null

SMILES: CC(OC1=C(c2ccc(cc2)S(C)(=O)=O)C(C)(C)OC1=O)C1CC1

InChI Key: InChIKey=WTOORHANEMAYPO-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50080080   

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))	BDBM50080080 (3-(1-Cyclopropyl-ethoxy)-4-(4-methanesulfonyl-phen...) Show SMILES CC(OC1=C(c2ccc(cc2)S(C)(=O)=O)C(C)(C)OC1=O)C1CC1 |c:3| Show InChI InChI=1S/C18H22O5S/c1-11(12-5-6-12)22-16-15(18(2,3)23-17(16)19)13-7-9-14(10-8-13)24(4,20)21/h7-12H,5-6H2,1-4H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	3.60E+4	n/a	n/a	n/a	n/a	n/a	n/a
Merck Frosst Centre for Therapeutic Research Curated by ChEMBL					Assay Description Inhibitory activity against Prostaglandin G/H synthase 1 in human whole blood				Bioorg Med Chem Lett 9: 2207-12 (1999) BindingDB Entry DOI: 10.7270/Q2416W8T
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 2 (Homo sapiens (Human))	BDBM50080080 (3-(1-Cyclopropyl-ethoxy)-4-(4-methanesulfonyl-phen...) Show SMILES CC(OC1=C(c2ccc(cc2)S(C)(=O)=O)C(C)(C)OC1=O)C1CC1 |c:3| Show InChI InChI=1S/C18H22O5S/c1-11(12-5-6-12)22-16-15(18(2,3)23-17(16)19)13-7-9-14(10-8-13)24(4,20)21/h7-12H,5-6H2,1-4H3	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	80	n/a	n/a	n/a	n/a	n/a	n/a
Merck Frosst Centre for Therapeutic Research Curated by ChEMBL					Assay Description Inhibition of Prostaglandin G/H synthase 2 in human whole blood				Bioorg Med Chem Lett 9: 2207-12 (1999) BindingDB Entry DOI: 10.7270/Q2416W8T
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 1 (Homo sapiens (Human))	BDBM50080080 (3-(1-Cyclopropyl-ethoxy)-4-(4-methanesulfonyl-phen...) Show SMILES CC(OC1=C(c2ccc(cc2)S(C)(=O)=O)C(C)(C)OC1=O)C1CC1 |c:3| Show InChI InChI=1S/C18H22O5S/c1-11(12-5-6-12)22-16-15(18(2,3)23-17(16)19)13-7-9-14(10-8-13)24(4,20)21/h7-12H,5-6H2,1-4H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	6.50E+3	n/a	n/a	n/a	n/a	n/a	n/a
Merck Frosst Centre for Therapeutic Research Curated by ChEMBL					Assay Description Inhibitory activity against Human Cyclooxygenase-1 ( COX-1 ) in U937 Microsome COX-1 assay				Bioorg Med Chem Lett 9: 2207-12 (1999) BindingDB Entry DOI: 10.7270/Q2416W8T
					More data for this Ligand-Target Pair