Found 41 hits Enz. Inhib. hit(s) with all data for entry = 50035107 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)) | BDBM50085518
(Cyclic urea 2,4-diazepin-3-one analogue | bis(2,2,...)Show SMILES NC(=[NH2+])c1cccc(c1)N1CCCCN(C2CCN(CC2)S(=O)(=O)Cc2ccccn2)C1=O Show InChI InChI=1S/C23H30N6O3S/c24-22(25)18-6-5-8-21(16-18)29-13-4-3-12-28(23(29)30)20-9-14-27(15-10-20)33(31,32)17-19-7-1-2-11-26-19/h1-2,5-8,11,16,20H,3-4,9-10,12-15,17H2,(H3,24,25)/p+1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Similars
| PubMed
| 10 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
DuPont Pharmaceuticals Company
Curated by ChEMBL
| Assay Description Inhibition of coagulation factor Xa |
Bioorg Med Chem Lett 10: 301-4 (2000)
BindingDB Entry DOI: 10.7270/Q2639Q7R |
More data for this Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50085511
(CHEMBL103993 | Cyclic urea 2,4-diazepin-3-one anal...)Show SMILES NC(=[NH2+])c1cccc(c1)N1CCCCN(C2CCN(CC2)S(=O)(=O)Cc2ccccc2)C1=O Show InChI InChI=1S/C24H31N5O3S/c25-23(26)20-9-6-10-22(17-20)29-14-5-4-13-28(24(29)30)21-11-15-27(16-12-21)33(31,32)18-19-7-2-1-3-8-19/h1-3,6-10,17,21H,4-5,11-16,18H2,(H3,25,26)/p+1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| 10 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
DuPont Pharmaceuticals Company
Curated by ChEMBL
| Assay Description Inhibition of coagulation factor Xa |
Bioorg Med Chem Lett 10: 301-4 (2000)
BindingDB Entry DOI: 10.7270/Q2639Q7R |
More data for this Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50085509
(CHEMBL104995 | Cyclic urea 2,4-diazepin-3-one anal...)Show SMILES NC(=[NH2+])c1cccc(c1)N1CCCCN(C2CCN(CC2)S(=O)(=O)c2cccs2)C1=O Show InChI InChI=1S/C21H27N5O3S2/c22-20(23)16-5-3-6-18(15-16)26-11-2-1-10-25(21(26)27)17-8-12-24(13-9-17)31(28,29)19-7-4-14-30-19/h3-7,14-15,17H,1-2,8-13H2,(H3,22,23)/p+1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| 12 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
DuPont Pharmaceuticals Company
Curated by ChEMBL
| Assay Description Inhibition of coagulation factor Xa |
Bioorg Med Chem Lett 10: 301-4 (2000)
BindingDB Entry DOI: 10.7270/Q2639Q7R |
More data for this Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50085523
(Cyclic urea 2,4-diazepin-3-one analogue | bis(2,2,...)Show SMILES NC(=[NH2+])c1cccc(c1)N1CCCCN(C2CCN(Cc3ccccn3)CC2)C1=O Show InChI InChI=1S/C23H30N6O/c24-22(25)18-6-5-8-21(16-18)29-13-4-3-12-28(23(29)30)20-9-14-27(15-10-20)17-19-7-1-2-11-26-19/h1-2,5-8,11,16,20H,3-4,9-10,12-15,17H2,(H3,24,25)/p+1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Similars
| PubMed
| 12 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
DuPont Pharmaceuticals Company
Curated by ChEMBL
| Assay Description Inhibition of coagulation factor Xa |
Bioorg Med Chem Lett 10: 301-4 (2000)
BindingDB Entry DOI: 10.7270/Q2639Q7R |
More data for this Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50085519
(CHEMBL102502 | Cyclic urea 2,4-diazepin-3-one anal...)Show SMILES NC(=[NH2+])c1cccc(c1)N1CCCCN(C2CCN(CC2)S(=O)(=O)c2ccccc2)C1=O Show InChI InChI=1S/C23H29N5O3S/c24-22(25)18-7-6-8-20(17-18)28-14-5-4-13-27(23(28)29)19-11-15-26(16-12-19)32(30,31)21-9-2-1-3-10-21/h1-3,6-10,17,19H,4-5,11-16H2,(H3,24,25)/p+1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| 24 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
DuPont Pharmaceuticals Company
Curated by ChEMBL
| Assay Description Inhibition of coagulation factor Xa |
Bioorg Med Chem Lett 10: 301-4 (2000)
BindingDB Entry DOI: 10.7270/Q2639Q7R |
More data for this Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50085515
