null

SMILES: CCC1=C(Cc2cc(O)ccc12)c1ccc(O)cc1

InChI Key: InChIKey=NDOHHPHBVZUFJE-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50173667   

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))	BDBM50173667 (1-Ethyl-2-(4-hydroxy-phenyl)-3H-inden-5-ol | CHEMB...) Show SMILES CCC1=C(Cc2cc(O)ccc12)c1ccc(O)cc1 |t:2| Show InChI InChI=1S/C17H16O2/c1-2-15-16-8-7-14(19)9-12(16)10-17(15)11-3-5-13(18)6-4-11/h3-9,18-19H,2,10H2,1H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	0.310	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
Estrogen receptor beta (Homo sapiens (Human))	BDBM50173667 (1-Ethyl-2-(4-hydroxy-phenyl)-3H-inden-5-ol | CHEMB...) Show SMILES CCC1=C(Cc2cc(O)ccc12)c1ccc(O)cc1 |t:2| Show InChI InChI=1S/C17H16O2/c1-2-15-16-8-7-14(19)9-12(16)10-17(15)11-3-5-13(18)6-4-11/h3-9,18-19H,2,10H2,1H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	0.300	n/a	n/a	n/a	n/a
University of California Curated by ChEMBL					Assay Description Transcriptional activation of estrogen receptor beta in U2OS cell using estrogen-regulated luciferase reporter gene plasmid upon incubation for 20-30...				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