null

SMILES: OC(=O)Cc1sc(COc2ccc(Cl)cc2)nc1-c1ccc(Cl)cc1

InChI Key: InChIKey=MYIQJEVYQYVXCY-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50309265   

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 D2 receptor 2 (Homo sapiens (Human))	BDBM50309265 (2-(2-((4-chlorophenoxy)methyl)-4-(4-chlorophenyl)t...) Show SMILES OC(=O)Cc1sc(COc2ccc(Cl)cc2)nc1-c1ccc(Cl)cc1 Show InChI InChI=1S/C18H13Cl2NO3S/c19-12-3-1-11(2-4-12)18-15(9-17(22)23)25-16(21-18)10-24-14-7-5-13(20)6-8-14/h1-8H,9-10H2,(H,22,23)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	370	n/a	n/a	n/a	n/a	n/a	n/a
7TM Pharma A/S Curated by ChEMBL					Assay Description Antagonist activity at human CRTH2 receptor expressed in HEK285-7 cells assessed as inhibition of beta arrestin translocation by bioluminescence reso...				Bioorg Med Chem Lett 20: 1181-5 (2010) Article DOI: 10.1016/j.bmcl.2009.12.015 BindingDB Entry DOI: 10.7270/Q2PR7W35
					More data for this Ligand-Target Pair
Prostaglandin D2 receptor 2 (Homo sapiens (Human))	BDBM50309265 (2-(2-((4-chlorophenoxy)methyl)-4-(4-chlorophenyl)t...) Show SMILES OC(=O)Cc1sc(COc2ccc(Cl)cc2)nc1-c1ccc(Cl)cc1 Show InChI InChI=1S/C18H13Cl2NO3S/c19-12-3-1-11(2-4-12)18-15(9-17(22)23)25-16(21-18)10-24-14-7-5-13(20)6-8-14/h1-8H,9-10H2,(H,22,23)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	32	n/a	n/a	n/a	n/a	n/a	n/a
7TM Pharma A/S Curated by ChEMBL					Assay Description Displacement of[3H]PGD2 from human CRTH2 receptor expressed in HEK385-7 cells				Bioorg Med Chem Lett 20: 1181-5 (2010) Article DOI: 10.1016/j.bmcl.2009.12.015 BindingDB Entry DOI: 10.7270/Q2PR7W35
					More data for this Ligand-Target Pair