(Cyclic urea 2,4-diazepin-3-one analogue | bis(2,2,...)Show SMILES NC(=[NH2+])c1cccc(c1)N1CCCCN(C2CCN(CC2)S(=O)(=O)c2ccccc2N)C1=O Show InChI InChI=1S/C23H30N6O3S/c24-20-8-1-2-9-21(20)33(31,32)27-14-10-18(11-15-27)28-12-3-4-13-29(23(28)30)19-7-5-6-17(16-19)22(25)26/h1-2,5-9,16,18H,3-4,10-15,24H2,(H3,25,26)/p+1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Similars
| PubMed
| 34 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
DuPont Pharmaceuticals Company
Curated by ChEMBL
| Assay Description Inhibition of coagulation factor Xa |
Bioorg Med Chem Lett 10: 301-4 (2000)
BindingDB Entry DOI: 10.7270/Q2639Q7R |
More data for this Ligand-Target Pair | |
Serine protease 1
(Homo sapiens (Human)) | BDBM50085509
(CHEMBL104995 | Cyclic urea 2,4-diazepin-3-one anal...)Show SMILES NC(=[NH2+])c1cccc(c1)N1CCCCN(C2CCN(CC2)S(=O)(=O)c2cccs2)C1=O Show InChI InChI=1S/C21H27N5O3S2/c22-20(23)16-5-3-6-18(15-16)26-11-2-1-10-25(21(26)27)17-8-12-24(13-9-17)31(28,29)19-7-4-14-30-19/h3-7,14-15,17H,1-2,8-13H2,(H3,22,23)/p+1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| 52 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
DuPont Pharmaceuticals Company
Curated by ChEMBL
| Assay Description Inhibitory activity against trypsin |
Bioorg Med Chem Lett 10: 301-4 (2000)
BindingDB Entry DOI: 10.7270/Q2639Q7R |
More data for this Ligand-Target Pair | |
Serine protease 1
(Homo sapiens (Human)) | BDBM50085518
(Cyclic urea 2,4-diazepin-3-one analogue | bis(2,2,...)Show SMILES NC(=[NH2+])c1cccc(c1)N1CCCCN(C2CCN(CC2)S(=O)(=O)Cc2ccccn2)C1=O Show InChI InChI=1S/C23H30N6O3S/c24-22(25)18-6-5-8-21(16-18)29-13-4-3-12-28(23(29)30)20-9-14-27(15-10-20)33(31,32)17-19-7-1-2-11-26-19/h1-2,5-8,11,16,20H,3-4,9-10,12-15,17H2,(H3,24,25)/p+1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| PC cid PC sid UniChem
Similars
| PubMed
| 57 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
DuPont Pharmaceuticals Company
Curated by ChEMBL
| Assay Description Inhibitory activity against trypsin |
Bioorg Med Chem Lett 10: 301-4 (2000)
BindingDB Entry DOI: 10.7270/Q2639Q7R |
More data for this Ligand-Target Pair | |
Serine protease 1
(Homo sapiens (Human)) | BDBM50085519
(CHEMBL102502 | Cyclic urea 2,4-diazepin-3-one anal...)Show SMILES NC(=[NH2+])c1cccc(c1)N1CCCCN(C2CCN(CC2)S(=O)(=O)c2ccccc2)C1=O Show InChI InChI=1S/C23H29N5O3S/c24-22(25)18-7-6-8-20(17-18)28-14-5-4-13-27(23(28)29)19-11-15-26(16-12-19)32(30,31)21-9-2-1-3-10-21/h1-3,6-10,17,19H,4-5,11-16H2,(H3,24,25)/p+1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| 60 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
DuPont Pharmaceuticals Company
Curated by ChEMBL
| Assay Description Inhibitory activity against trypsin |
Bioorg Med Chem Lett 10: 301-4 (2000)
BindingDB Entry DOI: 10.7270/Q2639Q7R |
More data for this Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50085512
(Cyclic urea 2,4-diazepin-3-one analogue | bis(2,2,...)Show SMILES NC(=[NH2+])c1cccc(c1)N1CCCCN(C2CCN(CC2)S(=O)(=O)c2ccc(N)cc2)C1=O Show InChI InChI=1S/C23H30N6O3S/c24-18-6-8-21(9-7-18)33(31,32)27-14-10-19(11-15-27)28-12-1-2-13-29(23(28)30)20-5-3-4-17(16-20)22(25)26/h3-9,16,19H,1-2,10-15,24H2,(H3,25,26)/p+1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Similars
| PubMed
| 71 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
DuPont Pharmaceuticals Company
Curated by ChEMBL
| Assay Description Inhibition of coagulation factor Xa |
Bioorg Med Chem Lett 10: 301-4 (2000)
BindingDB Entry DOI: 10.7270/Q2639Q7R |
More data for this Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50085514
