null

SMILES: OC(=O)c1cccc(c1)-c1ccc(NC(=O)c2ccc(Cl)cc2Cl)c(c1)C([O-])=O

InChI Key: InChIKey=PKHBDCMHNSWKKS-UHFFFAOYSA-M

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50121416   

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))	BDBM50121416 (CHEMBL325172 | Lithium; 3'-carboxy-4-(2,4-dichloro...) Show SMILES OC(=O)c1cccc(c1)-c1ccc(NC(=O)c2ccc(Cl)cc2Cl)c(c1)C([O-])=O Show InChI InChI=1S/C21H13Cl2NO5/c22-14-5-6-15(17(23)10-14)19(25)24-18-7-4-12(9-16(18)21(28)29)11-2-1-3-13(8-11)20(26)27/h1-10H,(H,24,25)(H,26,27)(H,28,29)/p-1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	1.40E+3	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))	BDBM50121416 (CHEMBL325172 | Lithium; 3'-carboxy-4-(2,4-dichloro...) Show SMILES OC(=O)c1cccc(c1)-c1ccc(NC(=O)c2ccc(Cl)cc2Cl)c(c1)C([O-])=O Show InChI InChI=1S/C21H13Cl2NO5/c22-14-5-6-15(17(23)10-14)19(25)24-18-7-4-12(9-16(18)21(28)29)11-2-1-3-13(8-11)20(26)27/h1-10H,(H,24,25)(H,26,27)(H,28,29)/p-1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	6.70E+4	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 gamma (Homo sapiens (Human))	BDBM50121416 (CHEMBL325172 | Lithium; 3'-carboxy-4-(2,4-dichloro...) Show SMILES OC(=O)c1cccc(c1)-c1ccc(NC(=O)c2ccc(Cl)cc2Cl)c(c1)C([O-])=O Show InChI InChI=1S/C21H13Cl2NO5/c22-14-5-6-15(17(23)10-14)19(25)24-18-7-4-12(9-16(18)21(28)29)11-2-1-3-13(8-11)20(26)27/h1-10H,(H,24,25)(H,26,27)(H,28,29)/p-1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank 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 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))	BDBM50121416 (CHEMBL325172 | Lithium; 3'-carboxy-4-(2,4-dichloro...) Show SMILES OC(=O)c1cccc(c1)-c1ccc(NC(=O)c2ccc(Cl)cc2Cl)c(c1)C([O-])=O Show InChI InChI=1S/C21H13Cl2NO5/c22-14-5-6-15(17(23)10-14)19(25)24-18-7-4-12(9-16(18)21(28)29)11-2-1-3-13(8-11)20(26)27/h1-10H,(H,24,25)(H,26,27)(H,28,29)/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