null

SMILES: CC#CC(Cc1ccc(O)cc1)c1ccc(O)cc1

InChI Key: InChIKey=UUCSGILLVJJEAR-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50106637   

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))	BDBM50106637 (4-[2-(4-hydroxyphenyl)-3-pentynyl]phenol | CHEMBL1...) Show SMILES CC#CC(Cc1ccc(O)cc1)c1ccc(O)cc1 Show InChI InChI=1S/C17H16O2/c1-2-3-15(14-6-10-17(19)11-7-14)12-13-4-8-16(18)9-5-13/h4-11,15,18-19H,12H2,1H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	n/a	n/a	0.380	n/a	n/a	n/a	n/a
University of Illinois Curated by ChEMBL					Assay Description Transcriptional potency (EC50) at Human estrogen receptor alpha				J Med Chem 44: 4230-51 (2001) BindingDB Entry DOI: 10.7270/Q289155W
					More data for this Ligand-Target Pair
Estrogen receptor beta (Homo sapiens (Human))	BDBM50106637 (4-[2-(4-hydroxyphenyl)-3-pentynyl]phenol | CHEMBL1...) Show SMILES CC#CC(Cc1ccc(O)cc1)c1ccc(O)cc1 Show InChI InChI=1S/C17H16O2/c1-2-3-15(14-6-10-17(19)11-7-14)12-13-4-8-16(18)9-5-13/h4-11,15,18-19H,12H2,1H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	n/a	n/a	2.10	n/a	n/a	n/a	n/a
University of Illinois Curated by ChEMBL					Assay Description Transcriptional potency (EC50) at Human estrogen receptor Beta				J Med Chem 44: 4230-51 (2001) BindingDB Entry DOI: 10.7270/Q289155W
					More data for this Ligand-Target Pair