(3-[2-Oxo-3-(1-thiophen-2-ylmethyl-piperidin-4-yl)-...)Show SMILES NC(=[NH2+])c1cccc(c1)N1CCCCN(C2CCN(Cc3cccs3)CC2)C1=O Show InChI InChI=1S/C22H29N5OS/c23-21(24)17-5-3-6-19(15-17)27-11-2-1-10-26(22(27)28)18-8-12-25(13-9-18)16-20-7-4-14-29-20/h3-7,14-15,18H,1-2,8-13,16H2,(H3,23,24)/p+1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| PubMed
| 80 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
DuPont Pharmaceuticals Company
Curated by ChEMBL
| Assay Description Inhibition of coagulation factor Xa |
Bioorg Med Chem Lett 10: 301-4 (2000)
BindingDB Entry DOI: 10.7270/Q2639Q7R |
More data for this Ligand-Target Pair | |
Serine protease 1
(Homo sapiens (Human)) | BDBM50085511
(CHEMBL103993 | Cyclic urea 2,4-diazepin-3-one anal...)Show SMILES NC(=[NH2+])c1cccc(c1)N1CCCCN(C2CCN(CC2)S(=O)(=O)Cc2ccccc2)C1=O Show InChI InChI=1S/C24H31N5O3S/c25-23(26)20-9-6-10-22(17-20)29-14-5-4-13-28(24(29)30)21-11-15-27(16-12-21)33(31,32)18-19-7-2-1-3-8-19/h1-3,6-10,17,21H,4-5,11-16,18H2,(H3,25,26)/p+1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| 80 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
DuPont Pharmaceuticals Company
Curated by ChEMBL
| Assay Description Inhibitory activity against trypsin |
Bioorg Med Chem Lett 10: 301-4 (2000)
BindingDB Entry DOI: 10.7270/Q2639Q7R |
More data for this Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50085521
(CHEMBL553840 | Cyclic urea 2,4-diazepin-3-one anal...)Show SMILES NC(=[NH2+])c1cccc(c1)N1CCCCN(C2CCN(Cc3ccccc3)CC2)C1=O Show InChI InChI=1S/C24H31N5O/c25-23(26)20-9-6-10-22(17-20)29-14-5-4-13-28(24(29)30)21-11-15-27(16-12-21)18-19-7-2-1-3-8-19/h1-3,6-10,17,21H,4-5,11-16,18H2,(H3,25,26)/p+1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| 102 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
DuPont Pharmaceuticals Company
Curated by ChEMBL
| Assay Description Inhibition of coagulation factor Xa |
Bioorg Med Chem Lett 10: 301-4 (2000)
BindingDB Entry DOI: 10.7270/Q2639Q7R |
More data for this Ligand-Target Pair | |
Serine protease 1
(Homo sapiens (Human)) | BDBM50085523
(Cyclic urea 2,4-diazepin-3-one analogue | bis(2,2,...)Show SMILES NC(=[NH2+])c1cccc(c1)N1CCCCN(C2CCN(Cc3ccccn3)CC2)C1=O Show InChI InChI=1S/C23H30N6O/c24-22(25)18-6-5-8-21(16-18)29-13-4-3-12-28(23(29)30)20-9-14-27(15-10-20)17-19-7-1-2-11-26-19/h1-2,5-8,11,16,20H,3-4,9-10,12-15,17H2,(H3,24,25)/p+1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| PC cid PC sid UniChem
Similars
| PubMed
| 120 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
DuPont Pharmaceuticals Company
Curated by ChEMBL
| Assay Description Inhibitory activity against trypsin |
Bioorg Med Chem Lett 10: 301-4 (2000)
BindingDB Entry DOI: 10.7270/Q2639Q7R |
More data for this Ligand-Target Pair | |
Serine protease 1
(Homo sapiens (Human)) | BDBM50085515
(Cyclic urea 2,4-diazepin-3-one analogue | bis(2,2,...)Show SMILES NC(=[NH2+])c1cccc(c1)N1CCCCN(C2CCN(CC2)S(=O)(=O)c2ccccc2N)C1=O Show InChI InChI=1S/C23H30N6O3S/c24-20-8-1-2-9-21(20)33(31,32)27-14-10-18(11-15-27)28-12-3-4-13-29(23(28)30)19-7-5-6-17(16-19)22(25)26/h1-2,5-9,16,18H,3-4,10-15,24H2,(H3,25,26)/p+1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| PC cid PC sid UniChem
Similars
| PubMed
| 130 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
DuPont Pharmaceuticals Company
Curated by ChEMBL
| Assay Description Inhibitory activity against trypsin |
Bioorg Med Chem Lett 10: 301-4 (2000)
BindingDB Entry DOI: 10.7270/Q2639Q7R |
More data for this Ligand-Target Pair | |
Serine protease 1
(Homo sapiens (Human)) | BDBM50085514
