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SMILES: C[C@H]1C=C[C@@H](C)N1c1ccc(nn1)-c1cccc(Cl)c1Cl

InChI Key: InChIKey=SWMZUZLACLTWNE-PHIMTYICSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50415312   

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))	BDBM50415312 (CHEMBL594530) Show SMILES C[C@H]1C=C[C@@H](C)N1c1ccc(nn1)-c1cccc(Cl)c1Cl |r,c:2| Show InChI InChI=1S/C16H15Cl2N3/c1-10-6-7-11(2)21(10)15-9-8-14(19-20-15)12-4-3-5-13(17)16(12)18/h3-11H,1-2H3/t10-,11+	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	6.31E+3	n/a	n/a	n/a	n/a
GlaxoSmithKline Curated by ChEMBL					Assay Description Agonist activity at human CB1 receptor				Bioorg Med Chem Lett 20: 465-8 (2010) Article DOI: 10.1016/j.bmcl.2009.11.117 BindingDB Entry DOI: 10.7270/Q27M096D
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM50415312 (CHEMBL594530) Show SMILES C[C@H]1C=C[C@@H](C)N1c1ccc(nn1)-c1cccc(Cl)c1Cl |r,c:2| Show InChI InChI=1S/C16H15Cl2N3/c1-10-6-7-11(2)21(10)15-9-8-14(19-20-15)12-4-3-5-13(17)16(12)18/h3-11H,1-2H3/t10-,11+	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	0.631	n/a	n/a	n/a	n/a
GlaxoSmithKline Curated by ChEMBL					Assay Description Agonist activity at human CB2 receptor				Bioorg Med Chem Lett 20: 465-8 (2010) Article DOI: 10.1016/j.bmcl.2009.11.117 BindingDB Entry DOI: 10.7270/Q27M096D
					More data for this Ligand-Target Pair