Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'C-C chemokine receptor type 5' and Ligand = 'BDBM50205736'   

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
C-C chemokine receptor type 5 (Homo sapiens (Human))	BDBM50205736 (2-(4-benzyl-5-(2-(piperidin-1-yl)ethyl)-4H-1,2,4-t...) Show SMILES Cc1ccc(NC(=O)CSc2nnc(CCN3CCCCC3)n2Cc2ccccc2)c(C)c1 Show InChI InChI=1S/C26H33N5OS/c1-20-11-12-23(21(2)17-20)27-25(32)19-33-26-29-28-24(13-16-30-14-7-4-8-15-30)31(26)18-22-9-5-3-6-10-22/h3,5-6,9-12,17H,4,7-8,13-16,18-19H2,1-2H3,(H,27,32)	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.70E+4	n/a	n/a	n/a	n/a	n/a	n/a
CNRS UMR 7175-LC1 Curated by ChEMBL					Assay Description Displacement of [125I]MIP1beta from CCR5 expressed in CHO-K1 cells				J Med Chem 50: 1294-303 (2007) Article DOI: 10.1021/jm061389p BindingDB Entry DOI: 10.7270/Q2KD1XK6
					More data for this Ligand-Target Pair
C-C chemokine receptor type 5 (Homo sapiens (Human))	BDBM50205736 (2-(4-benzyl-5-(2-(piperidin-1-yl)ethyl)-4H-1,2,4-t...) Show SMILES Cc1ccc(NC(=O)CSc2nnc(CCN3CCCCC3)n2Cc2ccccc2)c(C)c1 Show InChI InChI=1S/C26H33N5OS/c1-20-11-12-23(21(2)17-20)27-25(32)19-33-26-29-28-24(13-16-30-14-7-4-8-15-30)31(26)18-22-9-5-3-6-10-22/h3,5-6,9-12,17H,4,7-8,13-16,18-19H2,1-2H3,(H,27,32)	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	3.00E+3	n/a	n/a	n/a	n/a
CNRS UMR 7175-LC1 Curated by ChEMBL					Assay Description Agonist activity at CCR5 expressed in CHO-K1 cells in aqeuorin based assay				J Med Chem 50: 1294-303 (2007) Article DOI: 10.1021/jm061389p BindingDB Entry DOI: 10.7270/Q2KD1XK6
					More data for this Ligand-Target Pair