null

SMILES: CN(CCc1ccccc1)c1cc(cc(n1)-c1ccc(O)c(C)c1)-c1ccccc1

InChI Key: InChIKey=CNZVGKSWGGJIMU-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50102190   

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))	BDBM50102190 (2-Methyl-4-[6-(methyl-phenethyl-amino)-4-phenyl-py...) Show SMILES CN(CCc1ccccc1)c1cc(cc(n1)-c1ccc(O)c(C)c1)-c1ccccc1 Show InChI InChI=1S/C27H26N2O/c1-20-17-23(13-14-26(20)30)25-18-24(22-11-7-4-8-12-22)19-27(28-25)29(2)16-15-21-9-5-3-6-10-21/h3-14,17-19,30H,15-16H2,1-2H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	160	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))	BDBM50102190 (2-Methyl-4-[6-(methyl-phenethyl-amino)-4-phenyl-py...) Show SMILES CN(CCc1ccccc1)c1cc(cc(n1)-c1ccc(O)c(C)c1)-c1ccccc1 Show InChI InChI=1S/C27H26N2O/c1-20-17-23(13-14-26(20)30)25-18-24(22-11-7-4-8-12-22)19-27(28-25)29(2)16-15-21-9-5-3-6-10-21/h3-14,17-19,30H,15-16H2,1-2H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	680	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