3-MeO-PCP

From WikiMD's Wellness Encyclopedia

Error creating thumbnail:
3-MeO-PCP structure

3-MeO-PCP is a dissociative hallucinogen that belongs to the chemical compound class known as arylcyclohexylamines, which also includes phencyclidine (PCP) and ketamine. It acts primarily through antagonism of the NMDA receptor, a type of glutamate receptor in the brain, which plays a key role in neuroplasticity, learning, and memory. Due to its potent effects and potential for misuse, 3-MeO-PCP is of significant interest within both the scientific community and among recreational users.

Chemistry[edit | edit source]

3-MeO-PCP is a derivative of PCP and shares a similar chemical structure with other arylcyclohexylamines. Its full chemical name is 1-(3-methoxyphenyl)cyclohexyl-piperidine, and it possesses the molecular formula C_{18}H_{27}NO. This compound is characterized by a cyclohexane ring bound to a piperidine ring and a methoxy substituted phenyl ring.

Pharmacology[edit | edit source]

The primary mechanism of action of 3-MeO-PCP is antagonism of the NMDA receptor, which inhibits the activity of the glutamate neurotransmitter. Glutamate is the most abundant excitatory neurotransmitter in the vertebrate nervous system, and its receptors are critical for synaptic plasticity, the mechanism underlying learning and memory. By blocking these receptors, 3-MeO-PCP produces dissociative effects, which can range from mild detachment from reality to profound alterations in consciousness.

In addition to its NMDA receptor antagonism, 3-MeO-PCP may interact with other receptor systems, but these interactions are less well understood and require further research to fully elucidate. Its pharmacokinetic properties, such as absorption, distribution, metabolism, and excretion, are also not fully documented in the scientific literature.

Effects[edit | edit source]

The effects of 3-MeO-PCP can vary widely depending on the dose, route of administration, individual physiology, and context of use. Users often report a range of psychological effects, including euphoria, dissociation, altered perception of time and space, and hallucinations. Physical effects can include numbness, increased blood pressure, and impaired motor function. The intensity and duration of these effects can make 3-MeO-PCP particularly hazardous, especially in settings without medical supervision.

Risks and Safety[edit | edit source]

The use of 3-MeO-PCP carries significant risks. Acute adverse effects can include confusion, disorientation, anxiety, and potentially dangerous behavior. There is also a risk of long-term psychiatric and cognitive deficits with repeated use. Due to its potent effects and the variability in individual responses, there is a high potential for accidental overdose, which can be life-threatening.

Legal Status[edit | edit source]

The legal status of 3-MeO-PCP varies by country, with many jurisdictions classifying it as a controlled substance due to its potential for abuse and harm. This classification often makes possession, distribution, and manufacture of 3-MeO-PCP illegal without proper authorization.

Conclusion[edit | edit source]

3-MeO-PCP is a powerful dissociative hallucinogen with significant risks associated with its use. While it has been the subject of scientific research, much remains to be understood about its pharmacology, effects, and safety profile. Individuals considering the use of this substance should be aware of the potential for acute and long-term harm.


This substance-related article is a stub. You can help WikiMD by expanding it.

WikiMD
Navigation: Wellness - Encyclopedia - Health topics - Disease Index‏‎ - Drugs - World Directory - Gray's Anatomy - Keto diet - Recipes

Search WikiMD

Ad.Tired of being Overweight? Try W8MD's physician weight loss program.
Semaglutide (Ozempic / Wegovy and Tirzepatide (Mounjaro / Zepbound) available.
Advertise on WikiMD

WikiMD's Wellness Encyclopedia

Let Food Be Thy Medicine
Medicine Thy Food - Hippocrates

WikiMD is not a substitute for professional medical advice. See full disclaimer.
Credits:Most images are courtesy of Wikimedia commons, and templates Wikipedia, licensed under CC BY SA or similar.

Contributors: Prab R. Tumpati, MD