null

SMILES: CN(CCc1ccccc1)c1cc(cc(n1)-c1ccc(O)cc1)-c1ccc(O)cc1

InChI Key: InChIKey=SEAGICQGKLIWII-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50102192   

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))	BDBM50102192 (4-[4-(4-hydroxyphenyl)-6-methyl(phenethyl)amino-2-...) Show SMILES CN(CCc1ccccc1)c1cc(cc(n1)-c1ccc(O)cc1)-c1ccc(O)cc1 Show InChI InChI=1S/C26H24N2O2/c1-28(16-15-19-5-3-2-4-6-19)26-18-22(20-7-11-23(29)12-8-20)17-25(27-26)21-9-13-24(30)14-10-21/h2-14,17-18,29-30H,15-16H2,1H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	>3.00E+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 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))	BDBM50102192 (4-[4-(4-hydroxyphenyl)-6-methyl(phenethyl)amino-2-...) Show SMILES CN(CCc1ccccc1)c1cc(cc(n1)-c1ccc(O)cc1)-c1ccc(O)cc1 Show InChI InChI=1S/C26H24N2O2/c1-28(16-15-19-5-3-2-4-6-19)26-18-22(20-7-11-23(29)12-8-20)17-25(27-26)21-9-13-24(30)14-10-21/h2-14,17-18,29-30H,15-16H2,1H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	>3.00E+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