Interesting molecules

Facebook Twitter

Entheogen. A group of peyotes, in cultivation.

Entheogen

Peyote has been used in ritual contexts for thousands of years.[1][2][3] With the advent of organic chemistry, there now exist many synthetic drugs with similar psychoactive properties, many derived from these plants. Psilocybin. Psilocybin[nb 1] (/ˌsɪləˈsaɪbɪn/ SIL-ə-SY-bin) is a naturally occurring psychedelic compound produced by more than 200 species of mushrooms, collectively known as psilocybin mushrooms.

Psilocybin

The most potent are members of the genus Psilocybe, such as P. azurescens, P. semilanceata, and P. cyanescens, but psilocybin has also been isolated from about a dozen other genera. As a prodrug, psilocybin is quickly converted by the body to psilocin, which has mind-altering effects similar (in some aspects) to those of LSD, mescaline, and DMT. In general, the effects include euphoria, visual and mental hallucinations, changes in perception, a distorted sense of time, and spiritual experiences, and can include possible adverse reactions such as nausea and panic attacks.

History[edit] Early[edit] Psilocin. Psilocin (also known as 4-OH-DMT, psilocine, psilocyn, or psilotsin), is a substituted tryptamine alkaloid and a serotonergic psychedelic substance.

Psilocin

It is present in most psychedelic mushrooms together with its phosphorylated counterpart psilocybin. Psilocin is a Schedule I drug under the Convention on Psychotropic Substances.[2] The mind-altering effects of psilocin are highly variable and subjective and resemble those of LSD and DMT. Cannabinoid. Synthetic cannabinoids encompass a variety of distinct chemical classes: the classical cannabinoids structurally related to THC, the nonclassical cannabinoids (cannabimimetics) including the aminoalkylindoles, 1,5-diarylpyrazoles, quinolines, and arylsulphonamides, as well as eicosanoids related to the endocannabinoids.[2] Cannabinoid receptors[edit] Cannabinoid receptor type 1[edit] CB1 receptors are found primarily in the brain, more specifically in the basal ganglia and in the limbic system, including the hippocampus.[1] They are also found in the cerebellum and in both male and female reproductive systems.

Cannabinoid

CB1 receptors are absent in the medulla oblongata, the part of the brain stem responsible for respiratory and cardiovascular functions. Tetrahydrocannabinol. Tetrahydrocannabinol (THC), or more precisely its main isomer (−)-trans-Δ9-tetrahydrocannabinol ( (6aR,10aR)-delta-9-tetrahydrocannabinol), is the principal psychoactive constituent (or cannabinoid) of the cannabis plant.

Tetrahydrocannabinol

First isolated in 1964, in its pure form, by Israeli scientists Raphael Mechoulam and Yechiel Gaoni at the Weizmann Institute of Science,[8][9][10] it is a glassy solid when cold, and becomes viscous and sticky if warmed. A pharmaceutical formulation of (−)-trans-Δ9-tetrahydrocannabinol, known by its INN dronabinol, is available by prescription in the U.S. and Canada under the brand name Marinol. An aromatic terpenoid, THC has a very low solubility in water, but good solubility in most organic solvents, specifically lipids and alcohols.[6] Dimethyltryptamin. Vorlage:Infobox Chemikalie/Summenformelsuche vorhanden N,N-Dimethyltryptamin, kurz DMT, ist ein halluzinogenes Tryptamin-Alkaloid, welches in etlichen Pflanzen, in den Hautdrüsensekreten der Aga-Kröte sowie auch in Spuren im Menschen und in Säugetieren zu finden ist.[8][9][10] Es findet auch Anwendung als Halluzinogen bzw.

Dimethyltryptamin

Entheogen, indem es geraucht (Freibase), geschnupft (als Yopo) oder injiziert (Fumarat) wird.[11] Die perorale Aufnahme (als Ayahuasca) wird nur bei gleichzeitiger bzw. vorheriger Einnahme von Monoaminooxidase-Hemmern (kurz MAOH oder MAOI) erreicht, da DMT sehr rasch (First-Pass-Effekt) vom körpereigenen Enzym Monoaminooxidase abgebaut wird.[11]