null

SMILES: Cc1nocc1-c1nc2ccccc2n1-c1ccc(O)cc1

InChI Key: InChIKey=VVQKKJATDFFYEJ-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50175417   

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))	BDBM50175417 (4-(2-(3-methylisoxazol-4-yl)-1H-benzo[d]imidazol-1...) Show SMILES Cc1nocc1-c1nc2ccccc2n1-c1ccc(O)cc1 Show InChI InChI=1S/C17H13N3O2/c1-11-14(10-22-19-11)17-18-15-4-2-3-5-16(15)20(17)12-6-8-13(21)9-7-12/h2-10,21H,1H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.16E+3	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer Global Research and Development Curated by ChEMBL					Assay Description Displacement of [3H]17beta-estradiol from recombinant human ERalpha expressed in 293T cells				Bioorg Med Chem Lett 15: 5562-6 (2005) Article DOI: 10.1016/j.bmcl.2005.08.010 BindingDB Entry DOI: 10.7270/Q2N879CK
					More data for this Ligand-Target Pair
Estrogen receptor beta (Homo sapiens (Human))	BDBM50175417 (4-(2-(3-methylisoxazol-4-yl)-1H-benzo[d]imidazol-1...) Show SMILES Cc1nocc1-c1nc2ccccc2n1-c1ccc(O)cc1 Show InChI InChI=1S/C17H13N3O2/c1-11-14(10-22-19-11)17-18-15-4-2-3-5-16(15)20(17)12-6-8-13(21)9-7-12/h2-10,21H,1H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	14.3	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer Global Research and Development Curated by ChEMBL					Assay Description Displacement of [3H]17beta-estradiol from recombinant human ERbeta expressed in 293T cells				Bioorg Med Chem Lett 15: 5562-6 (2005) Article DOI: 10.1016/j.bmcl.2005.08.010 BindingDB Entry DOI: 10.7270/Q2N879CK
					More data for this Ligand-Target Pair