null

SMILES: Cc1ccc(cc1)C1=C(Cc2cc(O)ccc12)c1ccc(O)cc1

InChI Key: InChIKey=YIFNILRPNDYIBP-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50173668   

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 beta (Homo sapiens (Human))	BDBM50173668 (2-(4-Hydroxy-phenyl)-1-p-tolyl-3H-inden-5-ol | CHE...) Show SMILES Cc1ccc(cc1)C1=C(Cc2cc(O)ccc12)c1ccc(O)cc1 |t:8| Show InChI InChI=1S/C22H18O2/c1-14-2-4-16(5-3-14)22-20-11-10-19(24)12-17(20)13-21(22)15-6-8-18(23)9-7-15/h2-12,23-24H,13H2,1H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.30	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of California Curated by ChEMBL					Assay Description Antagonistic activity against estrogen receptor beta in presence of 0.1 nM estradiol				J Med Chem 48: 5989-6003 (2005) Article DOI: 10.1021/jm050226i BindingDB Entry DOI: 10.7270/Q2B857P7
					More data for this Ligand-Target Pair
Estrogen receptor (Homo sapiens (Human))	BDBM50173668 (2-(4-Hydroxy-phenyl)-1-p-tolyl-3H-inden-5-ol | CHE...) Show SMILES Cc1ccc(cc1)C1=C(Cc2cc(O)ccc12)c1ccc(O)cc1 |t:8| Show InChI InChI=1S/C22H18O2/c1-14-2-4-16(5-3-14)22-20-11-10-19(24)12-17(20)13-21(22)15-6-8-18(23)9-7-15/h2-12,23-24H,13H2,1H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	17	n/a	n/a	n/a	n/a
University of California Curated by ChEMBL					Assay Description Transcriptional activation of estrogen receptor alpha in U2OS cell using estrogen-regulated luciferase reporter gene plasmid upon incubation for 20-3...				J Med Chem 48: 5989-6003 (2005) Article DOI: 10.1021/jm050226i BindingDB Entry DOI: 10.7270/Q2B857P7
					More data for this Ligand-Target Pair