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25I-NBOMe — Википедия

To explore a different substance…. Braden, MR. Towards a biophysical understanding of hallucinogen action. Imaging , 1 Apr , 38 4 , — Heim, R. Synthesis and pharmacology of potent 5-HT 2A receptor agonists with N methoxybenzyl partial structure. Structure-activity relationships of phenylalkylamines as agonist ligands for 5-HT 2A receptors. ChemMedChem , 15 Sep , 3 9 , — JW, Personal communication of unpublished research. Molecular interaction of serotonin 5-HT 2A receptor residues Phe 6. Theoretical studies on the interaction of partial agonists with the 5-HT 2A receptor. Aided Mol. Silva, ME. Theoretical study of the interaction of agonists with the 5-HT 2A receptor. Hansen, M. Design and synthesis of selective serotonin receptor agonists for positron emission tomography imaging of the brain. Thesis , University of Copenhagen, 16 Dec Parrish, JC. Toward a molecular understanding of hallucinogen action. Characterization of eleven 2,5-dimethoxy- N - 2-methoxybenzyl phenethylamine NBOMe derivatives and differentiation from their 3- and 4-methoxybenzyl analogues—Part I. Microgram J. Heim, R; Elz, S. Novel extremely potent partial 5-HT 2A -receptor agonists: Successful application of a new structure-activity concept. Poster abstract. Stereoselective synthesis, absolute configuration and 5-HT 2A -receptor agonism of chiral 2-methoxybenzylamines. Correlating the metabolic stability of psychedelic 5-HT 2A agonists with anecdotal reports of human oral bioavailability. N -Benzylmethoxytryptamines as potent serotonin 5-HT 2 receptor family agonists and comparison with a series of phenethylamine analogues. ACS Chem. Analytical characterization of bioactive N -benzyl-substituted phenethylamines and 5-methoxytryptamines. Rapid Commun. Mass Spectrom. Supplementary Data. Characterization of eleven 2,5-dimethoxy- N - 2-methoxybenzyl phenethylamine NBOMe derivatives and differentiation from their 3-and 4-methoxybenzyl analogues - Part II. Forensic Toxicol. Drug Test. Halberstadt, AL. Effects of the hallucinogen 2,5-dimethoxyiodophenethylamine 2C-I and superpotent N -benzyl derivatives on the head twitch response. Neuropharmacology , 1 Feb , 77 , — Hyperlab new compounds. Note: Contains links to hyperlab. Is LSD toxic? Forensic Sci. Detailed characterization of the in vitro pharmacological and pharmacokinetic properties of N - 2-hydroxybenzyl -2,5-dimethoxycyanophenylethylamine 25CN-NBOH , a highly selective and brain-penetrant 5-HT 2A receptor agonist. Receptor interaction profiles of novel N methoxybenzyl NBOMe derivatives of 2,5-dimethoxy-substituted phenethylamines 2C drugs. Neuropharmacology , 1 Dec , 99 — Analysis of synthetic phenethylamine street drugs using direct sample analysis coupled to accurate mass time of flight mass spectrometry. Zawilska, JB; Andrzejczak, D. Next generation of novel psychoactive substances on the horizon — A complex problem to face. Drug Alcohol Depend. Nichols, DE. Chemistry and structure—activity relationships of psychedelics. Effect of hallucinogens on unconditioned behavior. Rychert, M; Wilkins, C. Implications for law enforcement and penalties. New psychoactive substances as adulterants of controlled drugs. A worrying phenomenon? King, LA. New phenethylamines in Europe. Postmortem detection of 25I-NBOMe \\\\\\\\\\\\\\\[2- 4-iodo-2,5-dimethoxyphenyl - N -\\\\\\\\\\\\\\\[ 2-methoxyphenyl methyl\\\\\\\\\\\\\\\]ethanamine\\\\\\\\\\\\\\\] in fluids and tissues determined by high performance liquid chromatography with tandem mass spectrometry from a traumatic death. Structure-activity relationships of serotonin 5-HT 2A agonists. WIREs Membr. Signal , 1 Sep , 1 5 , Identification of 4-substituted 2- 4- x -2,5-dimethoxyphenyl - N -\\\\\\\\\\\\\\\[ 2-methoxyphenyl methyl\\\\\\\\\\\\\\\]ethanamine 25X-NBOMe and analogues by gas chromatography—mass spectrometry analysis of heptafluorobutyric anhydride HFBA derivatives. Adamowicz, P; Zuba, D. Discrimination among designer drug isomers by chromatographic and spectrometric methods. Voltammetric signatures of 2,5-dimethoxy- N - 2-methoxybenzyl phenethylamines on boron-doped diamond electrodes: Detection in blotting paper samples. Development of highly potent partial agonists and chiral antagonists as tools for the study of 5-HT 2A -receptor mediated functions. Classical hallucinogens as antidepressants? A review of pharmacodynamics and putative clinical roles. The varieties of the psychedelic experience: A preliminary study of the association between the reported subjective effects and the binding affinity profiles of substituted phenethylamines and tryptamines. Luethi, D; Liechti, ME. Monoamine transporter and receptor interaction profiles in vitro predict reported human doses of novel psychoactive stimulants and psychedelics. Fatal poisonings associated with new psychoactive substances. McCorvy, JD. Mapping the binding site of the 5-HT 2A receptor using mutagenesis and ligand libraries: Insights into the molecular actions of psychedelics. Thesis , Purdue University, 1 Jan N -Benzylated phenylethanamines are highly potent partial agonists at 5-HT 2A receptors. Toxichem Krimtech , 1 Jan , 86 1 , 5— Analytical data of designer drugs of synthetic phenethylamines. JCCL , 1 Dec , 55 , 43— Correlation between the potency of hallucinogens in the mouse head-twitch response assay and their behavioral and subjective effects in other species. Neuropharmacology , 1 May , Population survey data informing the therapeutic potential of classic and novel phenethylamine, tryptamine, and lysergamide psychedelics. Palamar, JJ; Acosta, P. A qualitative descriptive analysis of effects of psychedelic phenethylamines and tryptamines. Quick test for determination of N-bombs Phenethylamine derivatives, NBOMe using high-performance liquid chromatography: A comparison between photodiode array and amperometric detection. ACS Omega , 10 Sep , 4 11 , — Development and validation of a color spot test method for the presumptive detection of NBOMe compounds. To explore a different substance… one of the matching names from the list; e. IUPAC names 2- 4-Iodo-2,5-dimethoxyphenyl - N -\\\\\\\\\\\\\\\[ 2-methoxyphenyl methyl\\\\\\\\\\\\\\\]ethanamine 2- 4-Iodo-2,5-dimethoxyphenyl - N - 2-methoxybenzyl ethanamine.

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