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3-MeO-PCP, Angel Dust

Chemical Names: 3-Methoxyphencyclidine

Molecular Formula: C18H27NO

Molecular Weight: 273.42 g·mol−1

IUPAC Name: 1-[1-(3-methoxyphenyl)cyclohexyl]-piperidine

 

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Product Description

Buy 3-meo-pcp Powder Research Chemical Online

Buy 3-MeO-PCE Methoxyeticyclidine Online, 3-MeO-PCP (3-Methoxyphencyclidine) is a potent Dissociative chemical of the Arylcyclohexylamine class.

This chemical was first synthesize in the late 1970s but was not widely report until the later 90s. 3-MeO-PCP is also a derivative of PCP (Phencyclidine).

3-Meo-PCP has been available on the Research Chemical market since 2009 and Researchers of this chemical have state similar results.

to that of other Dissociatives such as MXE and 3-MeO-PCE in their experiments.

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However, compared to other Dissociatives, the chemical is said to be more stimulating and less immobilizing. This chemical works by blocking the NMDA receptors in the brain.   *Disclaimer: Our products are NOT design for human consumption but research purposes ONLY. Adequate safety precautions should be take when researching these chemicals.* 3-MeO-PCP is a Ki of 20 nM for the dizocilpine (MK-801) site of the NMDA receptor, 216 nM for the serotonin transporter (SERT), and 42 nM for the sigma σ1 receptor. It does not bind to the norepinephrine or dopamine transporter nor to the sigma σ2 receptor (Ki >10,000 nM).Base on its structural similarity to 3-hydroxy-PCP (3-HO-PCP). which uniquely among arylcyclohexylamines is high affinity for the μ-opioid receptor in addition to the NMDA receptor, it was initially expect that 3-MeO-PCP would have opioid activity.[1][4] However, radioligand binding assays with human proteins have show that.  contrary to common belief, the drug also does not interact with the μ-, δ-, or κ-opioid receptors at concentrations of up to 10,000 nM.[2] As such, the notion that 3-MeO-PCP has opioid activity has been describe as a myth.[1] 3-MeO-PCP binds to the NMDA receptor with higher affinity than PCP and has the highest affinity of the three isomeric anisyl-substitutions of PCP, followed by 2-MeO-PCP and 4-MeO-P

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3-MeO-PCE

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