Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Peroxisome proliferator-activated receptor alpha' and Ligand = 'BDBM50121418'   

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
Peroxisome proliferator-activated receptor alpha (Homo sapiens (Human))	BDBM50121418 (CHEMBL119078 | Lithium; 2-(2,4-dichloro-benzoylami...) Show SMILES [O-]C(=O)c1cc(ccc1NC(=O)c1ccc(Cl)cc1Cl)-c1cccc2cccnc12 Show InChI InChI=1S/C23H14Cl2N2O3/c24-15-7-8-17(19(25)12-15)22(28)27-20-9-6-14(11-18(20)23(29)30)16-5-1-3-13-4-2-10-26-21(13)16/h1-12H,(H,27,28)(H,29,30)/p-1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Biovitrum AB Curated by ChEMBL					Assay Description Transactivation potency was measured by luciferase activity in Caco- 2/TC7 cells transiently co-transfected for the fusion-protein Gal4-PPAR alpha				Bioorg Med Chem Lett 12: 3565-7 (2002) BindingDB Entry DOI: 10.7270/Q2Q23ZK5
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor alpha (Homo sapiens (Human))	BDBM50121418 (CHEMBL119078 | Lithium; 2-(2,4-dichloro-benzoylami...) Show SMILES [O-]C(=O)c1cc(ccc1NC(=O)c1ccc(Cl)cc1Cl)-c1cccc2cccnc12 Show InChI InChI=1S/C23H14Cl2N2O3/c24-15-7-8-17(19(25)12-15)22(28)27-20-9-6-14(11-18(20)23(29)30)16-5-1-3-13-4-2-10-26-21(13)16/h1-12H,(H,27,28)(H,29,30)/p-1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a
Biovitrum AB Curated by ChEMBL					Assay Description Transactivation potency was measured by luciferase activity in Caco- 2/TC7 cells transiently co-transfected for the fusion-protein Gal4-PPAR alpha				Bioorg Med Chem Lett 12: 3565-7 (2002) BindingDB Entry DOI: 10.7270/Q2Q23ZK5
					More data for this Ligand-Target Pair