Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Kininogen-1' and Ligand = 'BDBM107180'   

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
Kininogen-1 (Homo sapiens (Human))	BDBM107180 (US8592426, 29) Show SMILES Cc1nnc(o1)C(=O)NC1(CC1)C(=O)N[C@H]1CCc2cc(ccc12)-c1cc(Cl)cc(F)c1-c1noc(C)n1 |r| Show InChI InChI=1S/C26H22ClFN6O4/c1-12-29-22(34-38-12)21-18(10-16(27)11-19(21)28)15-3-5-17-14(9-15)4-6-20(17)30-25(36)26(7-8-26)31-23(35)24-33-32-13(2)37-24/h3,5,9-11,20H,4,6-8H2,1-2H3,(H,30,36)(H,31,35)/t20-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	9.5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Hoffmann—La Roche Inc. US Patent					Assay Description Binding assay using Bradykinin-1 receptor.				US Patent US8592426 (2013) BindingDB Entry DOI: 10.7270/Q2WH2NN0
					More data for this Ligand-Target Pair
Kininogen-1 (Homo sapiens (Human))	BDBM107180 (US8592426, 29) Show SMILES Cc1nnc(o1)C(=O)NC1(CC1)C(=O)N[C@H]1CCc2cc(ccc12)-c1cc(Cl)cc(F)c1-c1noc(C)n1 |r| Show InChI InChI=1S/C26H22ClFN6O4/c1-12-29-22(34-38-12)21-18(10-16(27)11-19(21)28)15-3-5-17-14(9-15)4-6-20(17)30-25(36)26(7-8-26)31-23(35)24-33-32-13(2)37-24/h3,5,9-11,20H,4,6-8H2,1-2H3,(H,30,36)(H,31,35)/t20-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	3.40	n/a	n/a	n/a	n/a	n/a	n/a
Hoffmann—La Roche Inc. US Patent					Assay Description Calcium mobilization assay using Bradykinin-1 receptor.				US Patent US8592426 (2013) BindingDB Entry DOI: 10.7270/Q2WH2NN0
					More data for this Ligand-Target Pair