Talk:Glaucine

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Summary sheet: Glaucine

Glaucine is a naturally occurring novel psychedelic substance of the aporphine class found in Glaucium Flavum.[1] Glaucine has one stereocenter, therefore it has two stereoisomers, where (S)-Glaucine is a 5-HT2A agonist and (R)-Glaucine is a 5-HT2 positive allosteric modulator.[2] Its psychedelic effects are believed to be produced by its interaction with serotonin receptors like most psychedelics do, but also has clinically significant interactions at D1,[3] α1, and benzothiazepine receptors as an antagonist, and inhibits MOA to a moderate degree.[4] Glaucine has a close relative found in Blue Lotus (Nymphaea nouchali) called apomorphine. It is both psychedelic as well as sedating, but the sedation is more similar to that of opioids than psilocybin, a generally sedating psychedelic. It is most commonly consumed orally.

Glaucine is rarely sold on the streets and almost exclusively distributed as a legal alternative to more common psychedelics, where it is commonly used for recreational and entheogenic purposes. It was and still is a very uncommon and unheard of substance with sparing experiences on the internet.

Due to its potent sedating effects as well as unknown toxicity profile, it is strongly recommended that one use proper harm reduction practices if choosing to use this substance.

Glaucine
Chemical Nomenclature
Common names DMT, Dimethyltryptamine, Dmitri
Substitutive name N,N-Dimethyltryptamine
Systematic name 2-(1H-Indol-3-yl)-N,N-dimethylethanamine
Class Membership
Psychoactive class Psychedelic
Chemical class Tryptamine
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
Bioavailability x% - y%[5]
Threshold x - mg
Light x - y mg
Common x - y mg
Strong x - y mg
Heavy x mg +
Duration
Total x - y hours
Onset x - y minutes
Come up x - y minutes
Peak x - y hours
Offset x - y hours
After effects x - y hours


Sublingual
Dosage
Bioavailability x% - y%
Threshold x - mg
Light x - y mg
Common x - y mg
Strong x - y mg
Heavy x mg +
Duration
Total a - b hours
Onset a - b minutes
Come up a - b minutes
Peak a - b hours
Offset a - b hours
After effects a - b 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.


History and culture

Glaucine was first described in 1839 by Probst, defined as an 'acrid alkaloid, and was first isolated by Richard Fischer in 1901.[6] It has been used used for millennia, where records back to the year 131 claim it was used for aches and sores as well as abscess' in present-day Turkey.[6] In an overview study in 2007, glaucine's antitussive effectiveness was confirmed along with its potent bronchodilation effects, but lacked the respiratory depression and habit-forming use associated with opioid antitussives.[7] Today, it is sold as an antitussive medicine in Iceland and eastern European countries, as well as being used off-label for asthma.[8]

 

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Chemistry

Glaucine is an aporphine, meaning 'not morphine.' It is named this because despite similar structure to morphine, it is in fact not morphine. Aporphine is the parent compound of glaucine, where glaucine has methoxy groups substituted at the 1, 2, 9, and 10 positions. Glaucine has one stereocenter, meaning it has two stereoisomers. Both stereoisomers are found in nature, albeit in different plants.[9]

 

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Pharmacology

Glaucine is a sedative-psychedelic. The psychedelic effects perceived from glaucine are in fact from interaction of 5-HT2A receptors, but both stereoisomers of glaucine interact with the receptor differently. (S)-glaucine is an agonist of the receptor, the same action performed by psychedelics like LSD and mescaline, but (R)-glaucine is a positive allosteric modulator, meaning it boosts the signaling and activity at the receptor.

 

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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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Disclaimer: The effects listed below cite the Subjective Effect Index (SEI), an open research literature based on anecdotal user reports and the personal analyses of PsychonautWiki contributors. As a result, they should be viewed with a healthy degree of skepticism.

It is also worth noting that these effects will not necessarily occur in a predictable or reliable manner, although higher doses are more liable to induce the full spectrum of effects. Likewise, adverse effects become increasingly likely with higher doses and may include addiction, severe injury, or death ☠.

Physical effects
 

Visual effects
 

Cognitive effects
 

Auditory effects
 

Multi-sensory effects
 

Transpersonal effects
 

Experience reports

There are currently 0 experience reports which describe the effects of this substance in our experience index.

Additional experience reports can be found here:

Toxicity and harm potential

 

This toxicity and harm potential section is a stub.

As a result, it may contain incomplete or even dangerously wrong information! You can help by expanding upon or correcting it.
Note: Always conduct independent research and use harm reduction practices if using this substance.

It is strongly recommended that one use harm reduction practices when using this substance.

Lethal dosage

Tolerance and addiction potential

Dangerous interactions

 

This dangerous interactions section is a stub.

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Warning: Many psychoactive substances that are reasonably safe to use on their own can suddenly become dangerous and even life-threatening when combined with certain other substances. The following list provides some known dangerous interactions (although it is not guaranteed to include all of them).

Always conduct independent research (e.g. Google, DuckDuckGo, PubMed) to ensure that a combination of two or more substances is safe to consume. Some of the listed interactions have been sourced from TripSit.

 

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See also

(List along order below)

Literature

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References

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