Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Cannabinoid receptor 2' and Ligand = 'BDBM50277227'   

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))	BDBM50277227 (4-(5-(5-(cyclohexylmethyl)-1H-1,2,4-triazol-3-yl)-...) Show SMILES Cc1ccc(cc1S(=O)(=O)N1CCOCC1)-c1nnc(CC2CCCCC2)[nH]1 Show InChI InChI=1S/C20H28N4O3S/c1-15-7-8-17(14-18(15)28(25,26)24-9-11-27-12-10-24)20-21-19(22-23-20)13-16-5-3-2-4-6-16/h7-8,14,16H,2-6,9-13H2,1H3,(H,21,22,23)	PDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	27	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Adolor Corporation Curated by ChEMBL					Assay Description Displacement of [3H]CP55940 from human cloned CB2 receptor by scintillation spectrometry				Bioorg Med Chem Lett 19: 309-13 (2008) Article DOI: 10.1016/j.bmcl.2008.11.091 BindingDB Entry DOI: 10.7270/Q2G73DK3
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM50277227 (4-(5-(5-(cyclohexylmethyl)-1H-1,2,4-triazol-3-yl)-...) Show SMILES Cc1ccc(cc1S(=O)(=O)N1CCOCC1)-c1nnc(CC2CCCCC2)[nH]1 Show InChI InChI=1S/C20H28N4O3S/c1-15-7-8-17(14-18(15)28(25,26)24-9-11-27-12-10-24)20-21-19(22-23-20)13-16-5-3-2-4-6-16/h7-8,14,16H,2-6,9-13H2,1H3,(H,21,22,23)	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	57	n/a	n/a	n/a	n/a
Adolor Corporation Curated by ChEMBL					Assay Description Agonist activity at human cloned CB2 receptor assessed as stimulation of [35S]GTPgammaS binding				Bioorg Med Chem Lett 19: 309-13 (2008) Article DOI: 10.1016/j.bmcl.2008.11.091 BindingDB Entry DOI: 10.7270/Q2G73DK3
					More data for this Ligand-Target Pair