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SMILES: CCOCCN(CCOCC)c1cc(cc(n1)-c1ccc(O)c(C)c1)-c1ccccc1

InChI Key: InChIKey=UDUZAKDLZAVSDS-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50102198   

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))	BDBM50102198 (4-{6-[Bis-(2-ethoxy-ethyl)-amino]-4-phenyl-pyridin...) Show SMILES CCOCCN(CCOCC)c1cc(cc(n1)-c1ccc(O)c(C)c1)-c1ccccc1 Show InChI InChI=1S/C26H32N2O3/c1-4-30-15-13-28(14-16-31-5-2)26-19-23(21-9-7-6-8-10-21)18-24(27-26)22-11-12-25(29)20(3)17-22/h6-12,17-19,29H,4-5,13-16H2,1-3H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	1.17E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Glaxo Wellcome Research and Development Curated by ChEMBL					Assay Description Ability to displace [3H]-17-beta-estradiol from Estrogen receptor beta by scintillation proximity assay.				Bioorg Med Chem Lett 11: 1939-42 (2001) BindingDB Entry DOI: 10.7270/Q2ZK5FZ0
					More data for this Ligand-Target Pair
Estrogen receptor (Homo sapiens (Human))	BDBM50102198 (4-{6-[Bis-(2-ethoxy-ethyl)-amino]-4-phenyl-pyridin...) Show SMILES CCOCCN(CCOCC)c1cc(cc(n1)-c1ccc(O)c(C)c1)-c1ccccc1 Show InChI InChI=1S/C26H32N2O3/c1-4-30-15-13-28(14-16-31-5-2)26-19-23(21-9-7-6-8-10-21)18-24(27-26)22-11-12-25(29)20(3)17-22/h6-12,17-19,29H,4-5,13-16H2,1-3H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	2.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Glaxo Wellcome Research and Development Curated by ChEMBL					Assay Description Ability to displace [3H]-17-beta-estradiol from Estrogen receptor alpha by scintillation proximity assay.				Bioorg Med Chem Lett 11: 1939-42 (2001) BindingDB Entry DOI: 10.7270/Q2ZK5FZ0
					More data for this Ligand-Target Pair