null

SMILES: CC1=CC(C)(C)[C@@]2(O)CO[C@H]([C@@H]1C2)c1ccc(O)cc1Cl

InChI Key: InChIKey=MEHODSZURFPMSE-QJOPWCIASA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50161608   

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))	BDBM50161608 ((1R,4R,5R)-4-(2-Chloro-4-hydroxy-phenyl)-6,8,8-tri...) Show SMILES CC1=CC(C)(C)[C@@]2(O)CO[C@H]([C@@H]1C2)c1ccc(O)cc1Cl |t:1| Show InChI InChI=1S/C17H21ClO3/c1-10-7-16(2,3)17(20)8-13(10)15(21-9-17)12-5-4-11(19)6-14(12)18/h4-7,13,15,19-20H,8-9H2,1-3H3/t13?,15-,17-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	25	n/a	n/a	n/a	n/a
Ligand Pharmaceuticals Curated by ChEMBL					Assay Description In vitro agonist activity for estrogen receptor beta expressed in COS-1 cells				Bioorg Med Chem Lett 15: 1463-6 (2005) Article DOI: 10.1016/j.bmcl.2004.12.077 BindingDB Entry DOI: 10.7270/Q25H7FR7
					More data for this Ligand-Target Pair
Estrogen receptor (Homo sapiens (Human))	BDBM50161608 ((1R,4R,5R)-4-(2-Chloro-4-hydroxy-phenyl)-6,8,8-tri...) Show SMILES CC1=CC(C)(C)[C@@]2(O)CO[C@H]([C@@H]1C2)c1ccc(O)cc1Cl |t:1| Show InChI InChI=1S/C17H21ClO3/c1-10-7-16(2,3)17(20)8-13(10)15(21-9-17)12-5-4-11(19)6-14(12)18/h4-7,13,15,19-20H,8-9H2,1-3H3/t13?,15-,17-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	21	n/a	n/a	n/a	n/a
Ligand Pharmaceuticals Curated by ChEMBL					Assay Description In vitro agonist activity for estrogen receptor alpha expressed in COS-1 cells				Bioorg Med Chem Lett 15: 1463-6 (2005) Article DOI: 10.1016/j.bmcl.2004.12.077 BindingDB Entry DOI: 10.7270/Q25H7FR7
					More data for this Ligand-Target Pair