Compile Data Set for Download or QSAR

Found 2 hits of ic50 for monomerid = 50303669   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kJ/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Prostaglandin E2 receptor EP3 subtype (Homo sapiens (Human))	BDBM50303669 (CHEMBL567266 | Naphthalene-2-carboxylic acid{4-[(E...) Show SMILES CN1C(=O)C(NC(=O)c2ccc3ccccc3c2)c2c1cccc2\C=C\C(=O)NS(=O)(=O)c1cc(Cl)c(Cl)s1 Show InChI InChI=1S/C27H19Cl2N3O5S2/c1-32-20-8-4-7-16(11-12-21(33)31-39(36,37)22-14-19(28)25(29)38-22)23(20)24(27(32)35)30-26(34)18-10-9-15-5-2-3-6-17(15)13-18/h2-14,24H,1H3,(H,30,34)(H,31,33)/b12-11+	PDB KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	14.6	n/a	n/a	n/a	n/a	n/a	n/a
deCODE Chemistry, Inc. Curated by ChEMBL					Assay Description Displacement of [3H]PGE2 from human EP3 receptor after 1 hr by liquid scintillation counting				J Med Chem 53: 18-36 (2010) Article DOI: 10.1021/jm9005912 BindingDB Entry DOI: 10.7270/Q2XP752H
					More data for this Ligand-Target Pair
Prostaglandin E2 receptor EP3 subtype (Homo sapiens (Human))	BDBM50303669 (CHEMBL567266 | Naphthalene-2-carboxylic acid{4-[(E...) Show SMILES CN1C(=O)C(NC(=O)c2ccc3ccccc3c2)c2c1cccc2\C=C\C(=O)NS(=O)(=O)c1cc(Cl)c(Cl)s1 Show InChI InChI=1S/C27H19Cl2N3O5S2/c1-32-20-8-4-7-16(11-12-21(33)31-39(36,37)22-14-19(28)25(29)38-22)23(20)24(27(32)35)30-26(34)18-10-9-15-5-2-3-6-17(15)13-18/h2-14,24H,1H3,(H,30,34)(H,31,33)/b12-11+	PDB KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.25E+3	n/a	n/a	n/a	n/a	n/a	n/a
deCODE Chemistry, Inc. Curated by ChEMBL					Assay Description Displacement of [3H]PGE2 from human EP3 receptor after 1 hr by liquid scintillation counting in presence of 10% human serum				J Med Chem 53: 18-36 (2010) Article DOI: 10.1021/jm9005912 BindingDB Entry DOI: 10.7270/Q2XP752H
					More data for this Ligand-Target Pair