(3-[2-Oxo-3-(1-thiophen-2-ylmethyl-piperidin-4-yl)-...)Show SMILES NC(=[NH2+])c1cccc(c1)N1CCCCN(C2CCN(Cc3cccs3)CC2)C1=O Show InChI InChI=1S/C22H29N5OS/c23-21(24)17-5-3-6-19(15-17)27-11-2-1-10-26(22(27)28)18-8-12-25(13-9-18)16-20-7-4-14-29-20/h3-7,14-15,18H,1-2,8-13,16H2,(H3,23,24)/p+1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| PubMed
| 170 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
DuPont Pharmaceuticals Company
Curated by ChEMBL
| Assay Description Inhibitory activity against trypsin |
Bioorg Med Chem Lett 10: 301-4 (2000)
BindingDB Entry DOI: 10.7270/Q2639Q7R |
More data for this Ligand-Target Pair | |
Serine protease 1
(Homo sapiens (Human)) | BDBM50085512
(Cyclic urea 2,4-diazepin-3-one analogue | bis(2,2,...)Show SMILES NC(=[NH2+])c1cccc(c1)N1CCCCN(C2CCN(CC2)S(=O)(=O)c2ccc(N)cc2)C1=O Show InChI InChI=1S/C23H30N6O3S/c24-18-6-8-21(9-7-18)33(31,32)27-14-10-19(11-15-27)28-12-1-2-13-29(23(28)30)20-5-3-4-17(16-20)22(25)26/h3-9,16,19H,1-2,10-15,24H2,(H3,25,26)/p+1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| PC cid PC sid UniChem
Similars
| PubMed
| 190 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
DuPont Pharmaceuticals Company
Curated by ChEMBL
| Assay Description Inhibitory activity against trypsin |
Bioorg Med Chem Lett 10: 301-4 (2000)
BindingDB Entry DOI: 10.7270/Q2639Q7R |
More data for this Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50085522
(Cyclic urea 2,4-diazepin-3-one analogue | bis(2,2,...)Show SMILES NC(=[NH2+])c1cccc(c1)N1CCCCN(C2CCN(CC2)S(=O)(=O)c2cccc(N)c2)C1=O Show InChI InChI=1S/C23H30N6O3S/c24-18-6-4-8-21(16-18)33(31,32)27-13-9-19(10-14-27)28-11-1-2-12-29(23(28)30)20-7-3-5-17(15-20)22(25)26/h3-8,15-16,19H,1-2,9-14,24H2,(H3,25,26)/p+1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Similars
| PubMed
| 200 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
DuPont Pharmaceuticals Company
Curated by ChEMBL
| Assay Description Inhibition of coagulation factor Xa |
Bioorg Med Chem Lett 10: 301-4 (2000)
BindingDB Entry DOI: 10.7270/Q2639Q7R |
More data for this Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50085516
(Cyclic urea 2,4-diazepin-3-one analogue | bis(2,2,...)Show SMILES NC(=[NH2+])c1cccc(c1)N1CCCCN(C2CCN(Cc3ccncc3)CC2)C1=O Show InChI InChI=1S/C23H30N6O/c24-22(25)19-4-3-5-21(16-19)29-13-2-1-12-28(23(29)30)20-8-14-27(15-9-20)17-18-6-10-26-11-7-18/h3-7,10-11,16,20H,1-2,8-9,12-15,17H2,(H3,24,25)/p+1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Similars
| PubMed
| 200 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
DuPont Pharmaceuticals Company
Curated by ChEMBL
| Assay Description Inhibition of coagulation factor Xa |
Bioorg Med Chem Lett 10: 301-4 (2000)
BindingDB Entry DOI: 10.7270/Q2639Q7R |
More data for this Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50085517
(CHEMBL556200 | Cyclic urea 2,4-diazepin-3-one anal...)Show SMILES NC(=[NH2+])c1cccc(c1)N1CCCCN(C2CCN(CCc3ccccc3)CC2)C1=O Show InChI InChI=1S/C25H33N5O/c26-24(27)21-9-6-10-23(19-21)30-15-5-4-14-29(25(30)31)22-12-17-28(18-13-22)16-11-20-7-2-1-3-8-20/h1-3,6-10,19,22H,4-5,11-18H2,(H3,26,27)/p+1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| 220 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
DuPont Pharmaceuticals Company
Curated by ChEMBL
| Assay Description Inhibition of coagulation factor Xa |
Bioorg Med Chem Lett 10: 301-4 (2000)
BindingDB Entry DOI: 10.7270/Q2639Q7R |
More data for this Ligand-Target Pair | |
Serine protease 1
(Homo sapiens (Human)) | BDBM50085521
