Compile Data Set for Download or QSAR

Found 3 hits of ki for monomerid = 50098555   

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
Suppressor of tumorigenicity 14 protein (Homo sapiens (Human))	BDBM50098555 (4-[6-(4-Carbamimidoyl-phenoxy)-hexyloxy]-3-iodo-be...) Show SMILES NC(=N)c1ccc(OCCCCCCOc2ccc(cc2I)C(N)=N)cc1 Show InChI InChI=1S/C20H25IN4O2/c21-17-13-15(20(24)25)7-10-18(17)27-12-4-2-1-3-11-26-16-8-5-14(6-9-16)19(22)23/h5-10,13H,1-4,11-12H2,(H3,22,23)(H3,24,25)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	191	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Georgetown University Medical Center Curated by ChEMBL					Assay Description compound was tested for inhibitory activity against Matriptase				J Med Chem 44: 1349-55 (2001) BindingDB Entry DOI: 10.7270/Q2057F62
					More data for this Ligand-Target Pair
Prothrombin (Homo sapiens (Human))	BDBM50098555 (4-[6-(4-Carbamimidoyl-phenoxy)-hexyloxy]-3-iodo-be...) Show SMILES NC(=N)c1ccc(OCCCCCCOc2ccc(cc2I)C(N)=N)cc1 Show InChI InChI=1S/C20H25IN4O2/c21-17-13-15(20(24)25)7-10-18(17)27-12-4-2-1-3-11-26-16-8-5-14(6-9-16)19(22)23/h5-10,13H,1-4,11-12H2,(H3,22,23)(H3,24,25)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	796	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Georgetown University Medical Center Curated by ChEMBL					Assay Description compound was tested for inhibitory activity against Thrombin				J Med Chem 44: 1349-55 (2001) BindingDB Entry DOI: 10.7270/Q2057F62
					More data for this Ligand-Target Pair
Urokinase-type plasminogen activator (Homo sapiens (Human))	BDBM50098555 (4-[6-(4-Carbamimidoyl-phenoxy)-hexyloxy]-3-iodo-be...) Show SMILES NC(=N)c1ccc(OCCCCCCOc2ccc(cc2I)C(N)=N)cc1 Show InChI InChI=1S/C20H25IN4O2/c21-17-13-15(20(24)25)7-10-18(17)27-12-4-2-1-3-11-26-16-8-5-14(6-9-16)19(22)23/h5-10,13H,1-4,11-12H2,(H3,22,23)(H3,24,25)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	1.98E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Georgetown University Medical Center Curated by ChEMBL					Assay Description compound was tested for inhibitory activity against Urokinase-type plasminogen activator(microPa)				J Med Chem 44: 1349-55 (2001) BindingDB Entry DOI: 10.7270/Q2057F62
					More data for this Ligand-Target Pair