null

SMILES: CCCCn1c(C)c(C)cc(NC(=O)c2ccccc2F)c1=O

InChI Key: InChIKey=YPTSRSNJTLAXAS-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50431430   

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))	BDBM50431430 (CHEMBL2348275) Show SMILES CCCCn1c(C)c(C)cc(NC(=O)c2ccccc2F)c1=O Show InChI InChI=1S/C18H21FN2O2/c1-4-5-10-21-13(3)12(2)11-16(18(21)23)20-17(22)14-8-6-7-9-15(14)19/h6-9,11H,4-5,10H2,1-3H3,(H,20,22)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	88	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Shionogi Pharmaceutical Research Center Curated by ChEMBL					Assay Description Displacement of [H3]-CP-55940 from human recombinant CB2 receptor expressed in CHO cells				Bioorg Med Chem 21: 2045-55 (2013) Article DOI: 10.1016/j.bmc.2013.01.006 BindingDB Entry DOI: 10.7270/Q2PG1T2V
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM50431430 (CHEMBL2348275) Show SMILES CCCCn1c(C)c(C)cc(NC(=O)c2ccccc2F)c1=O Show InChI InChI=1S/C18H21FN2O2/c1-4-5-10-21-13(3)12(2)11-16(18(21)23)20-17(22)14-8-6-7-9-15(14)19/h6-9,11H,4-5,10H2,1-3H3,(H,20,22)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	617	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Shionogi Pharmaceutical Research Center Curated by ChEMBL					Assay Description Displacement of [H3]-CP-55940 from human recombinant CB1 receptor expressed in CHO cells				Bioorg Med Chem 21: 2045-55 (2013) Article DOI: 10.1016/j.bmc.2013.01.006 BindingDB Entry DOI: 10.7270/Q2PG1T2V
					More data for this Ligand-Target Pair