(CHEMBL553840 | Cyclic urea 2,4-diazepin-3-one anal...)Show SMILES NC(=[NH2+])c1cccc(c1)N1CCCCN(C2CCN(Cc3ccccc3)CC2)C1=O Show InChI InChI=1S/C24H31N5O/c25-23(26)20-9-6-10-22(17-20)29-14-5-4-13-28(24(29)30)21-11-15-27(16-12-21)18-19-7-2-1-3-8-19/h1-3,6-10,17,21H,4-5,11-16,18H2,(H3,25,26)/p+1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| 282 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
DuPont Pharmaceuticals Company
Curated by ChEMBL
| Assay Description Inhibitory activity against trypsin |
Bioorg Med Chem Lett 10: 301-4 (2000)
BindingDB Entry DOI: 10.7270/Q2639Q7R |
More data for this Ligand-Target Pair | |
Prothrombin
(Homo sapiens (Human)) | BDBM50085511
(CHEMBL103993 | Cyclic urea 2,4-diazepin-3-one anal...)Show SMILES NC(=[NH2+])c1cccc(c1)N1CCCCN(C2CCN(CC2)S(=O)(=O)Cc2ccccc2)C1=O Show InChI InChI=1S/C24H31N5O3S/c25-23(26)20-9-6-10-22(17-20)29-14-5-4-13-28(24(29)30)21-11-15-27(16-12-21)33(31,32)18-19-7-2-1-3-8-19/h1-3,6-10,17,21H,4-5,11-16,18H2,(H3,25,26)/p+1 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| 500 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
DuPont Pharmaceuticals Company
Curated by ChEMBL
| Assay Description Inhibitory activity against thrombin |
Bioorg Med Chem Lett 10: 301-4 (2000)
BindingDB Entry DOI: 10.7270/Q2639Q7R |
More data for this Ligand-Target Pair | |
Prothrombin
(Homo sapiens (Human)) | BDBM50085518
(Cyclic urea 2,4-diazepin-3-one analogue | bis(2,2,...)Show SMILES NC(=[NH2+])c1cccc(c1)N1CCCCN(C2CCN(CC2)S(=O)(=O)Cc2ccccn2)C1=O Show InChI InChI=1S/C23H30N6O3S/c24-22(25)18-6-5-8-21(16-18)29-13-4-3-12-28(23(29)30)20-9-14-27(15-10-20)33(31,32)17-19-7-1-2-11-26-19/h1-2,5-8,11,16,20H,3-4,9-10,12-15,17H2,(H3,24,25)/p+1 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Similars
| PubMed
| 500 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
DuPont Pharmaceuticals Company
Curated by ChEMBL
| Assay Description Inhibitory activity against thrombin |
Bioorg Med Chem Lett 10: 301-4 (2000)
BindingDB Entry DOI: 10.7270/Q2639Q7R |
More data for this Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50085510
(Cyclic urea 2,4-diazepin-3-one analogue | bis(2,2,...)Show SMILES NC(=[NH2+])c1cccc(c1)N1CCCCN(C2CCN(Cc3cccnc3)CC2)C1=O Show InChI InChI=1S/C23H30N6O/c24-22(25)19-6-3-7-21(15-19)29-12-2-1-11-28(23(29)30)20-8-13-27(14-9-20)17-18-5-4-10-26-16-18/h3-7,10,15-16,20H,1-2,8-9,11-14,17H2,(H3,24,25)/p+1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Similars
| PubMed
| 670 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
DuPont Pharmaceuticals Company
Curated by ChEMBL
| Assay Description Inhibition of coagulation factor Xa |
Bioorg Med Chem Lett 10: 301-4 (2000)
BindingDB Entry DOI: 10.7270/Q2639Q7R |
More data for this Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50085520
(CHEMBL432783 | Cyclic urea 2,4-diazepin-3-one anal...)Show SMILES NC(=[NH2+])c1ccc(cc1)N1CCCCN(c2cccc(c2)C(N)=[NH2+])C1=O Show InChI InChI=1S/C19H22N6O/c20-17(21)13-6-8-15(9-7-13)24-10-1-2-11-25(19(24)26)16-5-3-4-14(12-16)18(22)23/h3-9,12H,1-2,10-11H2,(H3,20,21)(H3,22,23)/p+2 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| 800 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
DuPont Pharmaceuticals Company
Curated by ChEMBL
| Assay Description Inhibition of coagulation factor Xa |
Bioorg Med Chem Lett 10: 301-4 (2000)
BindingDB Entry DOI: 10.7270/Q2639Q7R |
More data for this Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50085524
(CHEMBL102578 | Cyclic urea 2,4-diazepin-3-one anal...)Show SMILES NC(=[NH2+])c1cccc(c1)N1CCCCN(C2CCN(CC2)C(=O)Cc2ccccc2)C1=O Show InChI InChI=1S/C25H31N5O2/c26-24(27)20-9-6-10-22(18-20)30-14-5-4-13-29(25(30)32)21-11-15-28(16-12-21)23(31)17-19-7-2-1-3-8-19/h1-3,6-10,18,21H,4-5,11-17H2,(H3,26,27)/p+1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| 900 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
