1-3,5-6,11-13,19-20,24,39H,4,7-10,14-15H2,(H3,28,29)(H,31,37)(H,32,38)(H,33,36)(H,34,40)/t19-,20+,24?/m1/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | >31 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human trypsin. |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Serine protease 1
(Homo sapiens (Human)) | BDBM50083739
(CHEMBL115707 | {(R)-1-{[((S)-1-Carbamimidoyl-2-hyd...)Show SMILES Cc1cnc(cn1)C(=O)NCC[C@@H](NC(=O)OCc1ccccc1)C(=O)NCC(=O)N[C@H]1CCCN(C1O)C(N)=N Show InChI InChI=1S/C26H35N9O6/c1-16-12-31-20(13-30-16)23(38)29-10-9-18(34-26(40)41-15-17-6-3-2-4-7-17)22(37)32-14-21(36)33-19-8-5-11-35(24(19)39)25(27)28/h2-4,6-7,12-13,18-19,24,39H,5,8-11,14-15H2,1H3,(H3,27,28)(H,29,38)(H,32,37)(H,33,36)(H,34,40)/t18-,19+,24?/m1/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 40 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human trypsin. |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50083746
(CHEMBL117716 | Quinoline-2-carboxylic acid ((R)-3-...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2ccc3ccccc3n2)NS(=O)(=O)Cc2ccccc2)C1O Show InChI InChI=1S/C29H36N8O6S/c30-29(31)37-16-6-11-24(28(37)41)35-25(38)17-33-27(40)23(36-44(42,43)18-19-7-2-1-3-8-19)14-15-32-26(39)22-13-12-20-9-4-5-10-21(20)34-22/h1-5,7-10,12-13,23-24,28,36,41H,6,11,14-18H2,(H3,30,31)(H,32,39)(H,33,40)(H,35,38)/t23-,24+,28?/m1/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 44 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human Factor Xa. |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Serine protease 1
(Homo sapiens (Human)) | BDBM50083746
(CHEMBL117716 | Quinoline-2-carboxylic acid ((R)-3-...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2ccc3ccccc3n2)NS(=O)(=O)Cc2ccccc2)C1O Show InChI InChI=1S/C29H36N8O6S/c30-29(31)37-16-6-11-24(28(37)41)35-25(38)17-33-27(40)23(36-44(42,43)18-19-7-2-1-3-8-19)14-15-32-26(39)22-13-12-20-9-4-5-10-21(20)34-22/h1-5,7-10,12-13,23-24,28,36,41H,6,11,14-18H2,(H3,30,31)(H,32,39)(H,33,40)(H,35,38)/t23-,24+,28?/m1/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 59 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human trypsin. |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Serine protease 1
(Homo sapiens (Human)) | BDBM50083743
(1N-[1-amino(imino)methyl-6-hydroxy-(5S)-tetrahydro...)Show SMILES NC(=N)NCCCC(NS(=O)(=O)Cc1ccccc1)C(=O)NCC(=O)N[C@H]1CCCN(C1O)C(N)=N Show InChI InChI=1S/C21H35N9O5S/c22-20(23)26-10-4-8-15(29-36(34,35)13-14-6-2-1-3-7-14)18(32)27-12-17(31)28-16-9-5-11-30(19(16)33)21(24)25/h1-3,6-7,15-16,19,29,33H,4-5,8-13H2,(H3,24,25)(H,27,32)(H,28,31)(H4,22,23,26)/t15?,16-,19?/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 75 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human trypsin. |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Serine protease 1
(Homo sapiens (Human)) | BDBM50083741
(CHEMBL419222 | {(R)-1-{[((S)-1-Carbamimidoyl-2-hyd...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2cn[nH]c2)NC(=O)OCc2ccccc2)C1O Show InChI InChI=1S/C24H33N9O6/c25-23(26)33-10-4-7-18(22(33)37)31-19(34)13-28-21(36)17(8-9-27-20(35)16-11-29-30-12-16)32-24(38)39-14-15-5-2-1-3-6-15/h1-3,5-6,11-12,17-18,22,37H,4,7-10,13-14H2,(H3,25,26)(H,27,35)(H,28,36)(H,29,30)(H,31,34)(H,32,38)/t17-,18+,22?/m1/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| PubMed
| n/a | n/a | 75 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human trypsin. |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50083752
(CHEMBL117678 | N-((R)-3-{[((S)-1-Carbamimidoyl-2-h...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2cccnc2)NS(=O)(=O)Cc2ccccc2)C1O Show InChI InChI=1S/C25H34N8O6S/c26-25(27)33-13-5-9-20(24(33)37)31-21(34)15-30-23(36)19(10-12-29-22(35)18-8-4-11-28-14-18)32-40(38,39)16-17-6-2-1-3-7-17/h1-4,6-8,11,14,19-20,24,32,37H,5,9-10,12-13,15-16H2,(H3,26,27)(H,29,35)(H,30,36)(H,31,34)/t19-,20+,24?/m1/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 79 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human Factor Xa. |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Serine protease 1
(Homo sapiens (Human)) | BDBM50083756
(CHEMBL117092 | Isoquinoline-1-carboxylic acid ((R)...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2nccc3ccccc23)NS(=O)(=O)Cc2ccccc2)C1O Show InChI InChI=1S/C29H36N8O6S/c30-29(31)37-16-6-11-23(28(37)41)35-24(38)17-34-26(39)22(36-44(42,43)18-19-7-2-1-3-8-19)13-15-33-27(40)25-21-10-5-4-9-20(21)12-14-32-25/h1-5,7-10,12,14,22-23,28,36,41H,6,11,13,15-18H2,(H3,30,31)(H,33,40)(H,34,39)(H,35,38)/t22-,23+,28?/m1/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 98 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human trypsin. |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50083753
