null

SMILES: [O-]C(=O)c1cc(ccc1NC(=O)c1ccc(Cl)cc1Cl)-c1ccco1

InChI Key: InChIKey=IVQFOWVLYRHJKW-UHFFFAOYSA-M

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50121415   

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
Peroxisome proliferator-activated receptor gamma (Homo sapiens (Human))	BDBM50121415 (CHEMBL119030 | Lithium; 2-(2,4-dichloro-benzoylami...) Show SMILES [O-]C(=O)c1cc(ccc1NC(=O)c1ccc(Cl)cc1Cl)-c1ccco1 Show InChI InChI=1S/C18H11Cl2NO4/c19-11-4-5-12(14(20)9-11)17(22)21-15-6-3-10(8-13(15)18(23)24)16-2-1-7-25-16/h1-9H,(H,21,22)(H,23,24)/p-1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	500	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Biovitrum AB Curated by ChEMBL					Assay Description Ligand binding affinity was determined by displacement of a tritiated tracer by the unlabeled compound to a GST-PPAR fusion protein for Peroxisome pr...				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))	BDBM50121415 (CHEMBL119030 | Lithium; 2-(2,4-dichloro-benzoylami...) Show SMILES [O-]C(=O)c1cc(ccc1NC(=O)c1ccc(Cl)cc1Cl)-c1ccco1 Show InChI InChI=1S/C18H11Cl2NO4/c19-11-4-5-12(14(20)9-11)17(22)21-15-6-3-10(8-13(15)18(23)24)16-2-1-7-25-16/h1-9H,(H,21,22)(H,23,24)/p-1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	2.20E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Biovitrum AB Curated by ChEMBL					Assay Description Ligand binding affinity was determined by displacement of a tritiated tracer by the unlabeled compound to a GST-PPAR fusion protein for Peroxisome pr...				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 gamma (Homo sapiens (Human))	BDBM50121415 (CHEMBL119030 | Lithium; 2-(2,4-dichloro-benzoylami...) Show SMILES [O-]C(=O)c1cc(ccc1NC(=O)c1ccc(Cl)cc1Cl)-c1ccco1 Show InChI InChI=1S/C18H11Cl2NO4/c19-11-4-5-12(14(20)9-11)17(22)21-15-6-3-10(8-13(15)18(23)24)16-2-1-7-25-16/h1-9H,(H,21,22)(H,23,24)/p-1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	n/a	n/a	1.00E+3	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))	BDBM50121415 (CHEMBL119030 | Lithium; 2-(2,4-dichloro-benzoylami...) Show SMILES [O-]C(=O)c1cc(ccc1NC(=O)c1ccc(Cl)cc1Cl)-c1ccco1 Show InChI InChI=1S/C18H11Cl2NO4/c19-11-4-5-12(14(20)9-11)17(22)21-15-6-3-10(8-13(15)18(23)24)16-2-1-7-25-16/h1-9H,(H,21,22)(H,23,24)/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+4	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