Compile Data Set for Download or QSAR

Found 4 hits Enz. Inhib. hit(s) with Target = 'Progesterone receptor' and Ligand = 'BDBM50049490'   

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))	BDBM50049490 (Acetic acid 5-bromo-4-methoxy-2-(4,6,6-trimethyl-2...) Show SMILES COc1cc(CC2C(=C)C=C(C)CC2(C)C)c(OC(C)=O)cc1Br |t:9| Show InChI InChI=1S/C20H25BrO3/c1-12-7-13(2)16(20(4,5)11-12)8-15-9-19(23-6)17(21)10-18(15)24-14(3)22/h7,9-10,16H,2,8,11H2,1,3-6H3	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	60	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Ligand Pharmaceuticals, Inc. Curated by ChEMBL					Assay Description Binding affinity determined for human Progesterone receptor A isoform				J Med Chem 39: 1778-89 (1996) Article DOI: 10.1021/jm950747d BindingDB Entry DOI: 10.7270/Q2416XQ2
					More data for this Ligand-Target Pair
Progesterone receptor (Homo sapiens (Human))	BDBM50049490 (Acetic acid 5-bromo-4-methoxy-2-(4,6,6-trimethyl-2...) Show SMILES COc1cc(CC2C(=C)C=C(C)CC2(C)C)c(OC(C)=O)cc1Br |t:9| Show InChI InChI=1S/C20H25BrO3/c1-12-7-13(2)16(20(4,5)11-12)8-15-9-19(23-6)17(21)10-18(15)24-14(3)22/h7,9-10,16H,2,8,11H2,1,3-6H3	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	710	n/a	n/a	n/a	n/a	n/a	n/a
Ligand Pharmaceuticals, Inc. Curated by ChEMBL					Assay Description Concentration required to give half-maximal inhibition against human Progesterone receptor B isoform in co-transfected CV-1 cell lines.				J Med Chem 39: 1778-89 (1996) Article DOI: 10.1021/jm950747d BindingDB Entry DOI: 10.7270/Q2416XQ2
					More data for this Ligand-Target Pair
Progesterone receptor (Homo sapiens (Human))	BDBM50049490 (Acetic acid 5-bromo-4-methoxy-2-(4,6,6-trimethyl-2...) Show SMILES COc1cc(CC2C(=C)C=C(C)CC2(C)C)c(OC(C)=O)cc1Br |t:9| Show InChI InChI=1S/C20H25BrO3/c1-12-7-13(2)16(20(4,5)11-12)8-15-9-19(23-6)17(21)10-18(15)24-14(3)22/h7,9-10,16H,2,8,11H2,1,3-6H3	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	770	n/a	n/a	n/a	n/a	n/a	n/a
Ligand Pharmaceuticals, Inc. Curated by ChEMBL					Assay Description Antagonistic potency to the human progesterone receptor measured in the T-47D alkaline phosphatase assay				J Med Chem 39: 1778-89 (1996) Article DOI: 10.1021/jm950747d BindingDB Entry DOI: 10.7270/Q2416XQ2
					More data for this Ligand-Target Pair
Progesterone receptor (Homo sapiens (Human))	BDBM50049490 (Acetic acid 5-bromo-4-methoxy-2-(4,6,6-trimethyl-2...) Show SMILES COc1cc(CC2C(=C)C=C(C)CC2(C)C)c(OC(C)=O)cc1Br |t:9| Show InChI InChI=1S/C20H25BrO3/c1-12-7-13(2)16(20(4,5)11-12)8-15-9-19(23-6)17(21)10-18(15)24-14(3)22/h7,9-10,16H,2,8,11H2,1,3-6H3	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	1.46E+3	n/a	n/a	n/a	n/a
Ligand Pharmaceuticals, Inc. Curated by ChEMBL					Assay Description Effective concentration against human Progesterone receptor B isoform expressed in CV-1 cells				J Med Chem 39: 1778-89 (1996) Article DOI: 10.1021/jm950747d BindingDB Entry DOI: 10.7270/Q2416XQ2
					More data for this Ligand-Target Pair