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SMILES: CN(Cc1ccccc1)c1cc(cc(n1)-c1ccc(O)c(C)c1)-c1ccccc1

InChI Key: InChIKey=MOJUIGSJBXXTNA-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50102203   

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))	BDBM50102203 (4-[6-(Benzyl-methyl-amino)-4-phenyl-pyridin-2-yl]-...) Show SMILES CN(Cc1ccccc1)c1cc(cc(n1)-c1ccc(O)c(C)c1)-c1ccccc1 Show InChI InChI=1S/C26H24N2O/c1-19-15-22(13-14-25(19)29)24-16-23(21-11-7-4-8-12-21)17-26(27-24)28(2)18-20-9-5-3-6-10-20/h3-17,29H,18H2,1-2H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	380	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))	BDBM50102203 (4-[6-(Benzyl-methyl-amino)-4-phenyl-pyridin-2-yl]-...) Show SMILES CN(Cc1ccccc1)c1cc(cc(n1)-c1ccc(O)c(C)c1)-c1ccccc1 Show InChI InChI=1S/C26H24N2O/c1-19-15-22(13-14-25(19)29)24-16-23(21-11-7-4-8-12-21)17-26(27-24)28(2)18-20-9-5-3-6-10-20/h3-17,29H,18H2,1-2H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	1.12E+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