(CHEMBL116245 | {(R)-1-{[((S)-1-Carbamimidoyl-2-hyd...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2cnccn2)NC(=O)OCc2ccccc2)C1O Show InChI InChI=1S/C25H33N9O6/c26-24(27)34-12-4-7-18(23(34)38)32-20(35)14-31-21(36)17(8-9-30-22(37)19-13-28-10-11-29-19)33-25(39)40-15-16-5-2-1-3-6-16/h1-3,5-6,10-11,13,17-18,23,38H,4,7-9,12,14-15H2,(H3,26,27)(H,30,37)(H,31,36)(H,32,35)(H,33,39)/t17-,18+,23?/m1/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 106 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human Factor Xa. |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50083739
(CHEMBL115707 | {(R)-1-{[((S)-1-Carbamimidoyl-2-hyd...)Show SMILES Cc1cnc(cn1)C(=O)NCC[C@@H](NC(=O)OCc1ccccc1)C(=O)NCC(=O)N[C@H]1CCCN(C1O)C(N)=N Show InChI InChI=1S/C26H35N9O6/c1-16-12-31-20(13-30-16)23(38)29-10-9-18(34-26(40)41-15-17-6-3-2-4-7-17)22(37)32-14-21(36)33-19-8-5-11-35(24(19)39)25(27)28/h2-4,6-7,12-13,18-19,24,39H,5,8-11,14-15H2,1H3,(H3,27,28)(H,29,38)(H,32,37)(H,33,36)(H,34,40)/t18-,19+,24?/m1/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 106 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human Factor Xa. |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Serine protease 1
(Homo sapiens (Human)) | BDBM50083750
(CHEMBL115902 | Quinoline-3-carboxylic acid ((R)-3-...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2cnc3ccccc3c2)NS(=O)(=O)Cc2ccccc2)C1O Show InChI InChI=1S/C29H36N8O6S/c30-29(31)37-14-6-11-24(28(37)41)35-25(38)17-34-27(40)23(36-44(42,43)18-19-7-2-1-3-8-19)12-13-32-26(39)21-15-20-9-4-5-10-22(20)33-16-21/h1-5,7-10,15-16,23-24,28,36,41H,6,11-14,17-18H2,(H3,30,31)(H,32,39)(H,34,40)(H,35,38)/t23-,24+,28?/m1/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 111 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human trypsin. |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Serine protease 1
(Homo sapiens (Human)) | BDBM50083748
(CHEMBL117721 | Pyrazine-2-carboxylic acid ((R)-2-{...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CNC(=O)c2cnccn2)NS(=O)(=O)Cc2ccccc2)C1O Show InChI InChI=1S/C23H31N9O6S/c24-23(25)32-10-4-7-16(22(32)36)30-19(33)13-29-21(35)18(12-28-20(34)17-11-26-8-9-27-17)31-39(37,38)14-15-5-2-1-3-6-15/h1-3,5-6,8-9,11,16,18,22,31,36H,4,7,10,12-14H2,(H3,24,25)(H,28,34)(H,29,35)(H,30,33)/t16-,18+,22?/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 152 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human trypsin. |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Serine protease 1
(Homo sapiens (Human)) | BDBM50083745
(5-Bromo-N-((R)-3-{[((S)-1-carbamimidoyl-2-hydroxy-...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2cncc(Br)c2)NS(=O)(=O)Cc2ccccc2)C1O Show InChI InChI=1S/C25H33BrN8O6S/c26-18-11-17(12-29-13-18)22(36)30-9-8-19(33-41(39,40)15-16-5-2-1-3-6-16)23(37)31-14-21(35)32-20-7-4-10-34(24(20)38)25(27)28/h1-3,5-6,11-13,19-20,24,33,38H,4,7-10,14-15H2,(H3,27,28)(H,30,36)(H,31,37)(H,32,35)/t19-,20+,24?/m1/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 160 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human trypsin. |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Serine protease 1
(Homo sapiens (Human)) | BDBM50083754
(CHEMBL420688 | Pyrazine-2-carboxylic acid ((R)-3-{...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2cnccn2)NS(=O)(=O)Cc2ccccc2)C1O Show InChI InChI=1S/C24H33N9O6S/c25-24(26)33-12-4-7-18(23(33)37)31-20(34)14-30-21(35)17(8-9-29-22(36)19-13-27-10-11-28-19)32-40(38,39)15-16-5-2-1-3-6-16/h1-3,5-6,10-11,13,17-18,23,32,37H,4,7-9,12,14-15H2,(H3,25,26)(H,29,36)(H,30,35)(H,31,34)/t17-,18+,23?/m1/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 166 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human trypsin. |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50083742
(CHEMBL324485 | {(R)-1-{[((S)-1-Carbamimidoyl-2-hyd...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2cnc3ccccc3c2)NC(=O)OCc2ccccc2)C1O Show InChI InChI=1S/C30H36N8O6/c31-29(32)38-14-6-11-24(28(38)42)36-25(39)17-35-27(41)23(37-30(43)44-18-19-7-2-1-3-8-19)12-13-33-26(40)21-15-20-9-4-5-10-22(20)34-16-21/h1-5,7-10,15-16,23-24,28,42H,6,11-14,17-18H2,(H3,31,32)(H,33,40)(H,35,41)(H,36,39)(H,37,43)/t23-,24+,28?/m1/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 169 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human Factor Xa. |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Serine protease 1
(Homo sapiens (Human)) | BDBM50083749
(CHEMBL323642 | Pyridine-2-carboxylic acid ((R)-3-{...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2ccccn2)NS(=O)(=O)Cc2ccccc2)C1O Show InChI InChI=1S/C25H34N8O6S/c26-25(27)33-14-6-10-20(24(33)37)31-21(34)15-30-23(36)19(11-13-29-22(35)18-9-4-5-12-28-18)32-40(38,39)16-17-7-2-1-3-8-17/h1-5,7-9,12,19-20,24,32,37H,6,10-11,13-16H2,(H3,26,27)(H,29,35)(H,30,36)(H,31,34)/t19-,20+,24?/m1/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 223 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human trypsin. |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Plasminogen
