Reaction Details |
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Target | Cannabinoid receptor 2 |
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Ligand | BDBM50256220 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_519287 (CHEMBL947739) |
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Ki | 5.8±n/a nM |
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Citation | Kai, H; Morioka, Y; Koriyama, Y; Okamoto, K; Hasegawa, Y; Hattori, M; Koike, K; Chiba, H; Shinohara, S; Iwamoto, Y; Takahashi, K; Tanimoto, N 2-Arylimino-5,6-dihydro-4H-1,3-thiazines as a new class of cannabinoid receptor agonists. Part 3: Synthesis and activity of isosteric analogs. Bioorg Med Chem Lett18:6444-7 (2008) [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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BDBM50256220 |
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n/a |
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Name | BDBM50256220 |
Synonyms: | CHEMBL475610 | S-methyl 3-(naphthalen-1-ylimino)-2-oxa-4-azaspiro[5.5]undecane-4-carbothioate |
Type | Small organic molecule |
Emp. Form. | C21H24N2O2S |
Mol. Mass. | 368.492 |
SMILES | CSC(=O)N1CC2(CCCCC2)CO\C1=N/c1cccc2ccccc12 |
Structure |
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