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

InChI Key: InChIKey=QDCUXSGHOJHXPC-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50102200   

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))	BDBM50102200 (4-[6-(Butyl-methyl-amino)-4-phenyl-pyridin-2-yl]-2...) Show SMILES CCCCN(C)c1cc(cc(n1)-c1ccc(O)c(C)c1)-c1ccccc1 Show InChI InChI=1S/C23H26N2O/c1-4-5-13-25(3)23-16-20(18-9-7-6-8-10-18)15-21(24-23)19-11-12-22(26)17(2)14-19/h6-12,14-16,26H,4-5,13H2,1-3H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	660	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))	BDBM50102200 (4-[6-(Butyl-methyl-amino)-4-phenyl-pyridin-2-yl]-2...) Show SMILES CCCCN(C)c1cc(cc(n1)-c1ccc(O)c(C)c1)-c1ccccc1 Show InChI InChI=1S/C23H26N2O/c1-4-5-13-25(3)23-16-20(18-9-7-6-8-10-18)15-21(24-23)19-11-12-22(26)17(2)14-19/h6-12,14-16,26H,4-5,13H2,1-3H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	790	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