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4-MeO-PCMo isn’t a popular research chemical, likely because of its relatively low potency compared to other members of the arylcyclohexylamine family. 4′-MeO-PCMo.
The qualitative effects of this drug are not well defined, and there aren’t many good trip reports available for this drug online.
Preliminary testing suggests the Ki receptor binding affinity of this drug is around 2118 nM for the NMDA receptors (low activity) and negligible for the dopamine, serotonin, and norepinephrine transporters. Buy 4′-MeO-PCMo
4-MeO-PCMo isn’t a popular research chemical, likely because of its relatively low potency compared to other members of the arylcyclohexylamine family.
The qualitative effects of this drug are not well defined, and there aren’t many good trip reports available for this drug online.
Preliminary testing suggests the Ki receptor binding affinity of this drug is around 2118 nM for the NMDA receptors (low activity) and negligible for the dopamine, serotonin, and norepinephrine transporters.
4-MeO-PCMo Specs:
| Chemical Name | 4-methoxy-phenylcyclohexyl-morpholine |
| Status | Research Chemical 🧪 |
| Duration of Effects | Unknown |
| Estimated Threshold Dose | Unknown |
| Common Dose | Unknown |
| PubChem ID | 137332210 |
| CAS# | 2201-35-6 |
How Do Arylcyclohexylamines Work?
Arylcyclohexylamines interfere with the function of glutamate — a key neurotransmitter involved with brain function (and, therefore, consciousness). This results in a powerful dissociation of the mind from the body — all without extinguishing consciousness. 4′-MeO-PCMo.
Most of the arylcyclohexylamine class of drugs work by binding to the PCP binding site of the NMDA receptor [8]. PCP was the first compound ever studied and was instrumental in understanding the NMDA receptors. However, most members of this group — not just PCP — bind to this same receptor. Where to buy 4′-MeO-PCMo. Magic mushrooms online store
Once bound, arylcyclohexylamines block the effects of NMDA, resulting in their characteristic dissociative effects. Order 4′-MeO-PCMo
Arylcyclohexylamines also interact with the dopamine transporter (DAT), norepinephrine transporter (NET), and serotonin transporter (SERT) to exert additional effects on mood and cognition. 4′-MeO-PCMo powder.
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For example, PCP is a strong stimulant in addition to its dissociative qualities. This effect stems from the compound’s affinity for dopamine, norepinephrine, and serotonin transporters. By blocking the reuptake of these neurotransmitters, these compounds exert a potent amphetamine-like effect — boosting cognition, increasing vigilance and alertness, and raising body temperature.
One study found PCP was 8 times more potent than D-amphetamine and 34 times more potent than methylphenidate at inhibiting serotonin (5-HT) uptake [12].
Several psychoactive drugs have been found to interact with these receptors in addition to PCP and PCP-analogs. Including cocaine, morphine, fluvoxamine, methamphetamine, and DXM (dextromethorphan). 4′-MeO-PCMo for sale.
The binding affinity for each arylcyclohexylamine varies — some have a stronger dopamine component; others are stronger NMDA antagonists. These changes in binding affinity impact the drugs’ subjective effect profile. Making them stronger dissociatives, sedatives, or stimulants than other members of the group. Pennsylvania mushroom shop
The arylcyclohexylamine class is also notoriously biphasic in terms of their effects. This means they produce different effects in low doses than they do in higher doses. In general, lower doses are stimulating, while higher doses are sedative and cataleptic. Most members of this group share these qualities.
List of Primary Target Receptors for the Arylcyclohexylamine Class:
| Receptor | Interaction | Effect Outcome |
| N-Methyl-D-Aspartate (NMDA) Receptors | Antagonistic (Inhibits) | Dissociation, sedation, neuroprotective (dose-dependant), |
| Opioid Receptors | Agonistic (Stimulates) | Analgesia, sedation, euphoria, anxiolysis |
| Dopamine (D2) Receptors | Agonistic (Stimulates) | Hallucinations, euphoria, mental & physical stimulation, thermogenesis |
| Dopamine Transporters (DAT) | Antagonist (Inhibits) | Stimulation, hallucinations, euphoria, thermogenesis |
| Norepinephrine Transporters (NET) | Antagonist (Inhibits) | Stimulation, thermogenesis |
| Serotonin Transporters (SERT) | Antagonist (Inhibits) | Euphoria, hallucinations |
| Sigma Receptors | Agonistic (Stimulates) | Hallucinations, dissociation |
| Nicotinic Acetylcholine (nACh) Receptors | Antagonistic (Inhibits) | Muscle-relaxation, intoxication |





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