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Dimethoxytrityl, often abbreviated DMT, is a protecting group widely used for protection of the 5'-hydroxy group in nucleosides, particularly in oligonucleotide synthesis. [ 1 ] It is usually bound to a molecule, but can exist as a stable cation in solution, where it appears bright orange.
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 .
There are three main methods for the preparation of nucleoside phosphoramidites. DMT = 4,4'-dimethoxytrityl; B = optionally protected nucleic base; R = phosphate protecting group The common method involves treatment of a protected nucleoside bearing a single free hydroxy group with phosphorodiamidite under the catalytic action of a weak acid.
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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 ...
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