BDBM50417222 CHEMBL1271971

SMILES: COc1ccc(Cn2cccc(NC(=O)Nc3cccc(OC)c3)c2=O)cc1

InChI Key: InChIKey=IXALCMDXGSZDGO-UHFFFAOYSA-N

Data: 1 KI

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50417222   

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 (Homo sapiens (Human))	BDBM50417222 (CHEMBL1271971) Show SMILES COc1ccc(Cn2cccc(NC(=O)Nc3cccc(OC)c3)c2=O)cc1 Show InChI InChI=1S/C21H21N3O4/c1-27-17-10-8-15(9-11-17)14-24-12-4-7-19(20(24)25)23-21(26)22-16-5-3-6-18(13-16)28-2/h3-13H,14H2,1-2H3,(H2,22,23,26)	PDB KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	794	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
GlaxoSmithKline Pharmaceuticals Curated by ChEMBL					Assay Description Antagonist activity at human EP3 receptor expressed in human U2OS cells assessed as inhibition of PGE2-induced intracellular calcium mobilization by ...				Bioorg Med Chem Lett 20: 6744-7 (2010) Article DOI: 10.1016/j.bmcl.2010.08.137 BindingDB Entry DOI: 10.7270/Q25M65Z8
					More data for this Ligand-Target Pair