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| Reaction Details | |||
|---|---|---|---|
 | Report a problem with these data | ||
| Target | Cannabinoid receptor 1 | ||
| Ligand | BDBM50332881 | ||
| Substrate/Competitor | n/a | ||
| Meas. Tech. | ChEMBL_694005 (CHEMBL1636581) | ||
| Ki | 372.3±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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| BDBM50332881 | |||
| n/a | |||
| Name | BDBM50332881 | ||
| Synonyms: | 1-(2,4-Dichlorophenyl)-5-(2,5-dimethyl-1H-pyrrol-1-yl)-N-(5-hydroxypentyl)-4-methyl-1H-pyrazole-3-carboxamide | CHEMBL1631169 | ||
| Type | Small organic molecule | ||
| Emp. Form. | C22H26Cl2N4O2 | ||
| Mol. Mass. | 449.373 | ||
| SMILES | Cc1ccc(C)n1-c1c(C)c(nn1-c1ccc(Cl)cc1Cl)C(=O)NCCCCCO |(-3.67,-7.38,;-3.57,-8.93,;-4.76,-9.88,;-4.24,-11.31,;-2.7,-11.26,;-2.08,-12.19,;-2.28,-9.79,;-.87,-9.18,;-.32,-7.75,;-1.15,-6.44,;1.19,-7.82,;1.61,-9.29,;.34,-10.15,;.33,-11.7,;-1,-12.47,;-1,-14.01,;.34,-14.78,;.34,-16.32,;1.67,-14.01,;1.67,-12.46,;3.01,-11.68,;1.94,-6.45,;1.15,-5.15,;3.49,-6.42,;4.29,-7.73,;5.83,-7.68,;6.63,-9,;8.17,-8.96,;8.98,-10.28,;10.52,-10.24,)| | ||
| Structure | 
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