Reaction Details |
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Target | Cannabinoid receptor 1 |
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Ligand | BDBM50601131 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_2235849 (CHEMBL5149621) |
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Ki | >10000±n/a nM |
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Citation | Gado, F; Ferrisi, R; Polini, B; Mohamed, KA; Ricardi, C; Lucarini, E; Carpi, S; Domenichini, F; Stevenson, LA; Rapposelli, S; Saccomanni, G; Nieri, P; Ortore, G; Pertwee, RG; Ghelardini, C; Di Cesare Mannelli, L; Chiellini, G; Laprairie, RB; Manera, C Design, Synthesis, and Biological Activity of New CB2 Receptor Ligands: from Orthosteric and Allosteric Modulators to Dualsteric/Bitopic Ligands. J Med Chem65:9918-9938 (2022) [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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BDBM50601131 |
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n/a |
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Name | BDBM50601131 |
Synonyms: | CHEMBL5193398 |
Type | Small organic molecule |
Emp. Form. | C38H53Br2N7O4 |
Mol. Mass. | 831.68 |
SMILES | Cc1c(Br)cn(CCCc2cn(CCCCCn3c(C)c(Br)cc(C(=O)NC4CCCCCC4)c3=O)nn2)c(=O)c1NC(=O)C1CCCCCC1 |
Structure |
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