Reaction Details | |||
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Target | Cannabinoid receptor 1 | ||
Ligand | BDBM50161582 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | ChEMBL_306671 (CHEMBL832272) | ||
IC50 | 46±n/a nM | ||
Citation | Plummer, CW; Finke, PE; Mills, SG; Wang, J; Tong, X; Doss, GA; Fong, TM; Lao, JZ; Schaeffer, MT; Chen, J; Shen, CP; Stribling, DS; Shearman, LP; Strack, AM; Van der Ploeg, LH Synthesis and activity of 4,5-diarylimidazoles as human CB1 receptor inverse agonists. Bioorg Med Chem Lett15:1441-6 (2005) [PubMed] Article | ||
More Info.: | Get all data from this article, Assay Method | ||
Cannabinoid receptor 1 | |||
Name: | Cannabinoid receptor 1 | ||
Synonyms: | CANN6 | CANNABINOID CB1 | CB-R | CB1 | CNR | CNR1 | CNR1_HUMAN | Cannabinoid CB1 receptor | Cannabinoid receptor | Cannabinoid receptor 1 (CB1) | Cannabinoid receptor 1 (brain) | ||
Type: | G Protein-Coupled Receptor (GPCR) | ||
Mol. Mass.: | 52868.96 | ||
Organism: | Homo sapiens (Human) | ||
Description: | P21554 | ||
Residue: | 472 | ||
Sequence: |
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BDBM50161582 | |||
n/a | |||
Name | BDBM50161582 | ||
Synonyms: | 4-(4-Chloro-phenyl)-5-(2,4-dichloro-phenyl)-1-methyl-1H-imidazole-2-carboxylic acid cyclohexylamide | CHEMBL368441 | ||
Type | Small organic molecule | ||
Emp. Form. | C23H22Cl3N3O | ||
Mol. Mass. | 462.799 | ||
SMILES | Cn1c(nc(c1-c1ccc(Cl)cc1Cl)-c1ccc(Cl)cc1)C(=O)NC1CCCCC1 |(-3.33,1.68,;-2.14,1.1,;-.62,2.17,;.64,1.3,;.21,-.17,;-1.34,-.22,;-2.09,-1.57,;-1.28,-2.88,;-2.03,-4.24,;-3.58,-4.25,;-4.33,-5.62,;-4.38,-2.95,;-3.61,-1.59,;-4.41,-.29,;1.01,-1.52,;2.55,-1.45,;3.34,-2.76,;2.61,-4.13,;3.41,-5.44,;1.06,-4.17,;.26,-2.83,;-.67,3.72,;-2.02,4.47,;.66,4.52,;2.01,3.82,;3.33,3.03,;4.66,3.79,;4.66,5.33,;3.32,6.1,;2.01,5.33,)| | ||
Structure |