Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Nuclear receptor ROR-gamma' and Ligand = 'BDBM338397'   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kJ/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))	BDBM338397 ((3S,6R)-2-[[2-fluoro-4-[(3R,4R)-3- fluoro-4-(1,2,4...) Show SMILES C[C@H]1CC[C@H](c2ccccc2)S(=O)(=O)N1Cc1ccc(cc1F)N1CC[C@H]([C@H](F)C1)n1cnnc1 |r| Show InChI InChI=1S/C25H29F2N5O2S/c1-18-7-10-25(19-5-3-2-4-6-19)35(33,34)32(18)14-20-8-9-21(13-22(20)26)30-12-11-24(23(27)15-30)31-16-28-29-17-31/h2-6,8-9,13,16-18,23-25H,7,10-12,14-15H2,1H3/t18-,23+,24+,25+/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	13.9	n/a	n/a	n/a	n/a	n/a	n/a
Genentech, Inc. US Patent					Assay Description Assays were carried out in 16-microL reaction volumes in black 384 Plus F Proxiplates (Perkin-Elmer 6008269). All assay components except test ligand...				US Patent US9751873 (2017) BindingDB Entry DOI: 10.7270/Q2BC41NZ
					More data for this Ligand-Target Pair
Nuclear receptor ROR-gamma (Homo sapiens (Human))	BDBM338397 ((3S,6R)-2-[[2-fluoro-4-[(3R,4R)-3- fluoro-4-(1,2,4...) Show SMILES C[C@H]1CC[C@H](c2ccccc2)S(=O)(=O)N1Cc1ccc(cc1F)N1CC[C@H]([C@H](F)C1)n1cnnc1 |r| Show InChI InChI=1S/C25H29F2N5O2S/c1-18-7-10-25(19-5-3-2-4-6-19)35(33,34)32(18)14-20-8-9-21(13-22(20)26)30-12-11-24(23(27)15-30)31-16-28-29-17-31/h2-6,8-9,13,16-18,23-25H,7,10-12,14-15H2,1H3/t18-,23+,24+,25+/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	14	n/a	n/a	n/a	n/a	n/a	n/a
Genentech, Inc. US Patent					Assay Description Assays were carried out in 16-microL reaction volumes in black 384 Plus F Proxiplates (Perkin-Elmer 6008269). All assay components except test ligand...				US Patent US9751873 (2017) BindingDB Entry DOI: 10.7270/Q2BC41NZ
					More data for this Ligand-Target Pair