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IDNNA (2,5-dimethoxy-4-iodo-N,N-dimethylamphetamine) is a lesser-known psychedelic drug and a substituted amphetamine. It is also the N,N-dimethyl analog of DOI. IDNNA was first synthesized by Alexander Shulgin. In his book PiHKAL, the minimum dosage is listed as 2.6 mg, and the duration unknown. [1] IDNNA produces few to no effects.
Several 5-HT 2A agonist hallucinogens including (R)-2,5-dimethoxy-4-iodoamphetamine DOI, TCB-2, LSD and LA-SS-Az have unexpectedly also been found to act as potent inhibitors of TNF, with DOI being the most active, showing TNF inhibition in the picomolar range, an order of magnitude more potent than its action as a hallucinogen. [6] [7] [8]
The page provides a comprehensive list of isomers of dodecane, including their chemical structures and properties.
The parent isoindole was prepared by flash vacuum pyrolysis of an N-substituted isoindoline. [5] N-Substituted isoindoles, which are easier to handle, can be prepared by dehydration of isoindoline-N-oxides. They also arise by myriad other methods, e.g., starting from xylylene dibromide (C 6 H 4 (CH 2 Br) 2).
2,5-Dimethoxy-4-ethylamphetamine (DOET, DOE, Hecate) is a psychedelic drug of the phenethylamine and amphetamine chemical classes. It was first synthesized by Alexander Shulgin , and was described in his book PiHKAL ( Phenethylamines i Have Known And Loved ).
And they are. That perfect combination of highly coveted items in limited quantities is basically a recipe for success on Instagram, where it has more than 1.3 million posts, along with TikTok and ...
They work by inhibiting the effects of an enzyme known as 5-alpha reductase, which converts testosterone into dihydrotestosterone (DHT), a hormone responsible for male pattern hair loss.
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