Reaction Details |
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Target | Cannabinoid receptor 2 |
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Ligand | BDBM50234380 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_462576 (CHEMBL928502) |
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Ki | 4±n/a nM |
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Citation | Ermann, M; Riether, D; Walker, ER; Mushi, IF; Jenkins, JE; Noya-Marino, B; Brewer, ML; Taylor, MG; Amouzegh, P; East, SP; Dymock, BW; Gemkow, MJ; Kahrs, AF; Ebneth, A; Löbbe, S; O'Shea, K; Shih, DT; Thomson, D Arylsulfonamide CB2 receptor agonists: SAR and optimization of CB2 selectivity. Bioorg Med Chem Lett18:1725-9 (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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BDBM50234380 |
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n/a |
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Name | BDBM50234380 |
Synonyms: | CHEMBL245876 | quinolin-8-yl 4-methyl-3-(piperidin-1-ylsulfonyl)benzoate |
Type | Small organic molecule |
Emp. Form. | C22H22N2O4S |
Mol. Mass. | 410.486 |
SMILES | Cc1ccc(cc1S(=O)(=O)N1CCCCC1)C(=O)Oc1cccc2cccnc12 |
Structure |
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