DuPont Pharmaceuticals Company
Curated by ChEMBL
| Assay Description Inhibition of coagulation factor Xa |
Bioorg Med Chem Lett 10: 301-4 (2000)
BindingDB Entry DOI: 10.7270/Q2639Q7R |
More data for this Ligand-Target Pair | |
Serine protease 1
(Homo sapiens (Human)) | BDBM50085517
(CHEMBL556200 | Cyclic urea 2,4-diazepin-3-one anal...)Show SMILES NC(=[NH2+])c1cccc(c1)N1CCCCN(C2CCN(CCc3ccccc3)CC2)C1=O Show InChI InChI=1S/C25H33N5O/c26-24(27)21-9-6-10-23(19-21)30-15-5-4-14-29(25(30)31)22-12-17-28(18-13-22)16-11-20-7-2-1-3-8-20/h1-3,6-10,19,22H,4-5,11-18H2,(H3,26,27)/p+1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| 1.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
DuPont Pharmaceuticals Company
Curated by ChEMBL
| Assay Description Inhibitory activity against trypsin |
Bioorg Med Chem Lett 10: 301-4 (2000)
BindingDB Entry DOI: 10.7270/Q2639Q7R |
More data for this Ligand-Target Pair | |
Prothrombin
(Homo sapiens (Human)) | BDBM50085514
(3-[2-Oxo-3-(1-thiophen-2-ylmethyl-piperidin-4-yl)-...)Show SMILES NC(=[NH2+])c1cccc(c1)N1CCCCN(C2CCN(Cc3cccs3)CC2)C1=O Show InChI InChI=1S/C22H29N5OS/c23-21(24)17-5-3-6-19(15-17)27-11-2-1-10-26(22(27)28)18-8-12-25(13-9-18)16-20-7-4-14-29-20/h3-7,14-15,18H,1-2,8-13,16H2,(H3,23,24)/p+1 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| PubMed
| 1.40E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
DuPont Pharmaceuticals Company
Curated by ChEMBL
| Assay Description Inhibitory activity against thrombin |
Bioorg Med Chem Lett 10: 301-4 (2000)
BindingDB Entry DOI: 10.7270/Q2639Q7R |
More data for this Ligand-Target Pair | |
Prothrombin
(Homo sapiens (Human)) | BDBM50085509
(CHEMBL104995 | Cyclic urea 2,4-diazepin-3-one anal...)Show SMILES NC(=[NH2+])c1cccc(c1)N1CCCCN(C2CCN(CC2)S(=O)(=O)c2cccs2)C1=O Show InChI InChI=1S/C21H27N5O3S2/c22-20(23)16-5-3-6-18(15-16)26-11-2-1-10-25(21(26)27)17-8-12-24(13-9-17)31(28,29)19-7-4-14-30-19/h3-7,14-15,17H,1-2,8-13H2,(H3,22,23)/p+1 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| 1.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
DuPont Pharmaceuticals Company
Curated by ChEMBL
| Assay Description Inhibitory activity against thrombin |
Bioorg Med Chem Lett 10: 301-4 (2000)
BindingDB Entry DOI: 10.7270/Q2639Q7R |
More data for this Ligand-Target Pair | |
Prothrombin
(Homo sapiens (Human)) | BDBM50085519
(CHEMBL102502 | Cyclic urea 2,4-diazepin-3-one anal...)Show SMILES NC(=[NH2+])c1cccc(c1)N1CCCCN(C2CCN(CC2)S(=O)(=O)c2ccccc2)C1=O Show InChI InChI=1S/C23H29N5O3S/c24-22(25)18-7-6-8-20(17-18)28-14-5-4-13-27(23(28)29)19-11-15-26(16-12-19)32(30,31)21-9-2-1-3-10-21/h1-3,6-10,17,19H,4-5,11-16H2,(H3,24,25)/p+1 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| 1.60E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
DuPont Pharmaceuticals Company
Curated by ChEMBL
| Assay Description Inhibitory activity against thrombin |
Bioorg Med Chem Lett 10: 301-4 (2000)
BindingDB Entry DOI: 10.7270/Q2639Q7R |
More data for this Ligand-Target Pair | |
Prothrombin
(Homo sapiens (Human)) | BDBM50085521
(CHEMBL553840 | Cyclic urea 2,4-diazepin-3-one anal...)Show SMILES NC(=[NH2+])c1cccc(c1)N1CCCCN(C2CCN(Cc3ccccc3)CC2)C1=O Show InChI InChI=1S/C24H31N5O/c25-23(26)20-9-6-10-22(17-20)29-14-5-4-13-28(24(29)30)21-11-15-27(16-12-21)18-19-7-2-1-3-8-19/h1-3,6-10,17,21H,4-5,11-16,18H2,(H3,25,26)/p+1 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| 2.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
DuPont Pharmaceuticals Company
Curated by ChEMBL
| Assay Description Inhibitory activity against thrombin |
