Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Genome polyprotein' and Ligand = 'BDBM50084648'   

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
Genome polyprotein (Hepatitis C virus)	BDBM50084648 (5-[1-[2-(4-Chloro-phenylsulfanyl)-5-nitro-phenyl]-...) Show SMILES [O-][N+](=O)c1ccc(Sc2ccc(Cl)cc2)c(C=C2SC(S)=NC2=O)c1 |w:16.16,c:21| Show InChI InChI=1S/C16H9ClN2O3S3/c17-10-1-4-12(5-2-10)24-13-6-3-11(19(21)22)7-9(13)8-14-15(20)18-16(23)25-14/h1-8H,(H,18,20,23)	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	3.20E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Wollongong Curated by ChEMBL					Assay Description Inhibitory concentration against hepatitis C virus NS3 protease				J Med Chem 48: 1-20 (2005) Article DOI: 10.1021/jm0400101 BindingDB Entry DOI: 10.7270/Q2XP75Q1
					More data for this Ligand-Target Pair
Genome polyprotein (Human rhinovirus B)	BDBM50084648 (5-[1-[2-(4-Chloro-phenylsulfanyl)-5-nitro-phenyl]-...) Show SMILES [O-][N+](=O)c1ccc(Sc2ccc(Cl)cc2)c(C=C2SC(S)=NC2=O)c1 |w:16.16,c:21| Show InChI InChI=1S/C16H9ClN2O3S3/c17-10-1-4-12(5-2-10)24-13-6-3-11(19(21)22)7-9(13)8-14-15(20)18-16(23)25-14/h1-8H,(H,18,20,23)	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	3.20E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Queensland Curated by ChEMBL					Assay Description Inhibitory concentration against Protease				J Med Chem 43: 305-41 (2000) Checked by Author BindingDB Entry DOI: 10.7270/Q2JD4XH4
					More data for this Ligand-Target Pair