null

SMILES: CCOC(=O)N1CCc2cc(O)ccc2C1c1ccc(OCCN2CCCC2)cc1

InChI Key: InChIKey=KUEZQAQZOUTJKW-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50146219   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kcal/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Estrogen receptor beta (Homo sapiens (Human))	BDBM50146219 (6-Hydroxy-1-[4-(2-pyrrolidin-1-yl-ethoxy)-phenyl]-...) Show SMILES CCOC(=O)N1CCc2cc(O)ccc2C1c1ccc(OCCN2CCCC2)cc1 Show InChI InChI=1S/C24H30N2O4/c1-2-29-24(28)26-14-11-19-17-20(27)7-10-22(19)23(26)18-5-8-21(9-6-18)30-16-15-25-12-3-4-13-25/h5-10,17,23,27H,2-4,11-16H2,1H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	293	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer Global Research and Development Curated by ChEMBL					Assay Description In vitro concentration required to inhibit [3H]-estradiol binding to human estrogen receptor beta expressed in 293T cells				Bioorg Med Chem Lett 14: 2729-33 (2004) Article DOI: 10.1016/j.bmcl.2004.03.077 BindingDB Entry DOI: 10.7270/Q2J67GBK
					More data for this Ligand-Target Pair
Estrogen receptor (Homo sapiens (Human))	BDBM50146219 (6-Hydroxy-1-[4-(2-pyrrolidin-1-yl-ethoxy)-phenyl]-...) Show SMILES CCOC(=O)N1CCc2cc(O)ccc2C1c1ccc(OCCN2CCCC2)cc1 Show InChI InChI=1S/C24H30N2O4/c1-2-29-24(28)26-14-11-19-17-20(27)7-10-22(19)23(26)18-5-8-21(9-6-18)30-16-15-25-12-3-4-13-25/h5-10,17,23,27H,2-4,11-16H2,1H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	44	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer Global Research and Development Curated by ChEMBL					Assay Description In vitro concentration required to inhibit [3H]-estradiol binding to human estrogen receptor alpha expressed in 293T cells				Bioorg Med Chem Lett 14: 2729-33 (2004) Article DOI: 10.1016/j.bmcl.2004.03.077 BindingDB Entry DOI: 10.7270/Q2J67GBK
					More data for this Ligand-Target Pair