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| Reaction Details | |||
|---|---|---|---|
 | Report a problem with these data | ||
| Target | Cannabinoid receptor 2 | ||
| Ligand | BDBM50332882 | ||
| Substrate/Competitor | n/a | ||
| Meas. Tech. | ChEMBL_694006 (CHEMBL1636582) | ||
| Ki | 487.3±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 2 | |||
| Name: | Cannabinoid receptor 2 | ||
| Synonyms: | CANNABINOID CB2 | CB-2 | CB2 | CB2A | CB2B | CNR2 | CNR2_HUMAN | CX5 | Cannabinoid CB2 receptor | Cannabinoid receptor 2 (CB2) | Cannabinoid receptor 2 (CB2R) | hCB2 | ||
| Type: | G Protein-Coupled Receptor (GPCR) | ||
| Mol. Mass.: | 39690.94 | ||
| Organism: | Homo sapiens (Human) | ||
| Description: | P34972 | ||
| Residue: | 360 | ||
| Sequence: |
| ||
| BDBM50332882 | |||
| n/a | |||
| Name | BDBM50332882 | ||
| Synonyms: | 1-(2,4-Difluorophenyl)-5-(2,5-dimethyl-1H-pyrrol-1-yl)-Nhexyl-4-methyl-1H-pyrazole-3-carboxamide | CHEMBL1631290 | ||
| Type | Small organic molecule | ||
| Emp. Form. | C23H28F2N4O | ||
| Mol. Mass. | 414.4914 | ||
| SMILES | CCCCCCNC(=O)c1nn(c(c1C)-n1c(C)ccc1C)-c1ccc(F)cc1F |(11.99,-5.89,;10.45,-5.88,;9.69,-4.55,;8.15,-4.54,;7.38,-3.2,;5.84,-3.2,;5.08,-1.87,;3.53,-1.86,;2.77,-.54,;2.74,-3.21,;3.16,-4.68,;1.89,-5.53,;.68,-4.57,;1.23,-3.14,;.39,-1.83,;-.75,-5.12,;-2.01,-4.21,;-2.05,-2.66,;-3.23,-5.12,;-2.77,-6.57,;-1.22,-6.57,;-.53,-7.48,;1.88,-7.08,;.55,-7.85,;.55,-9.4,;1.89,-10.17,;1.89,-11.71,;3.22,-9.4,;3.22,-7.85,;4.56,-7.06,)| | ||
| Structure | 
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