Reaction Details |
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Target | Cannabinoid receptor 1 |
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Ligand | BDBM50254163 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_560038 (CHEMBL1021558) |
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EC50 | 1650±n/a nM |
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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 |
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More Info.: | Get all data from this article, Assay Method |
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Cannabinoid receptor 1 |
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Name: | Cannabinoid receptor 1 |
Synonyms: | CANN6 | CANNABINOID CB1 | CB-R | CB1 | CNR | CNR1 | CNR1_HUMAN | Cannabinoid CB1 receptor | Cannabinoid receptor | Cannabinoid receptor 1 (CB1) | Cannabinoid receptor 1 (brain) |
Type: | G Protein-Coupled Receptor (GPCR) |
Mol. Mass.: | 52868.96 |
Organism: | Homo sapiens (Human) |
Description: | P21554 |
Residue: | 472 |
Sequence: | MKSILDGLADTTFRTITTDLLYVGSNDIQYEDIKGDMASKLGYFPQKFPLTSFRGSPFQE
KMTAGDNPQLVPADQVNITEFYNKSLSSFKENEENIQCGENFMDIECFMVLNPSQQLAIA
VLSLTLGTFTVLENLLVLCVILHSRSLRCRPSYHFIGSLAVADLLGSVIFVYSFIDFHVF
HRKDSRNVFLFKLGGVTASFTASVGSLFLTAIDRYISIHRPLAYKRIVTRPKAVVAFCLM
WTIAIVIAVLPLLGWNCEKLQSVCSDIFPHIDETYLMFWIGVTSVLLLFIVYAYMYILWK
AHSHAVRMIQRGTQKSIIIHTSEDGKVQVTRPDQARMDIRLAKTLVLILVVLIICWGPLL
AIMVYDVFGKMNKLIKTVFAFCSMLCLLNSTVNPIIYALRSKDLRHAFRSMFPSCEGTAQ
PLDNSMGDSDCLHKHANNAASVHRAAESCIKSTVKIAKVTMSVSTDTSAEAL
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BDBM50254163 |
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n/a |
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Name | BDBM50254163 |
Synonyms: | 2-(4-chlorophenylsulfonyl)-2-methyl-N-(5-o-tolyl-1,3,4-thiadiazol-2-yl)propanamide | CHEMBL461223 |
Type | Small organic molecule |
Emp. Form. | C19H18ClN3O3S2 |
Mol. Mass. | 435.948 |
SMILES | Cc1ccccc1-c1nnc(NC(=O)C(C)(C)S(=O)(=O)c2ccc(Cl)cc2)s1 |
Structure |
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