Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Progesterone receptor' and Ligand = 'BDBM50298213'   

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))	BDBM50298213 ((S)-2-chloro-4-((2,3-difluorobenzyl)(1-methyl-5-ox...) Show SMILES CN1C[C@H](CC1=O)N(Cc1cccc(F)c1F)c1ccc(C#N)c(Cl)c1 |r| Show InChI InChI=1S/C19H16ClF2N3O/c1-24-11-15(8-18(24)26)25(10-13-3-2-4-17(21)19(13)22)14-6-5-12(9-23)16(20)7-14/h2-7,15H,8,10-11H2,1H3/t15-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	25	n/a	n/a	n/a	n/a	n/a	n/a
GlaxoSmithKline Pharmaceuticals Curated by ChEMBL					Assay Description Binding affinity to progesterone receptor				Bioorg Med Chem Lett 19: 4664-8 (2009) Article DOI: 10.1016/j.bmcl.2009.06.081 BindingDB Entry DOI: 10.7270/Q25H7G9T
					More data for this Ligand-Target Pair
Progesterone receptor (Homo sapiens (Human))	BDBM50298213 ((S)-2-chloro-4-((2,3-difluorobenzyl)(1-methyl-5-ox...) Show SMILES CN1C[C@H](CC1=O)N(Cc1cccc(F)c1F)c1ccc(C#N)c(Cl)c1 |r| Show InChI InChI=1S/C19H16ClF2N3O/c1-24-11-15(8-18(24)26)25(10-13-3-2-4-17(21)19(13)22)14-6-5-12(9-23)16(20)7-14/h2-7,15H,8,10-11H2,1H3/t15-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	n/a	n/a	35	n/a	n/a	n/a	n/a
GlaxoSmithKline Pharmaceuticals Curated by ChEMBL					Assay Description Agonist activity at progesterone receptor in human T47D cells assessed as inhibition of progesterone-induced alkaline phosphatase activity				Bioorg Med Chem Lett 19: 4664-8 (2009) Article DOI: 10.1016/j.bmcl.2009.06.081 BindingDB Entry DOI: 10.7270/Q25H7G9T
					More data for this Ligand-Target Pair