BDBM50425755 CHEMBL2316551

SMILES: CC(C)(C)c1cccc(OCCSc2nc3ccccc3n2CC(O)=O)c1

InChI Key: InChIKey=BSYGSNLDVGMRCD-UHFFFAOYSA-N

Data: 1 IC50

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50425755   

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))	BDBM50425755 (CHEMBL2316551) Show SMILES CC(C)(C)c1cccc(OCCSc2nc3ccccc3n2CC(O)=O)c1 Show InChI InChI=1S/C21H24N2O3S/c1-21(2,3)15-7-6-8-16(13-15)26-11-12-27-20-22-17-9-4-5-10-18(17)23(20)14-19(24)25/h4-10,13H,11-12,14H2,1-3H3,(H,24,25)	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	>2.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
University of British Columbia Curated by ChEMBL					Assay Description Inhibition of BF3 site of androgen receptor in human LNCAP cells expressing ARR2PB after 3 days by eGFP transcriptional assay				J Med Chem 56: 1136-48 (2013) Article DOI: 10.1021/jm3015712 BindingDB Entry DOI: 10.7270/Q2ZW1N7N
					More data for this Ligand-Target Pair