Reaction Details |
![](/images/Email.png) | Report a problem with these data |
Target | Cannabinoid receptor 1 |
---|
Ligand | BDBM50516297 |
---|
Substrate/Competitor | n/a |
---|
Meas. Tech. | ChEMBL_1864128 (CHEMBL4365103) |
---|
Ki | >10000±n/a nM |
---|
Citation | Montanari, S; Mahmoud, AM; Pruccoli, L; Rabbito, A; Naldi, M; Petralla, S; Moraleda, I; Bartolini, M; Monti, B; Iriepa, I; Belluti, F; Gobbi, S; Di Marzo, V; Bisi, A; Tarozzi, A; Ligresti, A; Rampa, A Discovery of novel benzofuran-based compounds with neuroprotective and immunomodulatory properties for Alzheimer's disease treatment. Eur J Med Chem178:243-258 (2019) [PubMed] Article |
---|
More Info.: | Get all data from this article, Assay Method |
---|
|
Cannabinoid receptor 1 |
---|
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
|
|
|
BDBM50516297 |
---|
n/a |
---|
Name | BDBM50516297 |
Synonyms: | CHEMBL4537149 |
Type | Small organic molecule |
Emp. Form. | C30H25NO4 |
Mol. Mass. | 463.5238 |
SMILES | COc1ccc(CNc2ccc(cc2)C(=O)c2c(oc3ccccc23)-c2ccc(OC)cc2)cc1 |
Structure |
|