null

SMILES: CN(Cc1ccc(Br)s1)C(=O)c1cc2ccc(F)cc2[nH]1

InChI Key: InChIKey=OKKABFIPSDJEGN-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50051053   

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
Androgen receptor (Homo sapiens (Human))	BDBM50051053 (CHEMBL3318059) Show SMILES CN(Cc1ccc(Br)s1)C(=O)c1cc2ccc(F)cc2[nH]1 Show InChI InChI=1S/C15H12BrFN2OS/c1-19(8-11-4-5-14(16)21-11)15(20)13-6-9-2-3-10(17)7-12(9)18-13/h2-7,18H,8H2,1H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.53E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of British Columbia Curated by ChEMBL					Assay Description Inhibition of androgen receptor binding function 3 in eGFP-expressing human LNCAP cells containing androgen-responsive probasin-derived promoter asse...				J Med Chem 57: 6867-72 (2014) Article DOI: 10.1021/jm500684r BindingDB Entry DOI: 10.7270/Q29S1SNR
					More data for this Ligand-Target Pair
Androgen receptor (Homo sapiens (Human))	BDBM50051053 (CHEMBL3318059) Show SMILES CN(Cc1ccc(Br)s1)C(=O)c1cc2ccc(F)cc2[nH]1 Show InChI InChI=1S/C15H12BrFN2OS/c1-19(8-11-4-5-14(16)21-11)15(20)13-6-9-2-3-10(17)7-12(9)18-13/h2-7,18H,8H2,1H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.06E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of British Columbia Curated by ChEMBL					Assay Description Inhibition of androgen receptor binding function 3 in human LNCAP cells containing androgen-responsive probasin-derived promoter assessed as reductio...				J Med Chem 57: 6867-72 (2014) Article DOI: 10.1021/jm500684r BindingDB Entry DOI: 10.7270/Q29S1SNR
					More data for this Ligand-Target Pair