| Reaction Details |
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 | Report a problem with these data |
| Target | Cannabinoid receptor 2 |
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| Ligand | BDBM50156093 |
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| Substrate/Competitor | n/a |
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| Meas. Tech. | ChEMBL_1565590 (CHEMBL3782259) |
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| Ki | 11±n/a nM |
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| Citation |  Mugnaini, C; Brizzi, A; Ligresti, A; Allarà, M; Lamponi, S; Vacondio, F; Silva, C; Mor, M; Di Marzo, V; Corelli, F Investigations on the 4-Quinolone-3-carboxylic Acid Motif. 7. Synthesis and Pharmacological Evaluation of 4-Quinolone-3-carboxamides and 4-Hydroxy-2-quinolone-3-carboxamides as High Affinity Cannabinoid Receptor 2 (CB2R) Ligands with Improved Aqueous Solubility. J Med Chem59:1052-67 (2016) [PubMed] Article |
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| More Info.: | Get all data from this article, Assay Method |
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| Cannabinoid receptor 2 |
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| Name: | Cannabinoid receptor 2 |
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| Synonyms: | CANNABINOID CB2 | CB-2 | CB2 | CB2A | CB2B | CNR2 | CNR2_HUMAN | CX5 | Cannabinoid CB2 receptor | Cannabinoid receptor 2 (CB2) | Cannabinoid receptor 2 (CB2R) | hCB2 |
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| Type: | G Protein-Coupled Receptor (GPCR) |
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| Mol. Mass.: | 39690.94 |
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| Organism: | Homo sapiens (Human) |
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| Description: | P34972 |
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| Residue: | 360 |
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| Sequence: | MEECWVTEIANGSKDGLDSNPMKDYMILSGPQKTAVAVLCTLLGLLSALENVAVLYLILS
SHQLRRKPSYLFIGSLAGADFLASVVFACSFVNFHVFHGVDSKAVFLLKIGSVTMTFTAS
VGSLLLTAIDRYLCLRYPPSYKALLTRGRALVTLGIMWVLSALVSYLPLMGWTCCPRPCS
ELFPLIPNDYLLSWLLFIAFLFSGIIYTYGHVLWKAHQHVASLSGHQDRQVPGMARMRLD
VRLAKTLGLVLAVLLICWFPVLALMAHSLATTLSDQVKKAFAFCSMLCLINSMVNPVIYA
LRSGEIRSSAHHCLAHWKKCVRGLGSEAKEEAPRSSVTETEADGKITPWPDSRDLDLSDC
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| BDBM50156093 |
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| n/a |
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| Name | BDBM50156093 |
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| Synonyms: | CHEMBL3781965 |
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| Type | Small organic molecule |
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| Emp. Form. | C27H36FN3O2 |
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| Mol. Mass. | 453.592 |
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| SMILES | CC(C)c1cc2c(cc1F)n(CCN(C)C)cc(C(=O)NC13CC4CC(CC(C4)C1)C3)c2=O |TLB:28:27:30:24.23.22,28:23:30:27.29.26,THB:26:27:24.25.30:22,26:25:22:27.29.28| |
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| Structure | 
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