null

SMILES: [O-]C(=O)c1cc(OCCc2cccs2)ccc1NC(=O)c1ccc(Cl)cc1Cl

InChI Key: InChIKey=VBJDTFMKZNAHSC-UHFFFAOYSA-M

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50121423   

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))	BDBM50121423 (CHEMBL119278 | Lithium; 2-(2,4-dichloro-benzoylami...) Show SMILES [O-]C(=O)c1cc(OCCc2cccs2)ccc1NC(=O)c1ccc(Cl)cc1Cl Show InChI InChI=1S/C20H15Cl2NO4S/c21-12-3-5-15(17(22)10-12)19(24)23-18-6-4-13(11-16(18)20(25)26)27-8-7-14-2-1-9-28-14/h1-6,9-11H,7-8H2,(H,23,24)(H,25,26)/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	1.00E+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))	BDBM50121423 (CHEMBL119278 | Lithium; 2-(2,4-dichloro-benzoylami...) Show SMILES [O-]C(=O)c1cc(OCCc2cccs2)ccc1NC(=O)c1ccc(Cl)cc1Cl Show InChI InChI=1S/C20H15Cl2NO4S/c21-12-3-5-15(17(22)10-12)19(24)23-18-6-4-13(11-16(18)20(25)26)27-8-7-14-2-1-9-28-14/h1-6,9-11H,7-8H2,(H,23,24)(H,25,26)/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 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))	BDBM50121423 (CHEMBL119278 | Lithium; 2-(2,4-dichloro-benzoylami...) Show SMILES [O-]C(=O)c1cc(OCCc2cccs2)ccc1NC(=O)c1ccc(Cl)cc1Cl Show InChI InChI=1S/C20H15Cl2NO4S/c21-12-3-5-15(17(22)10-12)19(24)23-18-6-4-13(11-16(18)20(25)26)27-8-7-14-2-1-9-28-14/h1-6,9-11H,7-8H2,(H,23,24)(H,25,26)/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	700	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))	BDBM50121423 (CHEMBL119278 | Lithium; 2-(2,4-dichloro-benzoylami...) Show SMILES [O-]C(=O)c1cc(OCCc2cccs2)ccc1NC(=O)c1ccc(Cl)cc1Cl Show InChI InChI=1S/C20H15Cl2NO4S/c21-12-3-5-15(17(22)10-12)19(24)23-18-6-4-13(11-16(18)20(25)26)27-8-7-14-2-1-9-28-14/h1-6,9-11H,7-8H2,(H,23,24)(H,25,26)/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