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SMILES: Cc1cc(ccc1O)-c1cc(cc(n1)N(CCc1ccccc1)Cc1ccccc1)-c1ccccc1

InChI Key: InChIKey=NNSHOBXASKSVQK-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50102205   

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))	BDBM50102205 (4-[6-(Benzyl-phenethyl-amino)-4-phenyl-pyridin-2-y...) Show SMILES Cc1cc(ccc1O)-c1cc(cc(n1)N(CCc1ccccc1)Cc1ccccc1)-c1ccccc1 Show InChI InChI=1S/C33H30N2O/c1-25-21-29(17-18-32(25)36)31-22-30(28-15-9-4-10-16-28)23-33(34-31)35(24-27-13-7-3-8-14-27)20-19-26-11-5-2-6-12-26/h2-18,21-23,36H,19-20,24H2,1H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	130	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))	BDBM50102205 (4-[6-(Benzyl-phenethyl-amino)-4-phenyl-pyridin-2-y...) Show SMILES Cc1cc(ccc1O)-c1cc(cc(n1)N(CCc1ccccc1)Cc1ccccc1)-c1ccccc1 Show InChI InChI=1S/C33H30N2O/c1-25-21-29(17-18-32(25)36)31-22-30(28-15-9-4-10-16-28)23-33(34-31)35(24-27-13-7-3-8-14-27)20-19-26-11-5-2-6-12-26/h2-18,21-23,36H,19-20,24H2,1H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	250	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