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| Reaction Details | |||
|---|---|---|---|
 | Report a problem with these data | ||
| Target | Cannabinoid receptor 1 | ||
| Ligand | BDBM50160130 | ||
| Substrate/Competitor | n/a | ||
| Meas. Tech. | ChEMBL_305569 (CHEMBL827163) | ||
| IC50 | 2000±n/a nM | ||
| Citation |  Meurer, LC; Finke, PE; Mills, SG; Walsh, TF; Toupence, RB; Debenham, JS; Goulet, MT; Wang, J; Tong, X; Fong, TM; Lao, J; Schaeffer, MT; Chen, J; Shen, CP; Sloan Stribling, D; Shearman, LP; Strack, AM; Van der Ploeg, LH Synthesis and SAR of 5,6-diarylpyridines as human CB1 inverse agonists. Bioorg Med Chem Lett15:645-51 (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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| BDBM50160130 | |||
| n/a | |||
| Name | BDBM50160130 | ||
| Synonyms: | 1-Benzyl-5-(4-chloro-phenyl)-6-(2,4-dichloro-phenyl)-2-oxo-1,2-dihydro-pyridine-3-carbonitrile | CHEMBL178987 | ||
| Type | Small organic molecule | ||
| Emp. Form. | C25H15Cl3N2O | ||
| Mol. Mass. | 465.758 | ||
| SMILES | Clc1ccc(cc1)-c1cc(C#N)c(=O)n(Cc2ccccc2)c1-c1ccc(Cl)cc1Cl |(-6.98,-2.28,;-5.65,-1.5,;-5.65,.04,;-4.32,.8,;-2.97,.04,;-2.97,-1.5,;-4.3,-2.28,;-1.64,.8,;-1.64,2.35,;-.3,3.11,;-.3,4.67,;-.32,6.21,;1.04,2.35,;2.37,3.13,;1.04,.8,;2.37,.04,;3.7,.8,;3.7,2.35,;5.03,3.11,;6.37,2.35,;6.37,.8,;5.03,.04,;-.3,.04,;-.3,-1.5,;-1.64,-2.28,;-1.64,-3.82,;-.3,-4.59,;-.3,-6.13,;1.04,-3.82,;1.04,-2.28,;2.37,-1.5,)| | ||
| Structure | 
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