(Homo sapiens (Human)) | BDBM50083750
(CHEMBL115902 | Quinoline-3-carboxylic acid ((R)-3-...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2cnc3ccccc3c2)NS(=O)(=O)Cc2ccccc2)C1O Show InChI InChI=1S/C29H36N8O6S/c30-29(31)37-14-6-11-24(28(37)41)35-25(38)17-34-27(40)23(36-44(42,43)18-19-7-2-1-3-8-19)12-13-32-26(39)21-15-20-9-4-5-10-22(20)33-16-21/h1-5,7-10,15-16,23-24,28,36,41H,6,11-14,17-18H2,(H3,30,31)(H,32,39)(H,34,40)(H,35,38)/t23-,24+,28?/m1/s1 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 250 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human thrombolytic protease Plasmin. |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50083748
(CHEMBL117721 | Pyrazine-2-carboxylic acid ((R)-2-{...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CNC(=O)c2cnccn2)NS(=O)(=O)Cc2ccccc2)C1O Show InChI InChI=1S/C23H31N9O6S/c24-23(25)32-10-4-7-16(22(32)36)30-19(33)13-29-21(35)18(12-28-20(34)17-11-26-8-9-27-17)31-39(37,38)14-15-5-2-1-3-6-15/h1-3,5-6,8-9,11,16,18,22,31,36H,4,7,10,12-14H2,(H3,24,25)(H,28,34)(H,29,35)(H,30,33)/t16-,18+,22?/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 311 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human Factor Xa. |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50083738
(CHEMBL115378 | {(R)-1-{[((S)-1-Carbamimidoyl-2-hyd...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2nccc3ccccc23)NC(=O)OCc2ccccc2)C1O Show InChI InChI=1S/C30H36N8O6/c31-29(32)38-16-6-11-23(28(38)42)36-24(39)17-35-26(40)22(37-30(43)44-18-19-7-2-1-3-8-19)13-15-34-27(41)25-21-10-5-4-9-20(21)12-14-33-25/h1-5,7-10,12,14,22-23,28,42H,6,11,13,15-18H2,(H3,31,32)(H,34,41)(H,35,40)(H,36,39)(H,37,43)/t22-,23+,28?/m1/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| PubMed
| n/a | n/a | 313 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human Factor Xa. |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50083740
(((R)-3-[(5-Bromo-pyridine-3-carbonyl)-amino]-1-{[(...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2cncc(Br)c2)NC(=O)OCc2ccccc2)C1O Show InChI InChI=1S/C26H33BrN8O6/c27-18-11-17(12-30-13-18)22(37)31-9-8-19(34-26(40)41-15-16-5-2-1-3-6-16)23(38)32-14-21(36)33-20-7-4-10-35(24(20)39)25(28)29/h1-3,5-6,11-13,19-20,24,39H,4,7-10,14-15H2,(H3,28,29)(H,31,37)(H,32,38)(H,33,36)(H,34,40)/t19-,20+,24?/m1/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 313 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human Factor Xa. |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Serine protease 1
(Homo sapiens (Human)) | BDBM50083751
(CHEMBL420322 | Pyrazine-2-carboxylic acid ((R)-4-{...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCCNC(=O)c2cnccn2)NS(=O)(=O)Cc2ccccc2)C1O Show InChI InChI=1S/C25H35N9O6S/c26-25(27)34-13-5-9-19(24(34)38)32-21(35)15-31-22(36)18(33-41(39,40)16-17-6-2-1-3-7-17)8-4-10-30-23(37)20-14-28-11-12-29-20/h1-3,6-7,11-12,14,18-19,24,33,38H,4-5,8-10,13,15-16H2,(H3,26,27)(H,30,37)(H,31,36)(H,32,35)/t18-,19+,24?/m1/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 324 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human trypsin. |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50083741
(CHEMBL419222 | {(R)-1-{[((S)-1-Carbamimidoyl-2-hyd...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2cn[nH]c2)NC(=O)OCc2ccccc2)C1O Show InChI InChI=1S/C24H33N9O6/c25-23(26)33-10-4-7-18(22(33)37)31-19(34)13-28-21(36)17(8-9-27-20(35)16-11-29-30-12-16)32-24(38)39-14-15-5-2-1-3-6-15/h1-3,5-6,11-12,17-18,22,37H,4,7-10,13-14H2,(H3,25,26)(H,27,35)(H,28,36)(H,29,30)(H,31,34)(H,32,38)/t17-,18+,22?/m1/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| PubMed
| n/a | n/a | 346 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human Factor Xa. |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Plasminogen
(Homo sapiens (Human)) | BDBM50083744
(CHEMBL331807 | N-((R)-3-{[((S)-1-Carbamimidoyl-2-h...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2ccc(=O)[nH]c2)NS(=O)(=O)Cc2ccccc2)C1O Show InChI InChI=1S/C25H34N8O7S/c26-25(27)33-12-4-7-19(24(33)38)31-21(35)14-30-23(37)18(32-41(39,40)15-16-5-2-1-3-6-16)10-11-28-22(36)17-8-9-20(34)29-13-17/h1-3,5-6,8-9,13,18-19,24,32,38H,4,7,10-12,14-15H2,(H3,26,27)(H,28,36)(H,29,34)(H,30,37)(H,31,35)/t18-,19+,24?/m1/s1 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 367 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human thrombolytic protease Plasmin. |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Plasminogen
(Homo sapiens (Human)) | BDBM50083754
