2C-T-4

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2C-T-4, also known as 4-isopropylthio-2,5-dimethoxyphenethylamine, is a psychedelic drug of the phenethylamine and 2C families.<ref name="PiHKAL">Template:CitePiHKAL</ref><ref name="ShulginManningDaley2011">Template:Cite book</ref> It is taken orally.<ref name="PiHKAL" />

2C-T-4 was first described in the scientific literature by Alexander Shulgin and colleagues in 1991.<ref name="ShulginShulginJacob1991" /> Shortly after this, Shulgin described 2C-T-17 in greater detail in his 1991 book PiHKAL (Phenethylamines I Have Known and Loved).<ref name="PiHKAL" />

Use and effects

In his book PiHKAL (Phenethylamines I Have Known and Loved), Alexander Shulgin lists 2C-T-4's dose range as 8 to 20Template:Nbspmg orally and its duration as 12 to 18Template:Nbsphours.<ref name="PiHKAL" /> Its onset is 30Template:Nbspminutes to 2Template:Nbsphours and peak effects occur after 3Template:Nbsphours.<ref name="PiHKAL" /> The effects of 2C-T-4 have been described and include psychedelic visuals among others.<ref name="PiHKAL" /> Shulgin devoted a chapter in the first part of PiHKAL to 2C-T-4, describing an intense "plus-four" experience on the Shulgin Rating Scale with a 12Template:Nbspmg dose.<ref name="PiHKAL" />

Interactions

Template:See also

2C drugs are metabolized by the monoamine oxidase (MAO) enzymes MAO-A and MAO-B.<ref name="DeanStellpflugBurnett2013">Template:Cite journal</ref><ref name="TheobaldMaurer2007">Template:Cite journal</ref> Monoamine oxidase inhibitors (MAOIs) such as phenelzine, tranylcypromine, moclobemide, and selegiline may potentiate the effects of 2C drugs.<ref name="DeanStellpflugBurnett2013" /><ref name="TheobaldMaurer2007" /><ref name="HalmanKongSarris2024">Template:Cite journal</ref> This may result in overdose and serious toxicity.<ref name="HalmanKongSarris2024" /><ref name="DeanStellpflugBurnett2013" />

Pharmacology

Pharmacodynamics

Template:Nowrap
Target Affinity (Ki, nM)
5-HT1A 470–916
5-HT1B Template:Abbr
5-HT1D Template:Abbr
5-HT1E Template:Abbr
5-HT1F Template:Abbr
5-HT2A 27.9–54 (Ki)
5.5–220 (Template:Abbrlink)
56–87% (Template:Abbrlink)
5-HT2B Template:Abbr (Ki)
63–160 (Template:Abbr)
68–75% (Template:Abbr)
5-HT2C 180–295 (Ki)
Template:Abbr (Template:Abbr)
Template:Abbr (Template:Abbr)
5-HT3 Template:Abbr
5-HT4 Template:Abbr
5-HT5A Template:Abbr
5-HT6 Template:Abbr
5-HT7 Template:Abbr
α1A 11,000
α1B, α1D Template:Abbr
α2A 130–217
α2B, α2C Template:Abbr
β1β3 Template:Abbr
D1 20,000
D2 16,000
D3 19,000
D4, D5 Template:Abbr
H1 >25,000
H2H4 Template:Abbr
M1M5 Template:Abbr
I1 Template:Abbr
σ1, σ2 Template:Abbr
Template:Abbrlink 2,337–4,500 (Ki) (mouse)
19–53 (Ki) (rat)
3,700 (Template:Abbr) (mouse)
83 (Template:Abbr) (rat)
>30,000 (Template:Abbr) (human)
51% (Template:Abbr) (mouse)
67% (Template:Abbr) (rat)
Template:Abbrlink >30,000 (Ki)
113,000 (Template:Abbrlink)
Template:Abbr (Template:Abbr)
Template:Abbrlink 17,000 (Ki)
134,000 (Template:Abbr)
Template:Abbr (Template:Abbr)
Template:Abbrlink >30,000 (Ki)
294,000 (Template:Abbr)
Template:Abbr (Template:Abbr)
Notes: The smaller the value, the more avidly the drug binds to the site. All proteins are human unless otherwise specified. Refs: <ref name="PDSPKiDatabase">{{#invoke:citation/CS1|citation CitationClass=web

}}</ref><ref name="RickliLuethiReinisch2015">Template:Cite journal</ref><ref name="LuethiTrachselHoener2018">Template:Cite journal</ref><ref name="SimmlerBuchyChaboz2016">Template:Cite journal</ref>

2C-T-4 acts as a serotonin 5-HT2 receptor agonist, including of the serotonin 5-HT2A receptor.<ref name="LuethiTrachselHoener2018" /><ref name="RickliLuethiReinisch2015" /> The mechanism that produces 2C-T-4's hallucinogenic effects has not been specifically established, however it is most likely to result from 5-HT2A receptor activation in the brain, a mechanism of action shared by all of the hallucinogenic tryptamines and phenethylamines for which the mechanism of action is known.

Chemistry

2C-T-4 is the 2-carbon homologue of Aleph-4.<ref name="PiHKAL" /> The full chemical name is 2-[4-(isopropylthio)-2,5-dimethoxyphenyl]-ethanamine.<ref name="PiHKAL" /> The drug has structural and pharmacodynamic properties similar to 2C-T-7 and 2C-T-19.<ref name="PiHKAL" /> A notable analogue of 2C-T-4 is the Ψ-PEA compound Ψ-2C-T-4.<ref name="PiHKAL" />

Synthesis

The chemical synthesis of 2C-T-4 has been described.<ref name="PiHKAL" />

History

2C-T-4 was first described in the scientific literature by Alexander Shulgin and colleagues in a journal article in 1991.<ref name="ShulginShulginJacob1991">Template:Cite journal</ref> Shortly thereafter, it was described in greater detail by Shulgin in his 1991 book PiHKAL (Phenethylamines I Have Known and Loved).<ref name="PiHKAL" />

Society and culture

Canada

As of October 31, 2016, 2C-T-4 is a controlled substance (Schedule III) in Canada.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref>

China

As of October 2015 2C-T-4 is a controlled substance in China.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref>

Denmark

2C-T-4 is added to the list of Schedule B controlled substances.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref>

Sweden

Sveriges riksdags health ministry Statens folkhälsoinstitut classified 2C-T-4 as "health hazard" under the act Lagen om förbud mot vissa hälsofarliga varor (translated Act on the Prohibition of Certain Goods Dangerous to Health) as of Jul 15, 2007, in their regulation SFS 2007:600 listed as 2,5-dimetoxi-4-isopropyltiofenetylamin (2C-T-4), making it illegal to sell or possess.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref>

United States

As of July 9, 2012, 2C-T-4 is a Schedule I substance in the United States, under the Synthetic Drug Abuse Prevention Act of 2012.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref>

See also

References

Template:Reflist

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