null

SMILES: CC(C)(C)c1nsc(NC(=O)[C@@H]2CCCN2C2CCOCC2)n1

InChI Key: InChIKey=WUUACLHVQQMLSF-LBPRGKRZSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50042668   

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
Cannabinoid receptor 1 (Homo sapiens (Human))	BDBM50042668 (CHEMBL3353872) Show SMILES CC(C)(C)c1nsc(NC(=O)[C@@H]2CCCN2C2CCOCC2)n1 |r| Show InChI InChI=1S/C16H26N4O2S/c1-16(2,3)14-18-15(23-19-14)17-13(21)12-5-4-8-20(12)11-6-9-22-10-7-11/h11-12H,4-10H2,1-3H3,(H,17,18,19,21)/t12-/m0/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	n/a	n/a	>2.00E+4	n/a	n/a	n/a	n/a
Boehringer Ingelheim Pharma GmbH& Co. KG Curated by ChEMBL					Assay Description Agonist activity at human CB1 receptor expressed in CHO cells assessed as inhibition of forskolin-stimulated cAMP production after 30 mins				Bioorg Med Chem Lett 25: 581-6 (2015) Article DOI: 10.1016/j.bmcl.2014.12.019 BindingDB Entry DOI: 10.7270/Q2CN75H1
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM50042668 (CHEMBL3353872) Show SMILES CC(C)(C)c1nsc(NC(=O)[C@@H]2CCCN2C2CCOCC2)n1 |r| Show InChI InChI=1S/C16H26N4O2S/c1-16(2,3)14-18-15(23-19-14)17-13(21)12-5-4-8-20(12)11-6-9-22-10-7-11/h11-12H,4-10H2,1-3H3,(H,17,18,19,21)/t12-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	n/a	n/a	100	n/a	n/a	n/a	n/a
Boehringer Ingelheim Pharma GmbH& Co. KG Curated by ChEMBL					Assay Description Agonist activity at human CB2 receptor expressed in CHO cells assessed as inhibition of forskolin-stimulated cAMP production after 30 mins				Bioorg Med Chem Lett 25: 581-6 (2015) Article DOI: 10.1016/j.bmcl.2014.12.019 BindingDB Entry DOI: 10.7270/Q2CN75H1
					More data for this Ligand-Target Pair