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SMILES: CN(CCc1ccccc1)c1cc(cc(n1)-c1ccc(O)cc1)-c1ccccc1C

InChI Key: InChIKey=PNRRSDWBCUPCNL-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50102202   

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 (Homo sapiens (Human))	BDBM50102202 (4-[6-(Methyl-phenethyl-amino)-4-o-tolyl-pyridin-2-...) Show SMILES CN(CCc1ccccc1)c1cc(cc(n1)-c1ccc(O)cc1)-c1ccccc1C Show InChI InChI=1S/C27H26N2O/c1-20-8-6-7-11-25(20)23-18-26(22-12-14-24(30)15-13-22)28-27(19-23)29(2)17-16-21-9-4-3-5-10-21/h3-15,18-19,30H,16-17H2,1-2H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	650	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
Estrogen receptor beta (Homo sapiens (Human))	BDBM50102202 (4-[6-(Methyl-phenethyl-amino)-4-o-tolyl-pyridin-2-...) Show SMILES CN(CCc1ccccc1)c1cc(cc(n1)-c1ccc(O)cc1)-c1ccccc1C Show InChI InChI=1S/C27H26N2O/c1-20-8-6-7-11-25(20)23-18-26(22-12-14-24(30)15-13-22)28-27(19-23)29(2)17-16-21-9-4-3-5-10-21/h3-15,18-19,30H,16-17H2,1-2H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	1.10E+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