Neha Patil (Editor)

Harmaline

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Dependence liability
  
N/A

CAS Number
  
304-21-2

ChemSpider
  
10211258

Molar mass
  
214.263 g/mol

Routes of administration
  
Ingestion

PubChem CID
  
5280951

Formula
  
C13H14N2O

Harmaline httpswwwmpbiocomimagesproductimagesmolecu

Legal status
  
AU: S9 (Prohibited) CA: Schedule III

Harmaline a thousand pictures


Harmaline is a fluorescent psychoactive indole alkaloid from the group of harmala alkaloids and beta-carbolines. It is the partially hydrogenated form of harmine.

Contents

Harmaline FileHarmalinesvg Wikimedia Commons

Harmaline


Occurrence in nature

Harmaline Harmaline Wikipedia

Various plants contain harmaline including Peganum harmala (Syrian rue) as well as the hallucinogenic beverage ayahuasca, which is traditionally brewed using Banisteriopsis caapi. Present at 3% by dry weight, the harmala alkaloids may be extracted from the Syrian rue seeds.

Effects

Harmaline FileHarmaline structuresvg Wikimedia Commons

Harmaline is a central nervous system stimulant and a "reversible inhibitor of MAO-A (RIMA)". This means that the risk of a hypertensive crisis, a dangerous high blood pressure crisis from eating tyramine-rich foods such as cheese, is likely lower with harmaline than with irreversible MAOIs such as phenelzine.

Harmaline Erowid Online Books quotTIHKALquot 13 HARMALINE

The harmala alkaloids are psychoactive in humans. Harmaline is shown to act as an acetylcholinesterase inhibitor. Harmaline also stimulates striatal dopamine release in rats at very high dose levels. Since harmaline is a reversible inhibitor of monoamine oxidase A, it could, in theory, induce both serotonin syndrome and hypertensive crises in combination with tyramine, serotonergics, catecholaminergics drugs or prodrugs. Harmaline containing plants and tryptamine containing plants are used in ayahausca brews. The inhibitory effects on monoamine oxidase allows dimethyltryptamine (DMT), the psychologically prominent chemical in the mixture, to bypass the extensive first-pass metabolism it undergoes upon ingestion; allowing a psychologically active quantity of the chemical to exist in the brain for a perceivable period of time. Harmaline forces the anabolic metabolism of serotonin into normelatonin or n-acetylserotonin, and then to melatonin, the body's principle sleep-regulating hormone and a powerful antioxidant.

Harmaline Harmaline C13H14N2O ChemSynthesis

United States Patent Number 5591738 describes a method for treating various chemical dependencies via the administration of harmaline and or other beta-carbolines.

In a study Harmaline has also been found to induce "vasorelaxant effects" in "isolated rat aorta."

A study found that a single injection of 40 mg/kg in rats or 3 x 25 mg/kg spread over 3 days had visible neurotoxic effects.

Harmaline is known to act as a histamine N-methyltransferase inhibitor. This explains how harmaline elicits its wakefulness-promoting effects.

Australia

Harmala alkaloids are considered Schedule 9 prohibited substances under the Poisons Standard (October 2015). A Schedule 9 substance is a substance which may be abused or misused, the manufacture, possession, sale or use of which should be prohibited by law except when required for medical or scientific research, or for analytical, teaching or training purposes with approval of Commonwealth and/or State or Territory Health Authorities.

References

Harmaline Wikipedia