BDBM50040902 CHEMBL3353823

SMILES: [O-][N+](=O)c1ccccc1CSc1nnc2c(n1)[nH]c1cccc(Br)c21

InChI Key: InChIKey=KJQRYYOUOZACBV-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 = 50040902   

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))	BDBM50040902 (CHEMBL3353823) Show SMILES [O-][N+](=O)c1ccccc1CSc1nnc2c(n1)[nH]c1cccc(Br)c21 Show InChI InChI=1S/C16H10BrN5O2S/c17-10-5-3-6-11-13(10)14-15(18-11)19-16(21-20-14)25-8-9-4-1-2-7-12(9)22(23)24/h1-7H,8H2,(H,18,19,21)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	37	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