Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Progesterone receptor' and Ligand = 'BDBM50298035'   

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
Progesterone receptor (Homo sapiens (Human))	BDBM50298035 ((S)-2-chloro-4-((2-chlorobenzyl)(1-(pyridin-2-ylme...) Show SMILES Clc1ccccc1CN([C@H]1CCN(Cc2ccccn2)C1)c1ccc(C#N)c(Cl)c1 |r| Show InChI InChI=1S/C24H22Cl2N4/c25-23-7-2-1-5-19(23)15-30(21-9-8-18(14-27)24(26)13-21)22-10-12-29(17-22)16-20-6-3-4-11-28-20/h1-9,11,13,22H,10,12,15-17H2/t22-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	20	n/a	n/a	n/a	n/a	n/a	n/a
GlaxoSmithKline Pharmaceuticals Curated by ChEMBL					Assay Description Binding affinity to PR by fluorescence polarization based competition binding assay				Bioorg Med Chem Lett 19: 4777-80 (2009) Article DOI: 10.1016/j.bmcl.2009.06.055 BindingDB Entry DOI: 10.7270/Q2TB16XG
					More data for this Ligand-Target Pair
Progesterone receptor (Homo sapiens (Human))	BDBM50298035 ((S)-2-chloro-4-((2-chlorobenzyl)(1-(pyridin-2-ylme...) Show SMILES Clc1ccccc1CN([C@H]1CCN(Cc2ccccn2)C1)c1ccc(C#N)c(Cl)c1 |r| Show InChI InChI=1S/C24H22Cl2N4/c25-23-7-2-1-5-19(23)15-30(21-9-8-18(14-27)24(26)13-21)22-10-12-29(17-22)16-20-6-3-4-11-28-20/h1-9,11,13,22H,10,12,15-17H2/t22-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a
GlaxoSmithKline Pharmaceuticals Curated by ChEMBL					Assay Description Agonist activity at PR expressed in african green monkey CV-1 cells by luciferase reporter assay				Bioorg Med Chem Lett 19: 4777-80 (2009) Article DOI: 10.1016/j.bmcl.2009.06.055 BindingDB Entry DOI: 10.7270/Q2TB16XG
					More data for this Ligand-Target Pair