(CHEMBL420688 | Pyrazine-2-carboxylic acid ((R)-3-{...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2cnccn2)NS(=O)(=O)Cc2ccccc2)C1O Show InChI InChI=1S/C24H33N9O6S/c25-24(26)33-12-4-7-18(23(33)37)31-20(34)14-30-21(35)17(8-9-29-22(36)19-13-27-10-11-28-19)32-40(38,39)15-16-5-2-1-3-6-16/h1-3,5-6,10-11,13,17-18,23,32,37H,4,7-9,12,14-15H2,(H3,25,26)(H,29,36)(H,30,35)(H,31,34)/t17-,18+,23?/m1/s1 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 521 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human thrombolytic protease Plasmin. |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Prothrombin
(Homo sapiens (Human)) | BDBM50083750
(CHEMBL115902 | Quinoline-3-carboxylic acid ((R)-3-...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2cnc3ccccc3c2)NS(=O)(=O)Cc2ccccc2)C1O Show InChI InChI=1S/C29H36N8O6S/c30-29(31)37-14-6-11-24(28(37)41)35-25(38)17-34-27(40)23(36-44(42,43)18-19-7-2-1-3-8-19)12-13-32-26(39)21-15-20-9-4-5-10-22(20)33-16-21/h1-5,7-10,15-16,23-24,28,36,41H,6,11-14,17-18H2,(H3,30,31)(H,32,39)(H,34,40)(H,35,38)/t23-,24+,28?/m1/s1 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 537 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human Thrombin (FIIa). |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Serine protease 1
(Homo sapiens (Human)) | BDBM50083752
(CHEMBL117678 | N-((R)-3-{[((S)-1-Carbamimidoyl-2-h...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2cccnc2)NS(=O)(=O)Cc2ccccc2)C1O Show InChI InChI=1S/C25H34N8O6S/c26-25(27)33-13-5-9-20(24(33)37)31-21(34)15-30-23(36)19(10-12-29-22(35)18-8-4-11-28-14-18)32-40(38,39)16-17-6-2-1-3-7-17/h1-4,6-8,11,14,19-20,24,32,37H,5,9-10,12-13,15-16H2,(H3,26,27)(H,29,35)(H,30,36)(H,31,34)/t19-,20+,24?/m1/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 561 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human trypsin. |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Plasminogen
(Homo sapiens (Human)) | BDBM50083751
(CHEMBL420322 | Pyrazine-2-carboxylic acid ((R)-4-{...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCCNC(=O)c2cnccn2)NS(=O)(=O)Cc2ccccc2)C1O Show InChI InChI=1S/C25H35N9O6S/c26-25(27)34-13-5-9-19(24(34)38)32-21(35)15-31-22(36)18(33-41(39,40)16-17-6-2-1-3-7-17)8-4-10-30-23(37)20-14-28-11-12-29-20/h1-3,6-7,11-12,14,18-19,24,33,38H,4-5,8-10,13,15-16H2,(H3,26,27)(H,30,37)(H,31,36)(H,32,35)/t18-,19+,24?/m1/s1 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 673 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human thrombolytic protease Plasmin. |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Plasminogen
(Homo sapiens (Human)) | BDBM50083747
(CHEMBL325869 | Cinnoline-4-carboxylic acid ((R)-3-...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2cnnc3ccccc23)NS(=O)(=O)Cc2ccccc2)C1O Show InChI InChI=1S/C28H35N9O6S/c29-28(30)37-14-6-11-23(27(37)41)34-24(38)16-32-26(40)22(36-44(42,43)17-18-7-2-1-3-8-18)12-13-31-25(39)20-15-33-35-21-10-5-4-9-19(20)21/h1-5,7-10,15,22-23,27,36,41H,6,11-14,16-17H2,(H3,29,30)(H,31,39)(H,32,40)(H,34,38)/t22-,23+,27?/m1/s1 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 700 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human thrombolytic protease Plasmin. |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Plasminogen
(Homo sapiens (Human)) | BDBM50083756
(CHEMBL117092 | Isoquinoline-1-carboxylic acid ((R)...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2nccc3ccccc23)NS(=O)(=O)Cc2ccccc2)C1O Show InChI InChI=1S/C29H36N8O6S/c30-29(31)37-16-6-11-23(28(37)41)35-24(38)17-34-26(39)22(36-44(42,43)18-19-7-2-1-3-8-19)13-15-33-27(40)25-21-10-5-4-9-20(21)12-14-32-25/h1-5,7-10,12,14,22-23,28,36,41H,6,11,13,15-18H2,(H3,30,31)(H,33,40)(H,34,39)(H,35,38)/t22-,23+,28?/m1/s1 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 730 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human thrombolytic protease Plasmin. |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Plasminogen
(Homo sapiens (Human)) | BDBM50083745
(5-Bromo-N-((R)-3-{[((S)-1-carbamimidoyl-2-hydroxy-...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2cncc(Br)c2)NS(=O)(=O)Cc2ccccc2)C1O Show InChI InChI=1S/C25H33BrN8O6S/c26-18-11-17(12-29-13-18)22(36)30-9-8-19(33-41(39,40)15-16-5-2-1-3-6-16)23(37)31-14-21(35)32-20-7-4-10-34(24(20)38)25(27)28/h1-3,5-6,11-13,19-20,24,33,38H,4,7-10,14-15H2,(H3,27,28)(H,30,36)(H,31,37)(H,32,35)/t19-,20+,24?/m1/s1 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 1.06E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human thrombolytic protease Plasmin. |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Plasminogen
(Homo sapiens (Human)) | BDBM50083742
(CHEMBL324485 | {(R)-1-{[((S)-1-Carbamimidoyl-2-hyd...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2cnc3ccccc3c2)NC(=O)OCc2ccccc2)C1O Show InChI InChI=1S/C30H36N8O6/c31-29(32)38-14-6-11-24(28(38)42)36-25(39)17-35-27(41)23(37-30(43)44-18-19-7-2-1-3-8-19)12-13-33-26(40)21-15-20-9-4-5-10-22(20)34-16-21/h1-5,7-10,15-16,23-24,28,42H,6,11-14,17-18H2,(H3,31,32)(H,33,40)(H,35,41)(H,36,39)(H,37,43)/t23-,24+,28?/m1/s1 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 1.14E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human thrombolytic protease Plasmin. |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Plasminogen
