Myristicin

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Myristicin is a phenylpropene, a natural organic compound which is classed as a deliriant, present in small amounts in the essential oil of nutmeg and to a lesser extent in other spices such as parsley and dill.[1] It is believed that Myristicin, along with elemicin and safrole, are the main psychoactive components found within nutmeg, responsible for it's psychoactive properties.

Myristicin
Chemical Nomenclature
Common names Nutmeg
Substitutive name Myristicin, 3-methoxy,4,5-methylenedioxy-allylbenzene
Systematic name 6-allyl-4-methoxy-1,3-benzodioxole
Class Membership
Psychoactive class Deliriant
Chemical class Phenylpropene / MDxx
Routes of Administration

WARNING: Always start with lower doses due to differences between individual body weight, tolerance, metabolism, and personal sensitivity. See responsible use section.



Oral
Dosage
Light 50 - 200 mg
Common 200 - 500 mg
Strong 500 - 800 mg
Heavy 800 mg +
Duration
Total 12 - 72 hours
Onset 3 - 8 hours
Come up 1 - 4 hours
Peak 9 - 12 hours
Offset 12 - 48 hours
After effects 24 - 72 hours









DISCLAIMER: PW's dosage information is gathered from users and resources for educational purposes only. It is not a recommendation and should be verified with other sources for accuracy.

Interactions
Benzodiazepines
Depressants
Stimulants
Alcohol
Serotonin releasers
Opioids
DXM
DPH
Summary sheet: Myristicin

Myristicin acts as an anticholinergic, and is the traditional precursor for the psychedelic and empathogenic drug MMDA.

Nutmeg was reported to induce hallucinogenic effects, such as visual distortions and paranoid ideation. In the reports, nutmeg intoxication took several hours before maximum effect was reached. Effects and after-effects lasted up to several days. Raw nutmeg consists of 5-15% essential oil by mass. 4-8.5% of nutmeg essential oil, or 0.2-1.3% of raw nutmeg, is myristicin. One study found 20 grams of nutmeg to contain 210 mg myristicin.[2]

Chemistry

 

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Myristicin belongs to a chemical class known as phenylpropene. It features a methylenedioxy ring at the R4 and R5 positions, as well as a separate methoxy group at the R3 position, fused to the main phenylpropene group.

The phenylpropene group consists of an allyl group attached to a benzene ring.

Pharmacology

 

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In 1963, Alexander Shulgin speculated myristicin could be metabolized to MMDA, a psychoactive drug related to MDA, in the liver.[3] This, however, is highly speculative. Myristicin is also found to be a serotonin receptor antagonist, while simultaneously acting as a weak MAO inhibitor.

Subjective effects

 
This subjective effects section is a stub.

As such, it is still in progress and may contain incomplete or wrong information.

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The effects listed below are based upon the subjective effects index and personal experiences of PsychonautWiki contributors. The listed effects will rarely (if ever) occur all at once, but heavier dosages will increase the chances and are more likely to induce a full range of effects.

In comparison to datura or diphenhydramine, it's effects tend to be milder and, depending on the dosage, even be considered pleasant and euphoric. It has unique effects compared to other deliriants or hallucinogens. It also has a long, smooth and enjoyable come-up, where the effects build in a similar manner to cannabis.

Physical effects

The physical effects of myristicin are usually described as mild and tolerable, which makes them different from other deliriants. They can be uncomfortable or pleasurable, depending on the dosage. These are described below and generally include:

Cognitive effects

The cognitive effects of myristicin are described by many as mildly euphoric, but can also be dysphoric throughout the trip, primarily consisting of moderate paranoia. It can also be confusing and disorienting. Myristicin contains unique cognitive effects found almost exclusively in the deliriant class.

The most prominent of these effects include:

Visual effects

Myristicin does not enhance visual stimuli in the way that psychedelics do; instead, it tends to degrade and decrease visual aptitude while increasing hallucinations. These components are detailed below:

Suppression

Hallucinatory states

Myristicin is moderately efficient at inducing delirious hallucinations which can be broken into the categories described below:

Auditory effects

Natural plant sources

Myristicin is found in nutmeg, nutmeg essential oil and to a lesser extent in parsley, dill and other plants.

Dosage:

  • Light: 5 - 20g
  • Common: 20 - 60g
  • Strong: 60 - 100g
  • Heavy: 100g+

Toxicity and harm potential

Myristicin is neurotoxic and can be fatal in extremely high doses.

Myristicin and nutmeg is unscheduled in the US and can be bought in form of either spice, essential oil or as whole nuts.

Experience reports

Anecdotal reports which describe this compound within our experience index include:

Additional experience reports can be found here:

See also

References