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Little is known about the subjective effects of 5-MeO-DPT, but the nature of the compound is probably comparable to 5-MeO-DiPT, 5-MeO-DMT, or DPT, which are also psychedelic tryptamines/indoles. However, the duration of the above-mentioned drugs vary considerably.
5-MeO-isoDMT, or 5-OMe-isoDMT, also known as 5-methoxy-N,N-dimethylisotryptamine, is a putatively non-hallucinogenic serotonin 5-HT 2A receptor agonist and psychoplastogen of the isotryptamine group.
5-MeO-α-ET produces entactogenic and stimulant effects that can last 4–6 hours. However, little information exists on the psychopharmacological effects of this compound, thus considerable variation with regard to dosage and effects can be expected.
5-Methoxy-2,N,N-trimethyltryptamine (5-MeO-2,N,N-TMT, 5-MeO-TMT) is a psychoactive drug of the tryptamine chemical class which acts as a psychedelic.It was first synthesized by Alexander Shulgin and reported in his book TiHKAL ("Tryptamines i Have Known And Loved").
5,N-Dimethyl-N-isopropyltryptamine (5-Me-MiPT) is a tryptamine derivative that is thought to be a psychedelic drug.It was first made in 1989. In vitro binding experiments on brain homogenates showed it to have serotonin receptor binding affinity between that of MiPT and 5-MeO-MiPT, [1] both of which are known to be active psychedelics in humans.
5-MeO-MET (5-Methoxy-N-methyl-N-ethyltryptamine) is a relatively rare designer drug from the substituted tryptamine family, related to compounds such as N-methyl-N-ethyltryptamine and 5-MeO-DMT. [ 1 ] [ 2 ] [ 3 ] It was first synthesised in the 1960s and was studied to a limited extent, [ 4 ] [ 5 ] but was first identified on the illicit market ...
5-MeO-DiBF is a psychedelic [1] that has been sold online as a designer drug and was first definitively identified in December 2015 by a forensic laboratory in Slovenia. [2] It is thought to act as an agonist for the 5-HT 1A and 5-HT 2 family of serotonin receptors .
Like many other psychedelics, aleph is a partial agonist at the 5-HT 2A receptor (EC 50 = 10 nM). [2] It has weak MAO-A inhibitory activity with an IC 50 of 5.2 μM. For reference, amphetamine has an IC 50 of 11 μM and 4-methylthioamphetamine has a value of 0.2 μM. [ 3 ]