(Homo sapiens (Human)) | BDBM50083749
(CHEMBL323642 | Pyridine-2-carboxylic acid ((R)-3-{...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2ccccn2)NS(=O)(=O)Cc2ccccc2)C1O Show InChI InChI=1S/C25H34N8O6S/c26-25(27)33-14-6-10-20(24(33)37)31-21(34)15-30-23(36)19(11-13-29-22(35)18-9-4-5-12-28-18)32-40(38,39)16-17-7-2-1-3-8-17/h1-5,7-9,12,19-20,24,32,37H,6,10-11,13-16H2,(H3,26,27)(H,29,35)(H,30,36)(H,31,34)/t19-,20+,24?/m1/s1 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 1.14E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human thrombolytic protease Plasmin. |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Prothrombin
(Homo sapiens (Human)) | BDBM50083746
(CHEMBL117716 | Quinoline-2-carboxylic acid ((R)-3-...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2ccc3ccccc3n2)NS(=O)(=O)Cc2ccccc2)C1O Show InChI InChI=1S/C29H36N8O6S/c30-29(31)37-16-6-11-24(28(37)41)35-25(38)17-33-27(40)23(36-44(42,43)18-19-7-2-1-3-8-19)14-15-32-26(39)22-13-12-20-9-4-5-10-21(20)34-22/h1-5,7-10,12-13,23-24,28,36,41H,6,11,14-18H2,(H3,30,31)(H,32,39)(H,33,40)(H,35,38)/t23-,24+,28?/m1/s1 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 1.27E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human Thrombin (FIIa). |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Plasminogen
(Homo sapiens (Human)) | BDBM50083746
(CHEMBL117716 | Quinoline-2-carboxylic acid ((R)-3-...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2ccc3ccccc3n2)NS(=O)(=O)Cc2ccccc2)C1O Show InChI InChI=1S/C29H36N8O6S/c30-29(31)37-16-6-11-24(28(37)41)35-25(38)17-33-27(40)23(36-44(42,43)18-19-7-2-1-3-8-19)14-15-32-26(39)22-13-12-20-9-4-5-10-21(20)34-22/h1-5,7-10,12-13,23-24,28,36,41H,6,11,14-18H2,(H3,30,31)(H,32,39)(H,33,40)(H,35,38)/t23-,24+,28?/m1/s1 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 1.44E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human thrombolytic protease Plasmin. |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Plasminogen
(Homo sapiens (Human)) | BDBM50083748
(CHEMBL117721 | Pyrazine-2-carboxylic acid ((R)-2-{...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CNC(=O)c2cnccn2)NS(=O)(=O)Cc2ccccc2)C1O Show InChI InChI=1S/C23H31N9O6S/c24-23(25)32-10-4-7-16(22(32)36)30-19(33)13-29-21(35)18(12-28-20(34)17-11-26-8-9-27-17)31-39(37,38)14-15-5-2-1-3-6-15/h1-3,5-6,8-9,11,16,18,22,31,36H,4,7,10,12-14H2,(H3,24,25)(H,28,34)(H,29,35)(H,30,33)/t16-,18+,22?/m0/s1 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 1.48E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human thrombolytic protease Plasmin. |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Prothrombin
(Homo sapiens (Human)) | BDBM50083747
(CHEMBL325869 | Cinnoline-4-carboxylic acid ((R)-3-...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2cnnc3ccccc23)NS(=O)(=O)Cc2ccccc2)C1O Show InChI InChI=1S/C28H35N9O6S/c29-28(30)37-14-6-11-23(27(37)41)34-24(38)16-32-26(40)22(36-44(42,43)17-18-7-2-1-3-8-18)12-13-31-25(39)20-15-33-35-21-10-5-4-9-19(20)21/h1-5,7-10,15,22-23,27,36,41H,6,11-14,16-17H2,(H3,29,30)(H,31,39)(H,32,40)(H,34,38)/t22-,23+,27?/m1/s1 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 1.77E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human Thrombin (FIIa). |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Plasminogen
(Homo sapiens (Human)) | BDBM50083753
(CHEMBL116245 | {(R)-1-{[((S)-1-Carbamimidoyl-2-hyd...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2cnccn2)NC(=O)OCc2ccccc2)C1O Show InChI InChI=1S/C25H33N9O6/c26-24(27)34-12-4-7-18(23(34)38)32-20(35)14-31-21(36)17(8-9-30-22(37)19-13-28-10-11-29-19)33-25(39)40-15-16-5-2-1-3-6-16/h1-3,5-6,10-11,13,17-18,23,38H,4,7-9,12,14-15H2,(H3,26,27)(H,30,37)(H,31,36)(H,32,35)(H,33,39)/t17-,18+,23?/m1/s1 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 2.03E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human thrombolytic protease Plasmin. |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Prothrombin
(Homo sapiens (Human)) | BDBM50083752
(CHEMBL117678 | N-((R)-3-{[((S)-1-Carbamimidoyl-2-h...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2cccnc2)NS(=O)(=O)Cc2ccccc2)C1O Show InChI InChI=1S/C25H34N8O6S/c26-25(27)33-13-5-9-20(24(33)37)31-21(34)15-30-23(36)19(10-12-29-22(35)18-8-4-11-28-14-18)32-40(38,39)16-17-6-2-1-3-7-17/h1-4,6-8,11,14,19-20,24,32,37H,5,9-10,12-13,15-16H2,(H3,26,27)(H,29,35)(H,30,36)(H,31,34)/t19-,20+,24?/m1/s1 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | >2.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human Thrombin (FIIa). |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Serine protease 1
(Homo sapiens (Human)) | BDBM50083738
