null

SMILES: C[C@H]1CC[C@@H]2[C@H](C1)c1cc3c(cc(=O)n(C)c3cc1N2C)C(F)(F)F

InChI Key: InChIKey=YQTCSWKPQXVKOV-FIXISWKDSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50069061   

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))	BDBM50069061 ((5bR,7S,9aR)-1,7,10-Trimethyl-4-trifluoromethyl-1,...) Show SMILES C[C@H]1CC[C@@H]2[C@H](C1)c1cc3c(cc(=O)n(C)c3cc1N2C)C(F)(F)F Show InChI InChI=1S/C19H21F3N2O/c1-10-4-5-15-11(6-10)12-7-13-14(19(20,21)22)8-18(25)24(3)17(13)9-16(12)23(15)2/h7-11,15H,4-6H2,1-3H3/t10-,11+,15+/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	78	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Ligand Pharmaceuticals Curated by ChEMBL					Assay Description Binding affinity against Androgen receptor transfected into COS cells				Bioorg Med Chem Lett 8: 745-50 (1999) BindingDB Entry DOI: 10.7270/Q2XS5THG
					More data for this Ligand-Target Pair
Androgen receptor (Homo sapiens (Human))	BDBM50069061 ((5bR,7S,9aR)-1,7,10-Trimethyl-4-trifluoromethyl-1,...) Show SMILES C[C@H]1CC[C@@H]2[C@H](C1)c1cc3c(cc(=O)n(C)c3cc1N2C)C(F)(F)F Show InChI InChI=1S/C19H21F3N2O/c1-10-4-5-15-11(6-10)12-7-13-14(19(20,21)22)8-18(25)24(3)17(13)9-16(12)23(15)2/h7-11,15H,4-6H2,1-3H3/t10-,11+,15+/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	54	n/a	n/a	n/a	n/a	n/a	n/a
Ligand Pharmaceuticals Curated by ChEMBL					Assay Description Antagonistic activity (IC50) against human androgen receptor (hAR) in cotransfected CV-1 cell				Bioorg Med Chem Lett 8: 745-50 (1999) BindingDB Entry DOI: 10.7270/Q2XS5THG
					More data for this Ligand-Target Pair