Compile Data Set for Download or QSAR

Found 4 hits of ki for monomerid = 50069145   

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 VII (Homo sapiens (Human))	BDBM50069145 (2-[3-(3-Amino-phenyl)-5-benzyl-[1,2,4]triazol-1-yl...) Show SMILES [H][C@@]12C[C@@]([H])(C1(C)C)[C@]1(C)OB(O[C@]1([H])C2)[C@H](CCCCN)NC(=O)Cn1nc(nc1Cc1ccccc1)-c1cccc(N)c1 Show InChI InChI=1S/C32H43BN6O3/c1-31(2)23-18-25(31)32(3)26(19-23)41-33(42-32)27(14-7-8-15-34)36-29(40)20-39-28(16-21-10-5-4-6-11-21)37-30(38-39)22-12-9-13-24(35)17-22/h4-6,9-13,17,23,25-27H,7-8,14-16,18-20,34-35H2,1-3H3,(H,36,40)/t23-,25-,26+,27-,32-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	150	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
DuPont Merck Pharmaceutical Company Curated by ChEMBL					Assay Description Inhibition against human Coagulation factor VII				Bioorg Med Chem Lett 8: 775-80 (1999) BindingDB Entry DOI: 10.7270/Q2P84B1P
					More data for this Ligand-Target Pair
Prothrombin (Homo sapiens (Human))	BDBM50069145 (2-[3-(3-Amino-phenyl)-5-benzyl-[1,2,4]triazol-1-yl...) Show SMILES [H][C@@]12C[C@@]([H])(C1(C)C)[C@]1(C)OB(O[C@]1([H])C2)[C@H](CCCCN)NC(=O)Cn1nc(nc1Cc1ccccc1)-c1cccc(N)c1 Show InChI InChI=1S/C32H43BN6O3/c1-31(2)23-18-25(31)32(3)26(19-23)41-33(42-32)27(14-7-8-15-34)36-29(40)20-39-28(16-21-10-5-4-6-11-21)37-30(38-39)22-12-9-13-24(35)17-22/h4-6,9-13,17,23,25-27H,7-8,14-16,18-20,34-35H2,1-3H3,(H,36,40)/t23-,25-,26+,27-,32-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	150	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
DuPont Merck Pharmaceutical Company Curated by ChEMBL					Assay Description Inhibition against human thrombin				Bioorg Med Chem Lett 8: 775-80 (1999) BindingDB Entry DOI: 10.7270/Q2P84B1P
					More data for this Ligand-Target Pair
Serine protease 1 (Homo sapiens (Human))	BDBM50069145 (2-[3-(3-Amino-phenyl)-5-benzyl-[1,2,4]triazol-1-yl...) Show SMILES [H][C@@]12C[C@@]([H])(C1(C)C)[C@]1(C)OB(O[C@]1([H])C2)[C@H](CCCCN)NC(=O)Cn1nc(nc1Cc1ccccc1)-c1cccc(N)c1 Show InChI InChI=1S/C32H43BN6O3/c1-31(2)23-18-25(31)32(3)26(19-23)41-33(42-32)27(14-7-8-15-34)36-29(40)20-39-28(16-21-10-5-4-6-11-21)37-30(38-39)22-12-9-13-24(35)17-22/h4-6,9-13,17,23,25-27H,7-8,14-16,18-20,34-35H2,1-3H3,(H,36,40)/t23-,25-,26+,27-,32-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	150	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
DuPont Merck Pharmaceutical Company Curated by ChEMBL					Assay Description Inhibition of trypsin				Bioorg Med Chem Lett 8: 775-80 (1999) BindingDB Entry DOI: 10.7270/Q2P84B1P
					More data for this Ligand-Target Pair
Coagulation factor X (Homo sapiens (Human))	BDBM50069145 (2-[3-(3-Amino-phenyl)-5-benzyl-[1,2,4]triazol-1-yl...) Show SMILES [H][C@@]12C[C@@]([H])(C1(C)C)[C@]1(C)OB(O[C@]1([H])C2)[C@H](CCCCN)NC(=O)Cn1nc(nc1Cc1ccccc1)-c1cccc(N)c1 Show InChI InChI=1S/C32H43BN6O3/c1-31(2)23-18-25(31)32(3)26(19-23)41-33(42-32)27(14-7-8-15-34)36-29(40)20-39-28(16-21-10-5-4-6-11-21)37-30(38-39)22-12-9-13-24(35)17-22/h4-6,9-13,17,23,25-27H,7-8,14-16,18-20,34-35H2,1-3H3,(H,36,40)/t23-,25-,26+,27-,32-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	>6.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
DuPont Merck Pharmaceutical Company Curated by ChEMBL					Assay Description Inhibition against human coagulation factor Xa				Bioorg Med Chem Lett 8: 775-80 (1999) BindingDB Entry DOI: 10.7270/Q2P84B1P
					More data for this Ligand-Target Pair