Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'C-C chemokine receptor type 1' and Ligand = 'BDBM50436261'   

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 1 (Homo sapiens (Human))	BDBM50436261 (CHEMBL2398764) Show SMILES CC(C)[C@@H](NC(=O)c1cccc(c1)-c1ccccc1NC(N)=O)C(=O)N1CCC(CC1)c1ccc(Cl)cc1 |r| Show InChI InChI=1S/C30H33ClN4O3/c1-19(2)27(29(37)35-16-14-21(15-17-35)20-10-12-24(31)13-11-20)34-28(36)23-7-5-6-22(18-23)25-8-3-4-9-26(25)33-30(32)38/h3-13,18-19,21,27H,14-17H2,1-2H3,(H,34,36)(H3,32,33,38)/t27-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.80	n/a	n/a	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Company Curated by ChEMBL					Assay Description Binding affinity to human CCR1				Bioorg Med Chem Lett 23: 3833-40 (2013) Article DOI: 10.1016/j.bmcl.2013.04.079 BindingDB Entry DOI: 10.7270/Q24X596G
					More data for this Ligand-Target Pair
C-C chemokine receptor type 1 (Homo sapiens (Human))	BDBM50436261 (CHEMBL2398764) Show SMILES CC(C)[C@@H](NC(=O)c1cccc(c1)-c1ccccc1NC(N)=O)C(=O)N1CCC(CC1)c1ccc(Cl)cc1 |r| Show InChI InChI=1S/C30H33ClN4O3/c1-19(2)27(29(37)35-16-14-21(15-17-35)20-10-12-24(31)13-11-20)34-28(36)23-7-5-6-22(18-23)25-8-3-4-9-26(25)33-30(32)38/h3-13,18-19,21,27H,14-17H2,1-2H3,(H,34,36)(H3,32,33,38)/t27-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	153	n/a	n/a	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Company Curated by ChEMBL					Assay Description Antagonist activity at human CCR1 assessed as inhibition of MIP1alpha-induced chemotaxis				Bioorg Med Chem Lett 23: 3833-40 (2013) Article DOI: 10.1016/j.bmcl.2013.04.079 BindingDB Entry DOI: 10.7270/Q24X596G
					More data for this Ligand-Target Pair