null

SMILES: CC(C(O)=O)c1ccc(Cc2ccc(F)cc2)c2ccccc12

InChI Key: InChIKey=KDXOWJPNWSWNAA-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50105284   

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 2 (RAT)	BDBM50105284 (2-[4-(4-Fluoro-benzyl)-naphthalen-1-yl]-propionic ...) Show SMILES CC(C(O)=O)c1ccc(Cc2ccc(F)cc2)c2ccccc12 Show InChI InChI=1S/C20H17FO2/c1-13(20(22)23)17-11-8-15(18-4-2-3-5-19(17)18)12-14-6-9-16(21)10-7-14/h2-11,13H,12H2,1H3,(H,22,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	3.50E+3	n/a	n/a	n/a	n/a	n/a	n/a
Rhône-Poulenc Rorer Curated by ChEMBL					Assay Description In vitro inhibitory concentration against rat Prostaglandin G/H synthase 2				Bioorg Med Chem Lett 11: 2687-90 (2001) BindingDB Entry DOI: 10.7270/Q2BC3XV1
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 1 (RAT)	BDBM50105284 (2-[4-(4-Fluoro-benzyl)-naphthalen-1-yl]-propionic ...) Show SMILES CC(C(O)=O)c1ccc(Cc2ccc(F)cc2)c2ccccc12 Show InChI InChI=1S/C20H17FO2/c1-13(20(22)23)17-11-8-15(18-4-2-3-5-19(17)18)12-14-6-9-16(21)10-7-14/h2-11,13H,12H2,1H3,(H,22,23)	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	2.40E+3	n/a	n/a	n/a	n/a	n/a	n/a
Rhône-Poulenc Rorer Curated by ChEMBL					Assay Description In vitro inhibitory concentration against rat prostaglandin G/H synthase 1				Bioorg Med Chem Lett 11: 2687-90 (2001) BindingDB Entry DOI: 10.7270/Q2BC3XV1
					More data for this Ligand-Target Pair