null

SMILES: CCCCc1ccc(CN(Cc2ccccc2OCC(O)=O)S(C)(=O)=O)cc1

InChI Key: InChIKey=VBBRFPKXFMMYOB-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50293508   

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 E2 receptor EP4 subtype (Rattus norvegicus)	BDBM50293508 (2-(2-((N-(4-butylbenzyl)methylsulfonamido)methyl)p...) Show SMILES CCCCc1ccc(CN(Cc2ccccc2OCC(O)=O)S(C)(=O)=O)cc1 Show InChI InChI=1S/C21H27NO5S/c1-3-4-7-17-10-12-18(13-11-17)14-22(28(2,25)26)15-19-8-5-6-9-20(19)27-16-21(23)24/h5-6,8-13H,3-4,7,14-16H2,1-2H3,(H,23,24)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	>3.20E+3	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer Global Research and Development Curated by ChEMBL					Assay Description Inhibition of rat EP4 receptor expressed in HEK293 cells				Bioorg Med Chem Lett 19: 2075-8 (2009) Article DOI: 10.1016/j.bmcl.2009.01.059 BindingDB Entry DOI: 10.7270/Q2PR7W18
					More data for this Ligand-Target Pair
Prostaglandin E2 receptor EP2 subtype (Rattus norvegicus)	BDBM50293508 (2-(2-((N-(4-butylbenzyl)methylsulfonamido)methyl)p...) Show SMILES CCCCc1ccc(CN(Cc2ccccc2OCC(O)=O)S(C)(=O)=O)cc1 Show InChI InChI=1S/C21H27NO5S/c1-3-4-7-17-10-12-18(13-11-17)14-22(28(2,25)26)15-19-8-5-6-9-20(19)27-16-21(23)24/h5-6,8-13H,3-4,7,14-16H2,1-2H3,(H,23,24)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.20E+3	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer Global Research and Development Curated by ChEMBL					Assay Description Inhibition of rat EP2 receptor expressed in HEK293 cells				Bioorg Med Chem Lett 19: 2075-8 (2009) Article DOI: 10.1016/j.bmcl.2009.01.059 BindingDB Entry DOI: 10.7270/Q2PR7W18
					More data for this Ligand-Target Pair