BDBM50040942 CHEMBL3353841

SMILES: O=C(C1CC1)n1c2ccccc2c2nnc(SCc3ccccc3C#N)nc12

InChI Key: InChIKey=MAXCCXRICCMDDN-UHFFFAOYSA-N

Data: 1 EC50

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50040942   

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 2 (Homo sapiens (Human))	BDBM50040942 (CHEMBL3353841) Show SMILES O=C(C1CC1)n1c2ccccc2c2nnc(SCc3ccccc3C#N)nc12 Show InChI InChI=1S/C21H15N5OS/c22-11-14-5-1-2-6-15(14)12-28-21-23-19-18(24-25-21)16-7-3-4-8-17(16)26(19)20(27)13-9-10-13/h1-8,13H,9-10,12H2	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	181	n/a	n/a	n/a	n/a
University of Oxford Curated by ChEMBL					Assay Description Agonist activity at human CB2R expressed in CHO cells assessed as reduction in forskolin-induced cAMP accumulation by beta-galactosidase based comple...				Bioorg Med Chem 23: 241-63 (2014) Article DOI: 10.1016/j.bmc.2014.11.002 BindingDB Entry DOI: 10.7270/Q2930VS3
					More data for this Ligand-Target Pair