Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Peroxisome proliferator-activated receptor alpha' and Ligand = 'BDBM50121420'   

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))	BDBM50121420 (CHEMBL330938 | Lithium; 2-(2,4-dichloro-benzoylami...) Show SMILES [O-]C(=O)c1cc(Oc2ncccc2[N+]([O-])=O)ccc1NC(=O)c1ccc(Cl)cc1Cl Show InChI InChI=1S/C19H11Cl2N3O6/c20-10-3-5-12(14(21)8-10)17(25)23-15-6-4-11(9-13(15)19(26)27)30-18-16(24(28)29)2-1-7-22-18/h1-9H,(H,23,25)(H,26,27)/p-1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	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 gamma				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))	BDBM50121420 (CHEMBL330938 | Lithium; 2-(2,4-dichloro-benzoylami...) Show SMILES [O-]C(=O)c1cc(Oc2ncccc2[N+]([O-])=O)ccc1NC(=O)c1ccc(Cl)cc1Cl Show InChI InChI=1S/C19H11Cl2N3O6/c20-10-3-5-12(14(21)8-10)17(25)23-15-6-4-11(9-13(15)19(26)27)30-18-16(24(28)29)2-1-7-22-18/h1-9H,(H,23,25)(H,26,27)/p-1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	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