null

SMILES: Cc1ccc(cc1)S(=O)(=O)N(CC(=O)NCc1ccc(F)cc1)c1cccc(c1)C(F)(F)F

InChI Key: InChIKey=UKEUPKBMEBZYEJ-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50164892   

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
Nuclear receptor ROR-gamma (Homo sapiens (Human))	BDBM50164892 (CHEMBL3799931) Show SMILES Cc1ccc(cc1)S(=O)(=O)N(CC(=O)NCc1ccc(F)cc1)c1cccc(c1)C(F)(F)F Show InChI InChI=1S/C23H20F4N2O3S/c1-16-5-11-21(12-6-16)33(31,32)29(20-4-2-3-18(13-20)23(25,26)27)15-22(30)28-14-17-7-9-19(24)10-8-17/h2-13H,14-15H2,1H3,(H,28,30)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	7.51E+3	n/a	n/a	n/a	n/a	n/a	n/a
Jilin University Curated by ChEMBL					Assay Description Inhibition of Gal4-RORgamma-LBD (180 to 507 residues) (unknown origin) expressed in HEK293T cells after 24 hrs by dual-luciferase reporter assay				Eur J Med Chem 116: 13-26 (2016) BindingDB Entry DOI: 10.7270/Q2TT4SVK
					More data for this Ligand-Target Pair
Nuclear receptor ROR-gamma (Homo sapiens (Human))	BDBM50164892 (CHEMBL3799931) Show SMILES Cc1ccc(cc1)S(=O)(=O)N(CC(=O)NCc1ccc(F)cc1)c1cccc(c1)C(F)(F)F Show InChI InChI=1S/C23H20F4N2O3S/c1-16-5-11-21(12-6-16)33(31,32)29(20-4-2-3-18(13-20)23(25,26)27)15-22(30)28-14-17-7-9-19(24)10-8-17/h2-13H,14-15H2,1H3,(H,28,30)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.31E+4	n/a	n/a	n/a	n/a	n/a	n/a
Jilin University Curated by ChEMBL					Assay Description Displacement of N-terminal biotinylated SRC1-4 coactivator peptide from N-terminal His6-fused human RORgamma-LBD (262 to 507 residues) expressed in E...				Eur J Med Chem 116: 13-26 (2016) BindingDB Entry DOI: 10.7270/Q2TT4SVK
					More data for this Ligand-Target Pair