Reaction Details |
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Target | Cannabinoid receptor 1 |
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Ligand | BDBM50185037 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_342812 (CHEMBL868883) |
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Ki | 3500±n/a nM |
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Citation | Appendino, G; Minassi, A; Berton, L; Moriello, AS; Cascio, MG; De Petrocellis, L; Di Marzo, V Oxyhomologues of anandamide and related endolipids: chemoselective synthesis and biological activity. J Med Chem49:2333-8 (2006) [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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BDBM50185037 |
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n/a |
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Name | BDBM50185037 |
Synonyms: | CHEMBL203380 | O-arachidonoyl-N-(2-hydroxyethyl)hydroxylamine |
Type | Small organic molecule |
Emp. Form. | C22H37NO3 |
Mol. Mass. | 363.5341 |
SMILES | CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCC(=O)ONCCO |
Structure |
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