BDBM50051050 CHEMBL3318062

SMILES: CC(C)N(Cc1ccc(C)o1)C(=O)c1cc2ccc(C)cc2[nH]1

InChI Key: InChIKey=DJXCHFZTNXMPTB-UHFFFAOYSA-N

Data: 2 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 2 hits for monomerid = 50051050   

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))	BDBM50051050 (CHEMBL3318062) Show SMILES CC(C)N(Cc1ccc(C)o1)C(=O)c1cc2ccc(C)cc2[nH]1 Show InChI InChI=1S/C19H22N2O2/c1-12(2)21(11-16-8-6-14(4)23-16)19(22)18-10-15-7-5-13(3)9-17(15)20-18/h5-10,12,20H,11H2,1-4H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.89E+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))	BDBM50051050 (CHEMBL3318062) Show SMILES CC(C)N(Cc1ccc(C)o1)C(=O)c1cc2ccc(C)cc2[nH]1 Show InChI InChI=1S/C19H22N2O2/c1-12(2)21(11-16-8-6-14(4)23-16)19(22)18-10-15-7-5-13(3)9-17(15)20-18/h5-10,12,20H,11H2,1-4H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.65E+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