Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Genome polyprotein' and Ligand = 'BDBM50112655'   

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 (Human rhinovirus B)	BDBM50112655 (4-[(Naphthalene-2-carbonyl)-amino]-5-(2-oxo-pyrrol...) Show SMILES CCOC(=O)\C=C\[C@H](C[C@@H]1CCNC1=O)NC(=O)c1ccc2ccccc2c1 |r| Show InChI InChI=1S/C22H24N2O4/c1-2-28-20(25)10-9-19(14-18-11-12-23-21(18)26)24-22(27)17-8-7-15-5-3-4-6-16(15)13-17/h3-10,13,18-19H,2,11-12,14H2,1H3,(H,23,26)(H,24,27)/b10-9+/t18-,19+/m0/s1	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	n/a	n/a	1.40E+3	n/a	n/a	n/a	n/a
Pfizer Global R&D-La Jolla/Agouron Pharmaceuticals Curated by ChEMBL					Assay Description 50% effective concentration required to inhibit Human Rhinovirus 2 Protease 3C				J Med Chem 45: 2016-23 (2002) BindingDB Entry DOI: 10.7270/Q289156B
					More data for this Ligand-Target Pair
Genome polyprotein (Human rhinovirus B)	BDBM50112655 (4-[(Naphthalene-2-carbonyl)-amino]-5-(2-oxo-pyrrol...) Show SMILES CCOC(=O)\C=C\[C@H](C[C@@H]1CCNC1=O)NC(=O)c1ccc2ccccc2c1 |r| Show InChI InChI=1S/C22H24N2O4/c1-2-28-20(25)10-9-19(14-18-11-12-23-21(18)26)24-22(27)17-8-7-15-5-3-4-6-16(15)13-17/h3-10,13,18-19H,2,11-12,14H2,1H3,(H,23,26)(H,24,27)/b10-9+/t18-,19+/m0/s1	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	n/a	n/a	150	n/a	n/a	n/a	n/a
Pfizer Global R&D-La Jolla/Agouron Pharmaceuticals Curated by ChEMBL					Assay Description Inhibition of Human Rhinovirus 14 (HRV14) Protease 3C				J Med Chem 45: 2016-23 (2002) BindingDB Entry DOI: 10.7270/Q289156B
					More data for this Ligand-Target Pair