null

SMILES: CSCCOc1ccc(NC(=O)c2ccc(Cl)cc2Cl)c(c1)C([O-])=O

InChI Key: InChIKey=NUFOUZIOJRXDFK-UHFFFAOYSA-M

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50121417   

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))	BDBM50121417 (CHEMBL119646 | Lithium; 2-(2,4-dichloro-benzoylami...) Show SMILES CSCCOc1ccc(NC(=O)c2ccc(Cl)cc2Cl)c(c1)C([O-])=O Show InChI InChI=1S/C17H15Cl2NO4S/c1-25-7-6-24-11-3-5-15(13(9-11)17(22)23)20-16(21)12-4-2-10(18)8-14(12)19/h2-5,8-9H,6-7H2,1H3,(H,20,21)(H,22,23)/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	1.60E+3	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))	BDBM50121417 (CHEMBL119646 | Lithium; 2-(2,4-dichloro-benzoylami...) Show SMILES CSCCOc1ccc(NC(=O)c2ccc(Cl)cc2Cl)c(c1)C([O-])=O Show InChI InChI=1S/C17H15Cl2NO4S/c1-25-7-6-24-11-3-5-15(13(9-11)17(22)23)20-16(21)12-4-2-10(18)8-14(12)19/h2-5,8-9H,6-7H2,1H3,(H,20,21)(H,22,23)/p-1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	1.90E+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))	BDBM50121417 (CHEMBL119646 | Lithium; 2-(2,4-dichloro-benzoylami...) Show SMILES CSCCOc1ccc(NC(=O)c2ccc(Cl)cc2Cl)c(c1)C([O-])=O Show InChI InChI=1S/C17H15Cl2NO4S/c1-25-7-6-24-11-3-5-15(13(9-11)17(22)23)20-16(21)12-4-2-10(18)8-14(12)19/h2-5,8-9H,6-7H2,1H3,(H,20,21)(H,22,23)/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	600	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))	BDBM50121417 (CHEMBL119646 | Lithium; 2-(2,4-dichloro-benzoylami...) Show SMILES CSCCOc1ccc(NC(=O)c2ccc(Cl)cc2Cl)c(c1)C([O-])=O Show InChI InChI=1S/C17H15Cl2NO4S/c1-25-7-6-24-11-3-5-15(13(9-11)17(22)23)20-16(21)12-4-2-10(18)8-14(12)19/h2-5,8-9H,6-7H2,1H3,(H,20,21)(H,22,23)/p-1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	n/a	n/a	2.50E+3	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