(CHEMBL115378 | {(R)-1-{[((S)-1-Carbamimidoyl-2-hyd...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2nccc3ccccc23)NC(=O)OCc2ccccc2)C1O Show InChI InChI=1S/C30H36N8O6/c31-29(32)38-16-6-11-23(28(38)42)36-24(39)17-35-26(40)22(37-30(43)44-18-19-7-2-1-3-8-19)13-15-34-27(41)25-21-10-5-4-9-20(21)12-14-33-25/h1-5,7-10,12,14,22-23,28,42H,6,11,13,15-18H2,(H3,31,32)(H,34,41)(H,35,40)(H,36,39)(H,37,43)/t22-,23+,28?/m1/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| PubMed
| n/a | n/a | >2.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human trypsin. |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Prothrombin
(Homo sapiens (Human)) | BDBM50083743
(1N-[1-amino(imino)methyl-6-hydroxy-(5S)-tetrahydro...)Show SMILES NC(=N)NCCCC(NS(=O)(=O)Cc1ccccc1)C(=O)NCC(=O)N[C@H]1CCCN(C1O)C(N)=N Show InChI InChI=1S/C21H35N9O5S/c22-20(23)26-10-4-8-15(29-36(34,35)13-14-6-2-1-3-7-14)18(32)27-12-17(31)28-16-9-5-11-30(19(16)33)21(24)25/h1-3,6-7,15-16,19,29,33H,4-5,8-13H2,(H3,24,25)(H,27,32)(H,28,31)(H4,22,23,26)/t15?,16-,19?/m0/s1 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | >2.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human Thrombin (FIIa). |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Prothrombin
(Homo sapiens (Human)) | BDBM50083755
(3-Hydroxy-quinoxaline-2-carboxylic acid ((R)-3-{[(...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2nc3ccccc3[nH]c2=O)NS(=O)(=O)Cc2ccccc2)C1O Show InChI InChI=1S/C28H35N9O7S/c29-28(30)37-14-6-11-21(27(37)42)33-22(38)15-32-24(39)20(36-45(43,44)16-17-7-2-1-3-8-17)12-13-31-25(40)23-26(41)35-19-10-5-4-9-18(19)34-23/h1-5,7-10,20-21,27,36,42H,6,11-16H2,(H3,29,30)(H,31,40)(H,32,39)(H,33,38)(H,35,41)/t20-,21+,27?/m1/s1 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | >2.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human Thrombin (FIIa). |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50083755
(3-Hydroxy-quinoxaline-2-carboxylic acid ((R)-3-{[(...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2nc3ccccc3[nH]c2=O)NS(=O)(=O)Cc2ccccc2)C1O Show InChI InChI=1S/C28H35N9O7S/c29-28(30)37-14-6-11-21(27(37)42)33-22(38)15-32-24(39)20(36-45(43,44)16-17-7-2-1-3-8-17)12-13-31-25(40)23-26(41)35-19-10-5-4-9-18(19)34-23/h1-5,7-10,20-21,27,36,42H,6,11-16H2,(H3,29,30)(H,31,40)(H,32,39)(H,33,38)(H,35,41)/t20-,21+,27?/m1/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | >2.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human Factor Xa. |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Prothrombin
(Homo sapiens (Human)) | BDBM50083744
(CHEMBL331807 | N-((R)-3-{[((S)-1-Carbamimidoyl-2-h...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2ccc(=O)[nH]c2)NS(=O)(=O)Cc2ccccc2)C1O Show InChI InChI=1S/C25H34N8O7S/c26-25(27)33-12-4-7-19(24(33)38)31-21(35)14-30-23(37)18(32-41(39,40)15-16-5-2-1-3-6-16)10-11-28-22(36)17-8-9-20(34)29-13-17/h1-3,5-6,8-9,13,18-19,24,32,38H,4,7,10-12,14-15H2,(H3,26,27)(H,28,36)(H,29,34)(H,30,37)(H,31,35)/t18-,19+,24?/m1/s1 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | >2.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human Thrombin (FIIa). |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Plasminogen
(Homo sapiens (Human)) | BDBM50083738
(CHEMBL115378 | {(R)-1-{[((S)-1-Carbamimidoyl-2-hyd...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2nccc3ccccc23)NC(=O)OCc2ccccc2)C1O Show InChI InChI=1S/C30H36N8O6/c31-29(32)38-16-6-11-23(28(38)42)36-24(39)17-35-26(40)22(37-30(43)44-18-19-7-2-1-3-8-19)13-15-34-27(41)25-21-10-5-4-9-20(21)12-14-33-25/h1-5,7-10,12,14,22-23,28,42H,6,11,13,15-18H2,(H3,31,32)(H,34,41)(H,35,40)(H,36,39)(H,37,43)/t22-,23+,28?/m1/s1 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| PubMed
| n/a | n/a | >2.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human thrombolytic protease Plasmin. |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Prothrombin
(Homo sapiens (Human)) | BDBM50083740
(((R)-3-[(5-Bromo-pyridine-3-carbonyl)-amino]-1-{[(...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2cncc(Br)c2)NC(=O)OCc2ccccc2)C1O Show InChI InChI=1S/C26H33BrN8O6/c27-18-11-17(12-30-13-18)22(37)31-9-8-19(34-26(40)41-15-16-5-2-1-3-6-16)23(38)32-14-21(36)33-20-7-4-10-35(24(20)39)25(28)29/h1-3,5-6,11-13,19-20,24,39H,4,7-10,14-15H2,(H3,28,29)(H,31,37)(H,32,38)(H,33,36)(H,34,40)/t19-,20+,24?/m1/s1 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | >2.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human Thrombin (FIIa). |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Prothrombin
(Homo sapiens (Human)) | BDBM50083745
(5-Bromo-N-((R)-3-{[((S)-1-carbamimidoyl-2-hydroxy-...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2cncc(Br)c2)NS(=O)(=O)Cc2ccccc2)C1O Show InChI InChI=1S/C25H33BrN8O6S/c26-18-11-17(12-29-13-18)22(36)30-9-8-19(33-41(39,40)15-16-5-2-1-3-6-16)23(37)31-14-21(35)32-20-7-4-10-34(24(20)38)25(27)28/h1-3,5-6,11-13,19-20,24,33,38H,4,7-10,14-15H2,(H3,27,28)(H,30,36)(H,31,37)(H,32,35)/t19-,20+,24?/m1/s1 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | >2.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human Thrombin (FIIa). |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Prothrombin
