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Buy 25B-NBOMe 1g (25B-NBOMe (NBOMe-2C-B, BOM 2-CB, Cimbi-36) is a derivative of the phenethylamine hallucinogen 2C-B, discovered in 2004 by Ralf Heim at the Free University of Berlin. It acts as a potent partial agonist for the 5HT2A receptor. Anecdotal reports from human users suggest 25B-NBOMe to be an active hallucinogen at a dose of as little as 400-650mcg insufflated,
Buy RTI 1g 99% purity. Best trusted resaler online, RTI-126, ((-)-2?-(1,2,4-oxadiazol-5-methyl)-3?-phenyltropane) acts as a potent monoamine reuptake inhibitor and stimulant drug. It is around 5x more potent a stimulant than cocaine, but is relatively unselective, binding to all three monoamine transporters although still with some selectivity for the dopamine transporter. RTI-126 has a fast onset of effects and short duration of action,
Buy indanylaminopropane (IAP) 1g 99.5% purity.an entactogen and psychedelic drug of the amphetamine family.5-APDI acts as a potent and weakly selective serotonin releasing agent (SSRA) with IC50 values of 82 nM, 1,848 nM, and 849 nM for inhibiting the reuptake of serotonin, dopamine, and norepinephrine, respectively
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2C-C-NBOMe (NBOMe-2C-C, 25C-NBOMe) is a derivative of the phenethylamine hallucinogen 2C-C, which acts as a potent partial agonist for the 5HT2A receptor, and has been studied in its 11C radiolabelled form as a potential ligand for mapping the distribution of 5-HT2A receptors in the brain, using positron emission tomography (PET). Anecdotal reports from human users suggest 2C-C-NBOMe to be an active hallucinogen at a dose of as little as 200-500mcg insufflated, making it only slightly less potent than LSD.
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2-Ethoxymethyl salvinorin B (symmetry, 2-EtOMe-Sal B) is a semi-synthetic analogue of the natural product salvinorin A, with a longer duration of action of around 3 hours 99.9% purity.
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98.4% purity. (Jimscaline) Jimscaline (C-(4,5,6-trimethoxyindan-1-yl)methanamine) is a conformationally-restricted derivative of the cactus-derived hallucinogen mescaline, which was discovered in 2006 by a team at Purdue University led by David E. Nichols. It acts as a potent agonist for the 5-HT2A and 5-HT2C receptors with the more active (R)-enantiomer having a Ki of 69nM at the human 5-HT2A receptor, and around three times the potency of mescaline in drug-substitution experiments in animals
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