null

SMILES: NS(=O)(=O)c1ccc(cc1)-c1coc(=O)n1-c1ccc(Cl)cc1

InChI Key: InChIKey=LQPFLKVMDLZLBB-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50084356   

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
Prostaglandin G/H synthase 1 (Homo sapiens (Human))	BDBM50084356 (4-[3-(4-Chloro-phenyl)-2-oxo-2,3-dihydro-oxazol-4-...) Show SMILES NS(=O)(=O)c1ccc(cc1)-c1coc(=O)n1-c1ccc(Cl)cc1 Show InChI InChI=1S/C15H11ClN2O4S/c16-11-3-5-12(6-4-11)18-14(9-22-15(18)19)10-1-7-13(8-2-10)23(17,20)21/h1-9H,(H2,17,20,21)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	7.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Rhône-Poulenc Rorer Curated by ChEMBL					Assay Description Inhibitory activity against prostaglandin G/H synthase 1				J Med Chem 43: 214-23 (2000) BindingDB Entry DOI: 10.7270/Q2DV1KK0
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 2 (Homo sapiens (Human))	BDBM50084356 (4-[3-(4-Chloro-phenyl)-2-oxo-2,3-dihydro-oxazol-4-...) Show SMILES NS(=O)(=O)c1ccc(cc1)-c1coc(=O)n1-c1ccc(Cl)cc1 Show InChI InChI=1S/C15H11ClN2O4S/c16-11-3-5-12(6-4-11)18-14(9-22-15(18)19)10-1-7-13(8-2-10)23(17,20)21/h1-9H,(H2,17,20,21)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	1.20E+3	n/a	n/a	n/a	n/a	n/a	n/a
Jadavpur University Curated by ChEMBL					Assay Description Binding affinity towards Prostaglandin G/H synthase 2				Bioorg Med Chem Lett 13: 3753-7 (2003) BindingDB Entry DOI: 10.7270/Q2JM2BS0
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 1 (Homo sapiens (Human))	BDBM50084356 (4-[3-(4-Chloro-phenyl)-2-oxo-2,3-dihydro-oxazol-4-...) Show SMILES NS(=O)(=O)c1ccc(cc1)-c1coc(=O)n1-c1ccc(Cl)cc1 Show InChI InChI=1S/C15H11ClN2O4S/c16-11-3-5-12(6-4-11)18-14(9-22-15(18)19)10-1-7-13(8-2-10)23(17,20)21/h1-9H,(H2,17,20,21)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	7.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Jadavpur University Curated by ChEMBL					Assay Description Binding affinity towards Prostaglandin G/H synthase 1				Bioorg Med Chem Lett 13: 3753-7 (2003) BindingDB Entry DOI: 10.7270/Q2JM2BS0
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 2 (Homo sapiens (Human))	BDBM50084356 (4-[3-(4-Chloro-phenyl)-2-oxo-2,3-dihydro-oxazol-4-...) Show SMILES NS(=O)(=O)c1ccc(cc1)-c1coc(=O)n1-c1ccc(Cl)cc1 Show InChI InChI=1S/C15H11ClN2O4S/c16-11-3-5-12(6-4-11)18-14(9-22-15(18)19)10-1-7-13(8-2-10)23(17,20)21/h1-9H,(H2,17,20,21)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	1.20E+3	n/a	n/a	n/a	n/a	n/a	n/a
Rhône-Poulenc Rorer Curated by ChEMBL					Assay Description Inhibitory activity against prostaglandin G/H synthase 2				J Med Chem 43: 214-23 (2000) BindingDB Entry DOI: 10.7270/Q2DV1KK0
					More data for this Ligand-Target Pair