(Homo sapiens (Human)) | BDBM50083738
(CHEMBL115378 | {(R)-1-{[((S)-1-Carbamimidoyl-2-hyd...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2nccc3ccccc23)NC(=O)OCc2ccccc2)C1O Show InChI InChI=1S/C30H36N8O6/c31-29(32)38-16-6-11-23(28(38)42)36-24(39)17-35-26(40)22(37-30(43)44-18-19-7-2-1-3-8-19)13-15-34-27(41)25-21-10-5-4-9-20(21)12-14-33-25/h1-5,7-10,12,14,22-23,28,42H,6,11,13,15-18H2,(H3,31,32)(H,34,41)(H,35,40)(H,36,39)(H,37,43)/t22-,23+,28?/m1/s1 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| PubMed
| n/a | n/a | >2.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human Thrombin (FIIa). |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Prothrombin
(Homo sapiens (Human)) | BDBM50083749
(CHEMBL323642 | Pyridine-2-carboxylic acid ((R)-3-{...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2ccccn2)NS(=O)(=O)Cc2ccccc2)C1O Show InChI InChI=1S/C25H34N8O6S/c26-25(27)33-14-6-10-20(24(33)37)31-21(34)15-30-23(36)19(11-13-29-22(35)18-9-4-5-12-28-18)32-40(38,39)16-17-7-2-1-3-8-17/h1-5,7-9,12,19-20,24,32,37H,6,10-11,13-16H2,(H3,26,27)(H,29,35)(H,30,36)(H,31,34)/t19-,20+,24?/m1/s1 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | >2.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human Thrombin (FIIa). |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Plasminogen
(Homo sapiens (Human)) | BDBM50083752
(CHEMBL117678 | N-((R)-3-{[((S)-1-Carbamimidoyl-2-h...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2cccnc2)NS(=O)(=O)Cc2ccccc2)C1O Show InChI InChI=1S/C25H34N8O6S/c26-25(27)33-13-5-9-20(24(33)37)31-21(34)15-30-23(36)19(10-12-29-22(35)18-8-4-11-28-14-18)32-40(38,39)16-17-6-2-1-3-7-17/h1-4,6-8,11,14,19-20,24,32,37H,5,9-10,12-13,15-16H2,(H3,26,27)(H,29,35)(H,30,36)(H,31,34)/t19-,20+,24?/m1/s1 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 2.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human thrombolytic protease Plasmin. |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Prothrombin
(Homo sapiens (Human)) | BDBM50083748
(CHEMBL117721 | Pyrazine-2-carboxylic acid ((R)-2-{...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CNC(=O)c2cnccn2)NS(=O)(=O)Cc2ccccc2)C1O Show InChI InChI=1S/C23H31N9O6S/c24-23(25)32-10-4-7-16(22(32)36)30-19(33)13-29-21(35)18(12-28-20(34)17-11-26-8-9-27-17)31-39(37,38)14-15-5-2-1-3-6-15/h1-3,5-6,8-9,11,16,18,22,31,36H,4,7,10,12-14H2,(H3,24,25)(H,28,34)(H,29,35)(H,30,33)/t16-,18+,22?/m0/s1 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | >2.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human Thrombin (FIIa). |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Prothrombin
(Homo sapiens (Human)) | BDBM50083742
(CHEMBL324485 | {(R)-1-{[((S)-1-Carbamimidoyl-2-hyd...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2cnc3ccccc3c2)NC(=O)OCc2ccccc2)C1O Show InChI InChI=1S/C30H36N8O6/c31-29(32)38-14-6-11-24(28(38)42)36-25(39)17-35-27(41)23(37-30(43)44-18-19-7-2-1-3-8-19)12-13-33-26(40)21-15-20-9-4-5-10-22(20)34-16-21/h1-5,7-10,15-16,23-24,28,42H,6,11-14,17-18H2,(H3,31,32)(H,33,40)(H,35,41)(H,36,39)(H,37,43)/t23-,24+,28?/m1/s1 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | >2.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human Thrombin (FIIa). |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Prothrombin
(Homo sapiens (Human)) | BDBM50083754
(CHEMBL420688 | Pyrazine-2-carboxylic acid ((R)-3-{...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2cnccn2)NS(=O)(=O)Cc2ccccc2)C1O Show InChI InChI=1S/C24H33N9O6S/c25-24(26)33-12-4-7-18(23(33)37)31-20(34)14-30-21(35)17(8-9-29-22(36)19-13-27-10-11-28-19)32-40(38,39)15-16-5-2-1-3-6-16/h1-3,5-6,10-11,13,17-18,23,32,37H,4,7-9,12,14-15H2,(H3,25,26)(H,29,36)(H,30,35)(H,31,34)/t17-,18+,23?/m1/s1 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | >2.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human Thrombin (FIIa). |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Prothrombin
(Homo sapiens (Human)) | BDBM50083741
(CHEMBL419222 | {(R)-1-{[((S)-1-Carbamimidoyl-2-hyd...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2cn[nH]c2)NC(=O)OCc2ccccc2)C1O Show InChI InChI=1S/C24H33N9O6/c25-23(26)33-10-4-7-18(22(33)37)31-19(34)13-28-21(36)17(8-9-27-20(35)16-11-29-30-12-16)32-24(38)39-14-15-5-2-1-3-6-15/h1-3,5-6,11-12,17-18,22,37H,4,7-10,13-14H2,(H3,25,26)(H,27,35)(H,28,36)(H,29,30)(H,31,34)(H,32,38)/t17-,18+,22?/m1/s1 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| PubMed
| n/a | n/a | >2.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human Thrombin (FIIa). |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Plasminogen
