Reaction Details |
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Target | Cannabinoid receptor 1 |
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Ligand | BDBM50418021 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_728033 (CHEMBL1686904) |
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EC50 | 251.19±n/a nM |
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Citation | Kiyoi, T; Adam, JM; Clark, JK; Davies, K; Easson, AM; Edwards, D; Feilden, H; Fields, R; Francis, S; Jeremiah, F; McArthur, D; Morrison, AJ; Prosser, A; Ratcliffe, PD; Schulz, J; Wishart, G; Baker, J; Campbell, R; Cottney, JE; Deehan, M; Epemolu, O; Evans, L Discovery of potent and orally bioavailable heterocycle-based cannabinoid CB1 receptor agonists. Bioorg Med Chem Lett21:1748-53 (2011) [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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BDBM50418021 |
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n/a |
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Name | BDBM50418021 |
Synonyms: | CHEMBL1682274 |
Type | Small organic molecule |
Emp. Form. | C21H26ClN5O4 |
Mol. Mass. | 447.915 |
SMILES | CN(Cc1nc(no1)-c1cn(CC2CCOCC2)c2c(Cl)cccc12)[C@@H](CO)C(N)=O |r| |
Structure |
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