Bioorg Med Chem Lett 10: 301-4 (2000)
BindingDB Entry DOI: 10.7270/Q2639Q7R |
More data for this Ligand-Target Pair | |
Prothrombin
(Homo sapiens (Human)) | BDBM50085522
(Cyclic urea 2,4-diazepin-3-one analogue | bis(2,2,...)Show SMILES NC(=[NH2+])c1cccc(c1)N1CCCCN(C2CCN(CC2)S(=O)(=O)c2cccc(N)c2)C1=O Show InChI InChI=1S/C23H30N6O3S/c24-18-6-4-8-21(16-18)33(31,32)27-13-9-19(10-14-27)28-11-1-2-12-29(23(28)30)20-7-3-5-17(15-20)22(25)26/h3-8,15-16,19H,1-2,9-14,24H2,(H3,25,26)/p+1 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Similars
| PubMed
| 2.20E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
DuPont Pharmaceuticals Company
Curated by ChEMBL
| Assay Description Inhibitory activity against thrombin |
Bioorg Med Chem Lett 10: 301-4 (2000)
BindingDB Entry DOI: 10.7270/Q2639Q7R |
More data for this Ligand-Target Pair | |
Prothrombin
(Homo sapiens (Human)) | BDBM50085515
(Cyclic urea 2,4-diazepin-3-one analogue | bis(2,2,...)Show SMILES NC(=[NH2+])c1cccc(c1)N1CCCCN(C2CCN(CC2)S(=O)(=O)c2ccccc2N)C1=O Show InChI InChI=1S/C23H30N6O3S/c24-20-8-1-2-9-21(20)33(31,32)27-14-10-18(11-15-27)28-12-3-4-13-29(23(28)30)19-7-5-6-17(16-19)22(25)26/h1-2,5-9,16,18H,3-4,10-15,24H2,(H3,25,26)/p+1 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Similars
| PubMed
| 2.40E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
DuPont Pharmaceuticals Company
Curated by ChEMBL
| Assay Description Inhibitory activity against thrombin |
Bioorg Med Chem Lett 10: 301-4 (2000)
BindingDB Entry DOI: 10.7270/Q2639Q7R |
More data for this Ligand-Target Pair | |
Prothrombin
(Homo sapiens (Human)) | BDBM50085523
(Cyclic urea 2,4-diazepin-3-one analogue | bis(2,2,...)Show SMILES NC(=[NH2+])c1cccc(c1)N1CCCCN(C2CCN(Cc3ccccn3)CC2)C1=O Show InChI InChI=1S/C23H30N6O/c24-22(25)18-6-5-8-21(16-18)29-13-4-3-12-28(23(29)30)20-9-14-27(15-10-20)17-19-7-1-2-11-26-19/h1-2,5-8,11,16,20H,3-4,9-10,12-15,17H2,(H3,24,25)/p+1 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Similars
| PubMed
| 2.60E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
DuPont Pharmaceuticals Company
Curated by ChEMBL
| Assay Description Inhibitory activity against thrombin |
Bioorg Med Chem Lett 10: 301-4 (2000)
BindingDB Entry DOI: 10.7270/Q2639Q7R |
More data for this Ligand-Target Pair | |
Prothrombin
(Homo sapiens (Human)) | BDBM50085517
(CHEMBL556200 | Cyclic urea 2,4-diazepin-3-one anal...)Show SMILES NC(=[NH2+])c1cccc(c1)N1CCCCN(C2CCN(CCc3ccccc3)CC2)C1=O Show InChI InChI=1S/C25H33N5O/c26-24(27)21-9-6-10-23(19-21)30-15-5-4-14-29(25(30)31)22-12-17-28(18-13-22)16-11-20-7-2-1-3-8-20/h1-3,6-10,19,22H,4-5,11-18H2,(H3,26,27)/p+1 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| 3.60E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
DuPont Pharmaceuticals Company
Curated by ChEMBL
| Assay Description Inhibitory activity against thrombin |
Bioorg Med Chem Lett 10: 301-4 (2000)
BindingDB Entry DOI: 10.7270/Q2639Q7R |
More data for this Ligand-Target Pair | |
Prothrombin
(Homo sapiens (Human)) | BDBM50085510
(Cyclic urea 2,4-diazepin-3-one analogue | bis(2,2,...)Show SMILES NC(=[NH2+])c1cccc(c1)N1CCCCN(C2CCN(Cc3cccnc3)CC2)C1=O Show InChI InChI=1S/C23H30N6O/c24-22(25)19-6-3-7-21(15-19)29-12-2-1-11-28(23(29)30)20-8-13-27(14-9-20)17-18-5-4-10-26-16-18/h3-7,10,15-16,20H,1-2,8-9,11-14,17H2,(H3,24,25)/p+1 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Similars
| PubMed
| 5.30E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
DuPont Pharmaceuticals Company
Curated by ChEMBL
| Assay Description Inhibitory activity against thrombin |
Bioorg Med Chem Lett 10: 301-4 (2000)
