Compile Data Set for Download or QSAR

Found 2 hits of ic50 for monomerid = 50174923   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kJ/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Estrogen receptor (Homo sapiens (Human))	BDBM50174923 ((5R,6S)-6-phenyl-5-(4-((S)-2-(pyrrolidin-1-yl)prop...) Show SMILES C[C@@H](COc1ccc(cc1)[C@H]1[C@H](CCc2cc(O)ccc12)c1ccccc1)N1CCCC1 Show InChI InChI=1S/C29H33NO2/c1-21(30-17-5-6-18-30)20-32-26-13-9-23(10-14-26)29-27(22-7-3-2-4-8-22)15-11-24-19-25(31)12-16-28(24)29/h2-4,7-10,12-14,16,19,21,27,29,31H,5-6,11,15,17-18,20H2,1H3/t21-,27+,29-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	0.600	n/a	n/a	n/a	n/a	n/a	n/a
Merck Research Laboratories Curated by ChEMBL					Assay Description Inhibition of binding to recombinant human ERalpha by scintillation proximity assay				Bioorg Med Chem Lett 15: 5124-8 (2005) Article DOI: 10.1016/j.bmcl.2005.08.084 BindingDB Entry DOI: 10.7270/Q2BZ65MS
					More data for this Ligand-Target Pair
Estrogen receptor beta (Homo sapiens (Human))	BDBM50174923 ((5R,6S)-6-phenyl-5-(4-((S)-2-(pyrrolidin-1-yl)prop...) Show SMILES C[C@@H](COc1ccc(cc1)[C@H]1[C@H](CCc2cc(O)ccc12)c1ccccc1)N1CCCC1 Show InChI InChI=1S/C29H33NO2/c1-21(30-17-5-6-18-30)20-32-26-13-9-23(10-14-26)29-27(22-7-3-2-4-8-22)15-11-24-19-25(31)12-16-28(24)29/h2-4,7-10,12-14,16,19,21,27,29,31H,5-6,11,15,17-18,20H2,1H3/t21-,27+,29-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	0.900	n/a	n/a	n/a	n/a	n/a	n/a
Merck Research Laboratories Curated by ChEMBL					Assay Description Inhibition of binding to recombinant human ERbeta by scintillation proximity assay				Bioorg Med Chem Lett 15: 5124-8 (2005) Article DOI: 10.1016/j.bmcl.2005.08.084 BindingDB Entry DOI: 10.7270/Q2BZ65MS
					More data for this Ligand-Target Pair