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Sveriges riksdag added TMA-2 to schedule I ("substances, plant materials and fungi which normally do not have medical use") as narcotics in Sweden as of Dec 30, 1999, published by Medical Products Agency in their regulation LVFS 2004:3 listed as 2,4,5-trimetoxiamfetamin (TMA-2).
Tebbe's reagent, which is used for the methylenation of esters and ketones, is prepared from TMA and titanocene dichloride. [9] In combination with 20 to 100 mol % Cp 2 ZrCl 2 (zirconocene dichloride), the (CH 3) 2 Al-CH 3 adds "across" alkynes to give vinyl aluminium species that are useful in organic synthesis in a reaction known as ...
An assortment of several designer drugs. Designer drugs are structural or functional analogues of controlled substances that are designed to mimic the pharmacological effects of the parent drug while avoiding detection or classification as illegal.
TMA-2 may be: TMA-2 mine; Soyuz TMA-2, a Russian space exploration mission; 2,4,5-trimethoxyamphetamine, a hallucinogenic drug;
The mechanism that produces the hallucinogenic and entheogenic effects of 2C-TFM is most likely to result from action as a 5-HT 2A serotonin receptor agonist in the brain, a mechanism of action shared by all of the hallucinogenic tryptamines and phenethylamines. 2C-TFM displaced radiolabelled ketanserin from 5-HT 2A/C receptors with a K i of 74.5 nM, as compared to a K i of 80.9 nM for the ...
2,5-Dimethoxy-4-iodoamphetamine (DOI) is a psychedelic drug and a substituted amphetamine. Unlike many other substituted amphetamines, however, it is not primarily a stimulant . [ 3 ] DOI has a stereocenter and R -(−)-DOI is the more active stereoisomer .
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The full name of the chemical is 2,5-dimethoxy-4-bromoamphetamine. DOB has a stereocenter and R -(−)-DOB is the eutomer . This is an important finding as it is suggestive that it is targeting different receptors relative to most other phenethylamines (e.g. MDMA ) where the R -isomer serves as the distomer .