BindingDB Entry DOI: 10.7270/Q2639Q7R |
More data for this Ligand-Target Pair | |
Prothrombin
(Homo sapiens (Human)) | BDBM50085512
(Cyclic urea 2,4-diazepin-3-one analogue | bis(2,2,...)Show SMILES NC(=[NH2+])c1cccc(c1)N1CCCCN(C2CCN(CC2)S(=O)(=O)c2ccc(N)cc2)C1=O Show InChI InChI=1S/C23H30N6O3S/c24-18-6-8-21(9-7-18)33(31,32)27-14-10-19(11-15-27)28-12-1-2-13-29(23(28)30)20-5-3-4-17(16-20)22(25)26/h3-9,16,19H,1-2,10-15,24H2,(H3,25,26)/p+1 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Similars
| PubMed
| 6.30E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
DuPont Pharmaceuticals Company
Curated by ChEMBL
| Assay Description Inhibitory activity against thrombin |
Bioorg Med Chem Lett 10: 301-4 (2000)
BindingDB Entry DOI: 10.7270/Q2639Q7R |
More data for this Ligand-Target Pair | |
Prothrombin
(Homo sapiens (Human)) | BDBM50085516
(Cyclic urea 2,4-diazepin-3-one analogue | bis(2,2,...)Show SMILES NC(=[NH2+])c1cccc(c1)N1CCCCN(C2CCN(Cc3ccncc3)CC2)C1=O Show InChI InChI=1S/C23H30N6O/c24-22(25)19-4-3-5-21(16-19)29-13-2-1-12-28(23(29)30)20-8-14-27(15-9-20)17-18-6-10-26-11-7-18/h3-7,10-11,16,20H,1-2,8-9,12-15,17H2,(H3,24,25)/p+1 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Similars
| PubMed
| 6.80E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
DuPont Pharmaceuticals Company
Curated by ChEMBL
| Assay Description Inhibitory activity against thrombin |
Bioorg Med Chem Lett 10: 301-4 (2000)
BindingDB Entry DOI: 10.7270/Q2639Q7R |
More data for this Ligand-Target Pair | |
Coagulation factor X
(Homo sapiens (Human)) | BDBM50085513
(CHEMBL101586 | Cyclic urea 2,4-diazepin-3-one anal...)Show SMILES NC(=[NH2+])c1cccc(c1)N1CCCCN(C2CCN(CC2)C(=O)c2ccccc2)C1=O Show InChI InChI=1S/C24H29N5O2/c25-22(26)19-9-6-10-21(17-19)29-14-5-4-13-28(24(29)31)20-11-15-27(16-12-20)23(30)18-7-2-1-3-8-18/h1-3,6-10,17,20H,4-5,11-16H2,(H3,25,26)/p+1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| 7.80E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
DuPont Pharmaceuticals Company
Curated by ChEMBL
| Assay Description Inhibition of coagulation factor Xa |
Bioorg Med Chem Lett 10: 301-4 (2000)
BindingDB Entry DOI: 10.7270/Q2639Q7R |
More data for this Ligand-Target Pair | |
Prothrombin
(Homo sapiens (Human)) | BDBM50085524
(CHEMBL102578 | Cyclic urea 2,4-diazepin-3-one anal...)Show SMILES NC(=[NH2+])c1cccc(c1)N1CCCCN(C2CCN(CC2)C(=O)Cc2ccccc2)C1=O Show InChI InChI=1S/C25H31N5O2/c26-24(27)20-9-6-10-22(18-20)30-14-5-4-13-29(25(30)32)21-11-15-28(16-12-21)23(31)17-19-7-2-1-3-8-19/h1-3,6-10,18,21H,4-5,11-17H2,(H3,26,27)/p+1 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| 1.18E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
DuPont Pharmaceuticals Company
Curated by ChEMBL
| Assay Description Inhibitory activity against thrombin |
Bioorg Med Chem Lett 10: 301-4 (2000)
BindingDB Entry DOI: 10.7270/Q2639Q7R |
More data for this Ligand-Target Pair | |
Prothrombin
(Homo sapiens (Human)) | BDBM50085513
(CHEMBL101586 | Cyclic urea 2,4-diazepin-3-one anal...)Show SMILES NC(=[NH2+])c1cccc(c1)N1CCCCN(C2CCN(CC2)C(=O)c2ccccc2)C1=O Show InChI InChI=1S/C24H29N5O2/c25-22(26)19-9-6-10-21(17-19)29-14-5-4-13-28(24(29)31)20-11-15-27(16-12-20)23(30)18-7-2-1-3-8-18/h1-3,6-10,17,20H,4-5,11-16H2,(H3,25,26)/p+1 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| >2.10E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
DuPont Pharmaceuticals Company
Curated by ChEMBL
| Assay Description Inhibitory activity against thrombin |
Bioorg Med Chem Lett 10: 301-4 (2000)
BindingDB Entry DOI: 10.7270/Q2639Q7R |
More data for this Ligand-Target Pair | |