Reaction Details |
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Target | Cannabinoid receptor 2 |
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Ligand | BDBM50543738 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1989775 (CHEMBL4623510) |
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Ki | 1.2±n/a nM |
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Citation | Brizzi, A; Aiello, F; Boccella, S; Cascio, MG; De Petrocellis, L; Frosini, M; Gado, F; Ligresti, A; Luongo, L; Marini, P; Mugnaini, C; Pessina, F; Corelli, F; Maione, S; Manera, C; Pertwee, RG; Di Marzo, V Synthetic bioactive olivetol-related amides: The influence of the phenolic group in cannabinoid receptor activity. Bioorg Med Chem28:0 (2020) [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 |
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: | MEECWVTEIANGSKDGLDSNPMKDYMILSGPQKTAVAVLCTLLGLLSALENVAVLYLILS
SHQLRRKPSYLFIGSLAGADFLASVVFACSFVNFHVFHGVDSKAVFLLKIGSVTMTFTAS
VGSLLLTAIDRYLCLRYPPSYKALLTRGRALVTLGIMWVLSALVSYLPLMGWTCCPRPCS
ELFPLIPNDYLLSWLLFIAFLFSGIIYTYGHVLWKAHQHVASLSGHQDRQVPGMARMRLD
VRLAKTLGLVLAVLLICWFPVLALMAHSLATTLSDQVKKAFAFCSMLCLINSMVNPVIYA
LRSGEIRSSAHHCLAHWKKCVRGLGSEAKEEAPRSSVTETEADGKITPWPDSRDLDLSDC
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BDBM50543738 |
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n/a |
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Name | BDBM50543738 |
Synonyms: | CHEMBL4644215 |
Type | Small organic molecule |
Emp. Form. | C26H43NO3 |
Mol. Mass. | 417.6245 |
SMILES | CCCCCc1cc(OC)cc(OCCCCCCCCCCC(=O)NC2CC2)c1 |
Structure |
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