BDBM50388884 CHEMBL2063252

SMILES: Clc1ccc(cc1)-c1c2OCCCC(N3CCCC3=O)c2nn1-c1ccccc1Cl

InChI Key: InChIKey=FIICBAHGDUKACY-UHFFFAOYSA-N

Data: 3 KI

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 3 hits for monomerid = 50388884   

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))	BDBM50388884 (CHEMBL2063252) Show SMILES Clc1ccc(cc1)-c1c2OCCCC(N3CCCC3=O)c2nn1-c1ccccc1Cl Show InChI InChI=1S/C23H21Cl2N3O2/c24-16-11-9-15(10-12-16)22-23-21(26-28(22)18-6-2-1-5-17(18)25)19(7-4-14-30-23)27-13-3-8-20(27)29/h1-2,5-6,9-12,19H,3-4,7-8,13-14H2	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Displacement of [3H]SR141716A form human CB1 receptor expressed in HEK293 cells after 60 mins by beta counting				ACS Med Chem Lett 3: 397-401 (2012) Article DOI: 10.1021/ml3000325 BindingDB Entry DOI: 10.7270/Q22N53BD
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Homo sapiens (Human))	BDBM50388884 (CHEMBL2063252) Show SMILES Clc1ccc(cc1)-c1c2OCCCC(N3CCCC3=O)c2nn1-c1ccccc1Cl Show InChI InChI=1S/C23H21Cl2N3O2/c24-16-11-9-15(10-12-16)22-23-21(26-28(22)18-6-2-1-5-17(18)25)19(7-4-14-30-23)27-13-3-8-20(27)29/h1-2,5-6,9-12,19H,3-4,7-8,13-14H2	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	6.5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Antagonist activity at human CB1 receptor expressed in CHO-K1 cells assessed as inhibition of CP-55940-induced [35S]GTPgammaS binding incubated for 1...				ACS Med Chem Lett 3: 397-401 (2012) Article DOI: 10.1021/ml3000325 BindingDB Entry DOI: 10.7270/Q22N53BD
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM50388884 (CHEMBL2063252) Show SMILES Clc1ccc(cc1)-c1c2OCCCC(N3CCCC3=O)c2nn1-c1ccccc1Cl Show InChI InChI=1S/C23H21Cl2N3O2/c24-16-11-9-15(10-12-16)22-23-21(26-28(22)18-6-2-1-5-17(18)25)19(7-4-14-30-23)27-13-3-8-20(27)29/h1-2,5-6,9-12,19H,3-4,7-8,13-14H2	PDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	7.56E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Displacement of [3H]CP-55940 from human CB2 receptor expressed in CHO-K1 cells after 60 mins by beta counting				ACS Med Chem Lett 3: 397-401 (2012) Article DOI: 10.1021/ml3000325 BindingDB Entry DOI: 10.7270/Q22N53BD
					More data for this Ligand-Target Pair