null

SMILES: O=C(Nc1cccnc1C(=O)NCC1CCOCC1)c1cccc2OCCOc12

InChI Key: InChIKey=NOPAIBYDUUIVJE-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50424485   

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))	BDBM50424485 (CHEMBL2316398) Show SMILES O=C(Nc1cccnc1C(=O)NCC1CCOCC1)c1cccc2OCCOc12 Show InChI InChI=1S/C21H23N3O5/c25-20(15-3-1-5-17-19(15)29-12-11-28-17)24-16-4-2-8-22-18(16)21(26)23-13-14-6-9-27-10-7-14/h1-5,8,14H,6-7,9-13H2,(H,23,26)(H,24,25)	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.20E+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))	BDBM50424485 (CHEMBL2316398) Show SMILES O=C(Nc1cccnc1C(=O)NCC1CCOCC1)c1cccc2OCCOc12 Show InChI InChI=1S/C21H23N3O5/c25-20(15-3-1-5-17-19(15)29-12-11-28-17)24-16-4-2-8-22-18(16)21(26)23-13-14-6-9-27-10-7-14/h1-5,8,14H,6-7,9-13H2,(H,23,26)(H,24,25)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	5.70E+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