Reaction Details |
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Target | Cannabinoid receptor 1 |
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Ligand | BDBM86538 |
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Substrate/Competitor | n/a |
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Ki | 5600±n/a nM |
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Comments | PDSP_4179 |
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Citation | Appendino, G; De Petrocellis, L; Trevisani, M; Minassi, A; Daddario, N; Moriello, AS; Gazzieri, D; Ligresti, A; Campi, B; Fontana, G; Pinna, C; Geppetti, P; Di Marzo, V Development of the first ultra-potent "capsaicinoid" agonist at transient receptor potential vanilloid type 1 (TRPV1) channels and its therapeutic potential. J Pharmacol Exp Ther312:561-70 (2005) [PubMed] Article |
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More Info.: | Get all data from this article |
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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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BDBM86538 |
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n/a |
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Name | BDBM86538 |
Synonyms: | PhAR, Cycloproyl |
Type | Small organic molecule |
Emp. Form. | C26H43NO4 |
Mol. Mass. | 433.6239 |
SMILES | CCCCCCCCC1OC1CCCCCCCC(=O)NCc1ccc(O)c(OC)c1 |
Structure |
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