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Dimethyltryptamine

Dimethyltryptamine
History[edit] Another historical milestone is the discovery of DMT in plants frequently used by Amazonian natives as additive to the vine Banisteriopsis caapi to make ayahuasca decoctions. Biosynthesis[edit] Biosynthetic pathway for N,N-dimethyltryptamine This transmethylation mechanism has been repeatedly and consistently proven by radiolabeling of SAM methyl group with carbon-14 (14C-CH3)SAM).[22][20][24][25][26] Evidence in mammals[edit] In 2013, researchers first reported DMT in the pineal gland microdialysate of rodents.[28] A study published in 2014 reported the biosynthesis of N,N-dimethyltryptamine (DMT) in the human melanoma cell line SK-Mel-147 including details on its metabolism by peroxidases. [29] In a 2014 paper, a group first demonstrated the immunomodulatory potential of DMT and 5-MeO-DMT through the Sigma-1_receptor of human immune cells. INMT[edit] Endogenous DMT[edit] The first claimed detection of mammalian endogenous DMT was published in June 1965: German researchers F. Related:  Pineal Gland (Bull.S. New Age Meditation)

Entheogen A group of peyotes, in cultivation. 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. Etymology[edit] The neologism entheogen was coined in 1979 by a group of ethnobotanists and scholars of mythology (Carl A. Entheogen was coined as a replacement for the terms hallucinogen and psychedelic. Ruck et al. argued that the term hallucinogen was inappropriate owing to its etymological relationship to words relating to delirium and insanity. In a strict sense, only those vision-producing drugs that can be shown to have figured in shamanic or religious rites would be designated entheogens, but in a looser sense, the term could also be applied to other drugs, both natural and artificial, that induce alterations of consciousness similar to those documented for ritual ingestion of traditional entheogens. Entheogens[edit] Species[edit]

Salvinorin A Salvinorin A is the main active psychotropic molecule in Salvia divinorum, a Mexican plant which has a long history of use as an entheogen by indigenous Mazatec shamans. Salvinorin A is considered a dissociative exhibiting atypically psychedelic effects. Salvinorin A can produce psychoactive experiences in humans with a typical duration of action being several minutes to an hour or so, depending on the method of ingestion.[2] History[edit] Salvinorin A was first described and named in 1982 by Alfredo Ortega and colleagues in Mexico. Pharmacology[edit] Potency and selectivity[edit] Salvinorin A is unique in that it is the only naturally occurring substance known to induce a visionary state via this mode of action; there are synthetic kappa-opioid agonists, (e.g. enadoline, ketazocine, pentazocine and relatives), which show similar hallucinatory and dissociative effects. Effect on intestinal motility[edit] Solubility[edit] Detection in urine[edit] Associated compounds[edit] Synthesis[edit]

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. 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] Tetrahydrocannabinol with double bond isomers and their stereoisomers is one of only three cannabinoids scheduled by Convention on Psychotropic Substances (the other two are dimethylheptylpyran and parahexyl). Pharmacology[edit]

Library : The Erowid Review » Sex, Drugs, Einstein & Elves: Sushi, Psychedelics, Parallel Universes, and the Quest for Transcendence Sex, Drugs, Einstein & Elves: Sushi, Psychedelics, Parallel Universes, and the Quest for Transcendence by Clifford Pickover Publisher: Smart Publications Clifford Pickover has a lot of energy. Across eleven chapters, Pickover cuts a wide swath with his literary machete, hacking through such subjects as language, DMT, machine elves, Terence McKenna, his hometown in upstate New York, book publishing, the virus theory of language, Einstein, God, transcendence, the Big Crunch, and, oh yeah, Burning Man.

Endocrine system In addition to the specialised endocrine organs mentioned above, many other organs that are part of other body systems, such as bone, kidney, liver, heart and gonads, have secondary endocrine functions. For example the kidney secretes endocrine hormones such as erythropoietin and renin. A number of glands that signal each other in sequence are usually referred to as an axis, for example, the hypothalamic-pituitary-adrenal axis. As opposed to endocrine factors that travel considerably longer distances via the circulatory system, other signaling molecules, such as paracrine factors involved in paracrine signalling diffuse over a relatively short distance. The word endocrine derives from the Greek words ἐνδο- endo- "inside, within," and κρίνειν krinein "to separate, distinguish". Endocrine organs and known secreted hormones[edit] Endocrine glands in the human head and neck and their hormones Hypothalamus[edit] Pineal body (epiphysis)[edit] Pituitary gland (hypophysis)[edit] Thyroid[edit] Skin[edit]

Ibogaine Ibogaine is a naturally occurring psychoactive substance found in plants in the Apocynaceae family such as Tabernanthe iboga, Voacanga africana and Tabernaemontana undulata. A psychedelic with dissociative properties, the substance is banned in some countries; in other countries it is used by proponents of psychedelic therapy to treat addiction to methadone, heroin, alcohol, cocaine, methamphetamine, anabolic steroids, and other drugs. Ibogaine is also used to treat depression and post traumatic stress disorder. Ibogaine-containing preparations are used for medicinal and ritual purposes within African spiritual traditions of the Bwiti, who claim to have learned it from the Pygmy peoples. Ibogaine is an indole alkaloid that is obtained either by extraction from the iboga plant or by semi-synthesis from the precursor compound voacangine,[3][4] another plant alkaloid. History[edit] An ibogaine research project was funded by the US National Institute on Drug Abuse in the 1990s.

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. 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] Modern[edit] Albert Hofmann (shown here in 1993) purified psilocybin and psilocin from Psilocybe mexicana in the late 1950s. Occurrence[edit]

postmarketOS: An Ultimate Linux Distro For Your Smartphones Is Coming One of the key strengths of Linux-based operating systems is their ability to run on a variety of hardware, ranging from a decade old computers to the latest generation Intel chips. The kernel developers work day and night to keep our devices breathing running. In the past, we have also prepared a list of Linux distributions that are best suited for older computers with limited hardware requirements. This brings us to the question — Why aren’t tons of Linux operating system options available for mobile devices? What is postmarketOS? postmarketOS is based on Alpine Linux distro, which is a security-oriented and lightweight Linux distro. postmarketOS, being developed by Oliver Smith, doesn’t intend to restrict users to one user interface. We are all are aware of the fact the Android struggles with the update process as the OEMs need to fork the entire codebase for each Android device and version. Did you find the concept of postmarketOS Linux distro for smartphones interesting?

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