Reaction Details |
| Report a problem with these data |
Target | Cannabinoid receptor 2 |
---|
Ligand | BDBM50254147 |
---|
Substrate/Competitor | n/a |
---|
Meas. Tech. | ChEMBL_560040 (CHEMBL1021560) |
---|
EC50 | 25±n/a nM |
---|
Citation | Marx, IE; DiMauro, EF; Cheng, A; Emkey, R; Hitchcock, SA; Huang, L; Huang, MY; Human, J; Lee, JH; Li, X; Martin, MW; White, RD; Fremeau, RT; Patel, VF Discovery of alpha-amidosulfones as potent and selective agonists of CB2: synthesis, SAR, and pharmacokinetic properties. Bioorg Med Chem Lett19:31-5 (2008) [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: | MEECWVTEIANGSKDGLDSNPMKDYMILSGPQKTAVAVLCTLLGLLSALENVAVLYLILS
SHQLRRKPSYLFIGSLAGADFLASVVFACSFVNFHVFHGVDSKAVFLLKIGSVTMTFTAS
VGSLLLTAIDRYLCLRYPPSYKALLTRGRALVTLGIMWVLSALVSYLPLMGWTCCPRPCS
ELFPLIPNDYLLSWLLFIAFLFSGIIYTYGHVLWKAHQHVASLSGHQDRQVPGMARMRLD
VRLAKTLGLVLAVLLICWFPVLALMAHSLATTLSDQVKKAFAFCSMLCLINSMVNPVIYA
LRSGEIRSSAHHCLAHWKKCVRGLGSEAKEEAPRSSVTETEADGKITPWPDSRDLDLSDC
|
|
|
BDBM50254147 |
---|
n/a |
---|
Name | BDBM50254147 |
Synonyms: | CHEMBL467029 | N-(3-tert-butyl-1-methyl-1H-pyrazol-5-yl)-2-(4-chlorophenylsulfonyl)-2-methylpropanamide |
Type | Small organic molecule |
Emp. Form. | C18H24ClN3O3S |
Mol. Mass. | 397.919 |
SMILES | Cn1nc(cc1NC(=O)C(C)(C)S(=O)(=O)c1ccc(Cl)cc1)C(C)(C)C |
Structure |
|