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| Reaction Details | |||
|---|---|---|---|
 | Report a problem with these data | ||
| Target | Cannabinoid receptor 1 | ||
| Ligand | BDBM50332879 | ||
| Substrate/Competitor | n/a | ||
| Meas. Tech. | ChEMBL_694005 (CHEMBL1636581) | ||
| Ki | 123.1±n/a nM | ||
| Citation |  Silvestri, R; Ligresti, A; La Regina, G; Piscitelli, F; Gatti, V; Lavecchia, A; Brizzi, A; Pasquini, S; Allarà, M; Fantini, N; Carai, MA; Bigogno, C; Rozio, MG; Sinisi, R; Novellino, E; Colombo, G; Di Marzo, V; Dondio, G; Corelli, F Synthesis and biological evaluation of new N-alkyl 1-aryl-5-(1H-pyrrol-1-yl)-1H-pyrazole-3-carboxamides as cannabinoid receptor ligands. Eur J Med Chem45:5878-86 (2010) [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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| BDBM50332879 | |||
| n/a | |||
| Name | BDBM50332879 | ||
| Synonyms: | CHEMBL1631167 | N-Butyl-1-(2,4-dichlorophenyl)-5-(2,5-dimethyl-1H-pyrrol-1-yl)-4-methyl-1H-pyrazole-3-carboxamide | ||
| Type | Small organic molecule | ||
| Emp. Form. | C21H24Cl2N4O | ||
| Mol. Mass. | 419.347 | ||
| SMILES | CCCCNC(=O)c1nn(c(c1C)-n1c(C)ccc1C)-c1ccc(Cl)cc1Cl |(19.07,-3.28,;17.53,-3.31,;16.73,-1.97,;15.21,-1.99,;14.42,-.67,;12.88,-.7,;12.09,.63,;12.13,-2.03,;12.62,-3.47,;11.39,-4.39,;10.13,-3.5,;10.6,-2.04,;9.69,-.79,;8.67,-3.99,;8.21,-5.44,;9.11,-6.69,;6.66,-5.45,;6.18,-4,;7.4,-3.09,;7.39,-1.55,;11.41,-5.94,;10.08,-6.73,;10.1,-8.26,;11.44,-9.03,;11.45,-10.57,;12.77,-8.24,;12.75,-6.69,;14.07,-5.91,)| | ||
| Structure | 
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