Compile Data Set for Download or QSAR

Found 2 hits of ec50 for monomerid = 50272174   

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
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM50272174 (3-(3-(3-Chlorophenyl)-1,2,4-oxadiazol-5-yl)-N-(9-e...) Show SMILES CCn1c2ccccc2c2cc(NC(=O)CCc3nc(no3)-c3cccc(Cl)c3)ccc12 Show InChI InChI=1S/C25H21ClN4O2/c1-2-30-21-9-4-3-8-19(21)20-15-18(10-11-22(20)30)27-23(31)12-13-24-28-25(29-32-24)16-6-5-7-17(26)14-16/h3-11,14-15H,2,12-13H2,1H3,(H,27,31)	PDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	410	n/a	n/a	n/a	n/a
Amgen Inc. Curated by ChEMBL					Assay Description Agonist activity at human recombinant CB2 receptor expressed in Sf9 cells by GTP-europium binding assay				J Med Chem 51: 5019-34 (2008) Article DOI: 10.1021/jm800463f BindingDB Entry DOI: 10.7270/Q2W096VS
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Homo sapiens (Human))	BDBM50272174 (3-(3-(3-Chlorophenyl)-1,2,4-oxadiazol-5-yl)-N-(9-e...) Show SMILES CCn1c2ccccc2c2cc(NC(=O)CCc3nc(no3)-c3cccc(Cl)c3)ccc12 Show InChI InChI=1S/C25H21ClN4O2/c1-2-30-21-9-4-3-8-19(21)20-15-18(10-11-22(20)30)27-23(31)12-13-24-28-25(29-32-24)16-6-5-7-17(26)14-16/h3-11,14-15H,2,12-13H2,1H3,(H,27,31)	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a
Amgen Inc. Curated by ChEMBL					Assay Description Agonist activity at human CB1 receptor expressed in Sf9 cells by GTP-europium binding assay				J Med Chem 51: 5019-34 (2008) Article DOI: 10.1021/jm800463f BindingDB Entry DOI: 10.7270/Q2W096VS
					More data for this Ligand-Target Pair