(Homo sapiens (Human)) | BDBM50083740
(((R)-3-[(5-Bromo-pyridine-3-carbonyl)-amino]-1-{[(...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2cncc(Br)c2)NC(=O)OCc2ccccc2)C1O Show InChI InChI=1S/C26H33BrN8O6/c27-18-11-17(12-30-13-18)22(37)31-9-8-19(34-26(40)41-15-16-5-2-1-3-6-16)23(38)32-14-21(36)33-20-7-4-10-35(24(20)39)25(28)29/h1-3,5-6,11-13,19-20,24,39H,4,7-10,14-15H2,(H3,28,29)(H,31,37)(H,32,38)(H,33,36)(H,34,40)/t19-,20+,24?/m1/s1 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | >2.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human thrombolytic protease Plasmin. |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Prothrombin
(Homo sapiens (Human)) | BDBM50083756
(CHEMBL117092 | Isoquinoline-1-carboxylic acid ((R)...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2nccc3ccccc23)NS(=O)(=O)Cc2ccccc2)C1O Show InChI InChI=1S/C29H36N8O6S/c30-29(31)37-16-6-11-23(28(37)41)35-24(38)17-34-26(39)22(36-44(42,43)18-19-7-2-1-3-8-19)13-15-33-27(40)25-21-10-5-4-9-20(21)12-14-32-25/h1-5,7-10,12,14,22-23,28,36,41H,6,11,13,15-18H2,(H3,30,31)(H,33,40)(H,34,39)(H,35,38)/t22-,23+,28?/m1/s1 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | >2.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human Thrombin (FIIa). |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Plasminogen
(Homo sapiens (Human)) | BDBM50083739
(CHEMBL115707 | {(R)-1-{[((S)-1-Carbamimidoyl-2-hyd...)Show SMILES Cc1cnc(cn1)C(=O)NCC[C@@H](NC(=O)OCc1ccccc1)C(=O)NCC(=O)N[C@H]1CCCN(C1O)C(N)=N Show InChI InChI=1S/C26H35N9O6/c1-16-12-31-20(13-30-16)23(38)29-10-9-18(34-26(40)41-15-17-6-3-2-4-7-17)22(37)32-14-21(36)33-19-8-5-11-35(24(19)39)25(27)28/h2-4,6-7,12-13,18-19,24,39H,5,8-11,14-15H2,1H3,(H3,27,28)(H,29,38)(H,32,37)(H,33,36)(H,34,40)/t18-,19+,24?/m1/s1 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | >2.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human thrombolytic protease Plasmin. |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Prothrombin
(Homo sapiens (Human)) | BDBM50083753
(CHEMBL116245 | {(R)-1-{[((S)-1-Carbamimidoyl-2-hyd...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2cnccn2)NC(=O)OCc2ccccc2)C1O Show InChI InChI=1S/C25H33N9O6/c26-24(27)34-12-4-7-18(23(34)38)32-20(35)14-31-21(36)17(8-9-30-22(37)19-13-28-10-11-29-19)33-25(39)40-15-16-5-2-1-3-6-16/h1-3,5-6,10-11,13,17-18,23,38H,4,7-9,12,14-15H2,(H3,26,27)(H,30,37)(H,31,36)(H,32,35)(H,33,39)/t17-,18+,23?/m1/s1 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 2.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human Thrombin (FIIa). |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Prothrombin
(Homo sapiens (Human)) | BDBM50083751
(CHEMBL420322 | Pyrazine-2-carboxylic acid ((R)-4-{...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCCNC(=O)c2cnccn2)NS(=O)(=O)Cc2ccccc2)C1O Show InChI InChI=1S/C25H35N9O6S/c26-25(27)34-13-5-9-19(24(34)38)32-21(35)15-31-22(36)18(33-41(39,40)16-17-6-2-1-3-7-17)8-4-10-30-23(37)20-14-28-11-12-29-20/h1-3,6-7,11-12,14,18-19,24,33,38H,4-5,8-10,13,15-16H2,(H3,26,27)(H,30,37)(H,31,36)(H,32,35)/t18-,19+,24?/m1/s1 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 2.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human Thrombin (FIIa). |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Prothrombin
(Homo sapiens (Human)) | BDBM50083739
(CHEMBL115707 | {(R)-1-{[((S)-1-Carbamimidoyl-2-hyd...)Show SMILES Cc1cnc(cn1)C(=O)NCC[C@@H](NC(=O)OCc1ccccc1)C(=O)NCC(=O)N[C@H]1CCCN(C1O)C(N)=N Show InChI InChI=1S/C26H35N9O6/c1-16-12-31-20(13-30-16)23(38)29-10-9-18(34-26(40)41-15-17-6-3-2-4-7-17)22(37)32-14-21(36)33-19-8-5-11-35(24(19)39)25(27)28/h2-4,6-7,12-13,18-19,24,39H,5,8-11,14-15H2,1H3,(H3,27,28)(H,29,38)(H,32,37)(H,33,36)(H,34,40)/t18-,19+,24?/m1/s1 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | >2.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human Thrombin (FIIa). |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |
Plasminogen
(Homo sapiens (Human)) | BDBM50083741
(CHEMBL419222 | {(R)-1-{[((S)-1-Carbamimidoyl-2-hyd...)Show SMILES NC(=N)N1CCC[C@H](NC(=O)CNC(=O)[C@@H](CCNC(=O)c2cn[nH]c2)NC(=O)OCc2ccccc2)C1O Show InChI InChI=1S/C24H33N9O6/c25-23(26)33-10-4-7-18(22(33)37)31-19(34)13-28-21(36)17(8-9-27-20(35)16-11-29-30-12-16)32-24(38)39-14-15-5-2-1-3-6-15/h1-3,5-6,11-12,17-18,22,37H,4,7-10,13-14H2,(H3,25,26)(H,27,35)(H,28,36)(H,29,30)(H,31,34)(H,32,38)/t17-,18+,22?/m1/s1 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| PubMed
| n/a | n/a | 3.27E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Corvas International, Inc.
Curated by ChEMBL
| Assay Description In vitro inhibition of human thrombolytic protease Plasmin. |
Bioorg Med Chem Lett 9: 3459-64 (2000)
BindingDB Entry DOI: 10.7270/Q2JD4W1F |
More data for this Ligand-Target Pair | |