Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Cannabinoid receptor 2' and Ligand = 'BDBM50377704'   

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))	BDBM50377704 (CHEMBL255096) Show SMILES Cc1ccc(cc1S(=O)(=O)N1CCOCC1)C(=O)N[C@H]1CC2CC[C@@]1(C)C2(C)C |w:21.23,TLB:18:19:23.22:26| Show InChI InChI=1S/C22H32N2O4S/c1-15-5-6-16(13-18(15)29(26,27)24-9-11-28-12-10-24)20(25)23-19-14-17-7-8-22(19,4)21(17,2)3/h5-6,13,17,19H,7-12,14H2,1-4H3,(H,23,25)/t17?,19-,22+/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	8.10	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]CP-55940 from human cloned CB2 receptor				Bioorg Med Chem Lett 18: 2830-5 (2008) Article DOI: 10.1016/j.bmcl.2008.04.006 BindingDB Entry DOI: 10.7270/Q2P2701M
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM50377704 (CHEMBL255096) Show SMILES Cc1ccc(cc1S(=O)(=O)N1CCOCC1)C(=O)N[C@H]1CC2CC[C@@]1(C)C2(C)C |w:21.23,TLB:18:19:23.22:26| Show InChI InChI=1S/C22H32N2O4S/c1-15-5-6-16(13-18(15)29(26,27)24-9-11-28-12-10-24)20(25)23-19-14-17-7-8-22(19,4)21(17,2)3/h5-6,13,17,19H,7-12,14H2,1-4H3,(H,23,25)/t17?,19-,22+/m0/s1	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	14	n/a	n/a	n/a	n/a
Adolor Corporation Curated by ChEMBL					Assay Description Agonist activity at human cloned CB2 receptor by [35S]GTP-gamma-S binding assay				Bioorg Med Chem Lett 18: 2830-5 (2008) Article DOI: 10.1016/j.bmcl.2008.04.006 BindingDB Entry DOI: 10.7270/Q2P2701M
					More data for this Ligand-Target Pair