Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Cannabinoid receptor 2' and Ligand = 'BDBM50286064'   

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 (Rattus norvegicus (Rat))	BDBM50286064 (CHEMBL4174510) Show SMILES [H][C@@]12C[C@]1([H])c1c(C2)c(nn1-c1c[n+]([O-])ccn1)C(=O)N[C@H](CF)C(C)(C)C |r| Show InChI InChI=1S/C18H22FN5O2/c1-18(2,3)13(8-19)21-17(25)15-12-7-10-6-11(10)16(12)24(22-15)14-9-23(26)5-4-20-14/h4-5,9-11,13H,6-8H2,1-3H3,(H,21,25)/t10-,11-,13+/m0/s1	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	1.5	n/a	n/a	n/a	n/a
Arena Pharmaceuticals Curated by ChEMBL					Assay Description Agonist activity at recombinant rat CB2 receptor expressed in HEK293 cells assessed as increase in beta arrestin recruitment measured after 2 to 3 hr...				ACS Med Chem Lett 8: 1309-1313 (2017) Article DOI: 10.1021/acsmedchemlett.7b00396 BindingDB Entry DOI: 10.7270/Q25D8VCM
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM50286064 (CHEMBL4174510) Show SMILES [H][C@@]12C[C@]1([H])c1c(C2)c(nn1-c1c[n+]([O-])ccn1)C(=O)N[C@H](CF)C(C)(C)C |r| Show InChI InChI=1S/C18H22FN5O2/c1-18(2,3)13(8-19)21-17(25)15-12-7-10-6-11(10)16(12)24(22-15)14-9-23(26)5-4-20-14/h4-5,9-11,13H,6-8H2,1-3H3,(H,21,25)/t10-,11-,13+/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	1.20	n/a	n/a	n/a	n/a
Arena Pharmaceuticals Curated by ChEMBL					Assay Description Agonist activity at recombinant human CB2 receptor expressed in HEK293 cells assessed as increase in beta arrestin recruitment measured after 2 to 3 ...				ACS Med Chem Lett 8: 1309-1313 (2017) Article DOI: 10.1021/acsmedchemlett.7b00396 BindingDB Entry DOI: 10.7270/Q25D8VCM
					More data for this Ligand-Target Pair