null

SMILES: O=C(NCC1CCCCC1)c1ccncc1NC(=O)c1cccc2ccccc12

InChI Key: InChIKey=ZSPFVMNLOUVHDD-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50424487   

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))	BDBM50424487 (CHEMBL2316394) Show SMILES O=C(NCC1CCCCC1)c1ccncc1NC(=O)c1cccc2ccccc12 Show InChI InChI=1S/C24H25N3O2/c28-23(26-15-17-7-2-1-3-8-17)21-13-14-25-16-22(21)27-24(29)20-12-6-10-18-9-4-5-11-19(18)20/h4-6,9-14,16-17H,1-3,7-8,15H2,(H,26,28)(H,27,29)	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.60E+3	n/a	n/a	n/a	n/a	n/a	n/a
AstraZeneca Curated by ChEMBL					Assay Description Displacement of [3H]-CP55,940 from human CB1 receptor expressed in HEK293S cell membranes by scintillation counting analysis				J Med Chem 56: 220-40 (2013) Article DOI: 10.1021/jm301511h BindingDB Entry DOI: 10.7270/Q2057H7B
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM50424487 (CHEMBL2316394) Show SMILES O=C(NCC1CCCCC1)c1ccncc1NC(=O)c1cccc2ccccc12 Show InChI InChI=1S/C24H25N3O2/c28-23(26-15-17-7-2-1-3-8-17)21-13-14-25-16-22(21)27-24(29)20-12-6-10-18-9-4-5-11-19(18)20/h4-6,9-14,16-17H,1-3,7-8,15H2,(H,26,28)(H,27,29)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>8.90E+3	n/a	n/a	n/a	n/a	n/a	n/a
AstraZeneca Curated by ChEMBL					Assay Description Displacement of [3H]-CP55,940 from human CB2 receptor expressed in Sf9 cell membranes by scintillation counting analysis				J Med Chem 56: 220-40 (2013) Article DOI: 10.1021/jm301511h BindingDB Entry DOI: 10.7270/Q2057H7B
					More data for this Ligand-Target Pair