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| Reaction Details | |||
|---|---|---|---|
 | Report a problem with these data | ||
| Target | Cannabinoid receptor 1 | ||
| Ligand | BDBM50258606 | ||
| Substrate/Competitor | n/a | ||
| Meas. Tech. | ChEMBL_523688 (CHEMBL997203) | ||
| Ki | 1600±n/a nM | ||
| Citation |  Manera, C; Saccomanni, G; Adinolfi, B; Benetti, V; Ligresti, A; Cascio, MG; Tuccinardi, T; Lucchesi, V; Martinelli, A; Nieri, P; Masini, E; Di Marzo, V; Ferrarini, PL Rational design, synthesis, and pharmacological properties of new 1,8-naphthyridin-2(1H)-on-3-carboxamide derivatives as highly selective cannabinoid-2 receptor agonists. J Med Chem52:3644-51 (2009) [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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| BDBM50258606 | |||
| n/a | |||
| Name | BDBM50258606 | ||
| Synonyms: | CHEMBL467476 | N-(4-Methylcyclohexyl)-1-benzyl-1,8-naphthyridin-2(1H)-on-3-carboxamide | ||
| Type | Small organic molecule | ||
| Emp. Form. | C23H25N3O2 | ||
| Mol. Mass. | 375.4635 | ||
| SMILES | CC1CCC(CC1)NC(=O)c1cc2cccnc2n(Cc2ccccc2)c1=O |(17.99,-33.21,;16.65,-33.98,;16.65,-35.52,;15.32,-36.29,;13.98,-35.51,;13.98,-33.98,;15.32,-33.21,;12.65,-36.28,;11.32,-35.51,;11.31,-33.97,;9.98,-36.29,;8.63,-35.51,;7.3,-36.3,;5.96,-35.54,;4.63,-36.31,;4.63,-37.85,;5.97,-38.62,;7.3,-37.85,;8.65,-38.62,;8.65,-40.16,;9.99,-40.92,;9.99,-42.45,;11.32,-43.22,;12.65,-42.44,;12.64,-40.91,;11.32,-40.16,;9.99,-37.84,;11.33,-38.61,)| | ||
| Structure | 
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