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N,N-Dimethyltryptamine (DMT or N,N-DMT) is a substituted tryptamine that occurs in many plants and animals, including humans, and which is both a derivative and a structural analog of tryptamine. [1] [2] [3] DMT is used as a psychedelic drug and prepared by various cultures for ritual purposes as an entheogen. [9]
Pharmaceutical compound Poppers A selection of over-the-counter poppers on display Clinical data Other names popper, poppe Routes of administration Inhalation Drug class Vasodilator Legal status Legal status AU: S4 (Prescription only) in general; some exceptions Elsewhere, usually available OTC Pharmacokinetic data Bioavailability When inhaled, Amyl nitrite: unknown Isopropyl nitrite: 43% ...
The LSD is taken first, followed by the MDMA 4 hours later and then 2C-B is taken 2 hours after the MDMA ( so 6 hours after the LSD ). MDMA can be replaced by 6-APB, 5-APB, 6-MAPB or 5-MAPB, in this case the Empathogen is taken 2 hours after the LSD, while 2C-B may be replaced by 2C-C, 2C-D or 2C-B-FLY.
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6-MeO-DMT, or 6-methoxy-N,N-dimethyltryptamine, also known as 6-OMe-DMT, is a serotonergic drug of the tryptamine family. [ 1 ] [ 2 ] It is the 6- methoxy derivative of the serotonergic psychedelic N , N -dimethyltryptamine (DMT) and is a positional isomer of the serotonergic psychedelic 5-MeO-DMT .
5-MeO-DMT is lipophilic and is thought to easily cross the blood–brain barrier. [2] Accordingly, 5-MeO-DMT readily accumulates in the brain in animals with levels higher than in blood. [2] This is in notable contrast to bufotenin (5-HO-DMT or N,N-dimethylserotonin) and serotonin (5-HT), which are hydrophilic and peripherally selective. [2 ...
It is the α,N-dimethyl positional isomer of N,N-dimethyltryptamine (N,N-DMT). [1] α,N-DMT was first synthesized by Alexander Shulgin. [1] In his book TiHKAL (Tryptamines I Have Known and Loved), Shulgin lists the route as oral, the dosage as 50 to 100 mg, and the duration as 6 to 8 hours. [1]