BDBM50394645 CHEMBL2164609

SMILES: COc1cc(C\C=C\c2ccccc2\C=C\C(=O)NS(=O)(=O)c2cccs2)ccc1OCCn1cc2ccccc2c1C#N

InChI Key: InChIKey=VPTIIMVBILWEMO-IKSXBEDHSA-N

Data: 4 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 4 hits for monomerid = 50394645   

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))	BDBM50394645 (CHEMBL2164609) Show SMILES COc1cc(C\C=C\c2ccccc2\C=C\C(=O)NS(=O)(=O)c2cccs2)ccc1OCCn1cc2ccccc2c1C#N Show InChI InChI=1S/C34H29N3O5S2/c1-41-32-22-25(15-17-31(32)42-20-19-37-24-28-11-4-5-13-29(28)30(37)23-35)8-6-12-26-9-2-3-10-27(26)16-18-33(38)36-44(39,40)34-14-7-21-43-34/h2-7,9-18,21-22,24H,8,19-20H2,1H3,(H,36,38)/b12-6+,18-16+	PDB KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	26	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Displacement of [3H]PGE2 from human EP3R expressed in chem1 cells after 2hrs by beta counting				ACS Med Chem Lett 3: 774-779 (2012) Article DOI: 10.1021/ml300191g BindingDB Entry DOI: 10.7270/Q2DZ09D3
					More data for this Ligand-Target Pair
Prostaglandin E2 receptor EP4 subtype (Homo sapiens (Human))	BDBM50394645 (CHEMBL2164609) Show SMILES COc1cc(C\C=C\c2ccccc2\C=C\C(=O)NS(=O)(=O)c2cccs2)ccc1OCCn1cc2ccccc2c1C#N Show InChI InChI=1S/C34H29N3O5S2/c1-41-32-22-25(15-17-31(32)42-20-19-37-24-28-11-4-5-13-29(28)30(37)23-35)8-6-12-26-9-2-3-10-27(26)16-18-33(38)36-44(39,40)34-14-7-21-43-34/h2-7,9-18,21-22,24H,8,19-20H2,1H3,(H,36,38)/b12-6+,18-16+	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	9.45E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Displacement of [3H]PGE2 from human EP4R expressed in chem1 cells after 2hrs by beta counting				ACS Med Chem Lett 3: 774-779 (2012) Article DOI: 10.1021/ml300191g BindingDB Entry DOI: 10.7270/Q2DZ09D3
					More data for this Ligand-Target Pair
Prostaglandin E2 receptor EP2 subtype (Homo sapiens (Human))	BDBM50394645 (CHEMBL2164609) Show SMILES COc1cc(C\C=C\c2ccccc2\C=C\C(=O)NS(=O)(=O)c2cccs2)ccc1OCCn1cc2ccccc2c1C#N Show InChI InChI=1S/C34H29N3O5S2/c1-41-32-22-25(15-17-31(32)42-20-19-37-24-28-11-4-5-13-29(28)30(37)23-35)8-6-12-26-9-2-3-10-27(26)16-18-33(38)36-44(39,40)34-14-7-21-43-34/h2-7,9-18,21-22,24H,8,19-20H2,1H3,(H,36,38)/b12-6+,18-16+	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	1.08E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Displacement of [3H]PGE2 from human EP2R expressed in chem1 cells after 2hrs by beta counting				ACS Med Chem Lett 3: 774-779 (2012) Article DOI: 10.1021/ml300191g BindingDB Entry DOI: 10.7270/Q2DZ09D3
					More data for this Ligand-Target Pair
Prostaglandin E2 receptor EP1 subtype (EP1) (Homo sapiens (Human))	BDBM50394645 (CHEMBL2164609) Show SMILES COc1cc(C\C=C\c2ccccc2\C=C\C(=O)NS(=O)(=O)c2cccs2)ccc1OCCn1cc2ccccc2c1C#N Show InChI InChI=1S/C34H29N3O5S2/c1-41-32-22-25(15-17-31(32)42-20-19-37-24-28-11-4-5-13-29(28)30(37)23-35)8-6-12-26-9-2-3-10-27(26)16-18-33(38)36-44(39,40)34-14-7-21-43-34/h2-7,9-18,21-22,24H,8,19-20H2,1H3,(H,36,38)/b12-6+,18-16+	KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	2.03E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Displacement of [3H]PGE2 from human EP1R expressed in chem1 cells after 2hrs by beta counting				ACS Med Chem Lett 3: 774-779 (2012) Article DOI: 10.1021/ml300191g BindingDB Entry DOI: 10.7270/Q2DZ09D3
					More data for this Ligand-Target Pair