Reaction Details | |||
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Target | Cannabinoid receptor 2 | ||
Ligand | BDBM50082772 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | ChEMBL_1475933 (CHEMBL3425330) | ||
Ki | 7.4±n/a nM | ||
Citation | Manera, C; Malfitano, AM; Parkkari, T; Lucchesi, V; Carpi, S; Fogli, S; Bertini, S; Laezza, C; Ligresti, A; Saccomanni, G; Savinainen, JR; Ciaglia, E; Pisanti, S; Gazzerro, P; Di Marzo, V; Nieri, P; Macchia, M; Bifulco, M New quinolone- and 1,8-naphthyridine-3-carboxamides as selective CB2 receptor agonists with anticancer and immuno-modulatory activity. Eur J Med Chem97:10-8 (2015) [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: |
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BDBM50082772 | |||
n/a | |||
Name | BDBM50082772 | ||
Synonyms: | CHEMBL3422791 | ||
Type | Small organic molecule | ||
Emp. Form. | C22H30N4O4 | ||
Mol. Mass. | 414.498 | ||
SMILES | CC1CCC(CC1)NC(=O)c1c(O)c2cccnc2n(CCN2CCOCC2)c1=O |(9.06,6.01,;7.99,5.4,;6.66,6.17,;5.33,5.4,;5.33,3.86,;6.66,3.09,;7.99,3.86,;3.99,3.08,;3.99,1.54,;5.06,.93,;2.66,.77,;1.33,1.54,;1.33,2.77,;,.77,;-1.33,1.54,;-2.68,.77,;-2.68,-.77,;-1.33,-1.54,;,-.77,;1.33,-1.54,;1.33,-3.08,;2.67,-3.85,;2.67,-5.39,;4.01,-6.16,;4.01,-7.7,;2.67,-8.47,;1.34,-7.7,;1.34,-6.16,;2.66,-.77,;3.73,-1.38,)| | ||
Structure |