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    PRE-084 molecular structure

    PRE-084 Stats & Data

    Fenclimorate
    NPS DataHub
    MW353.89
    FormulaC19H28ClNO3
    CAS138847-85-5
    IUPAC2-Morpholin-4-ylethyl 1-phenylcyclohexane-1-carboxylate;hydrochloride
    SMILES[Cl-].O=C(OCCN1CCOCC1)C1(CCCCC1)c1ccccc1.[H+]
    InChIKeyQUJWFJNHTBKCLU-UHFFFAOYSA-N
    Others
    Half-Life ~3.3 h in mice (i.v.); human half-life unknown.

    Receptor Profile

    Receptor Actions

    Agonists
    Sigma-1 receptor agonist

    Tolerance & Pharmacokinetics

    drugs.wiki
    Half-Life
    ~3.3 h in mice (i.v.); human half-life unknown.
    Addiction Potential
    Very low; minimal reinforcing properties noted in animals and sparse human anecdotes do not describe compulsive redosing.

    Tolerance Decay

    Full tolerance 7d Half tolerance 14d Baseline ~28d

    No controlled human data on tolerance. Anecdotal users report little acute tachyphylaxis but possible subtle blunting with daily use over >1 week; spacing use by 1–2 weeks likely minimizes carryover. Data quality: anecdotal/low.

    Harm Reduction

    drugs.wiki

    Name hygiene: no credible primary sources link PRE-084 to the alias “Fenclimorate”; retaining that name risks misidentification during procurement or verification. PubChem lists PRE-084 under the cyclohexanecarboxylate/morpholine ester names noted above. PRE-084 is a selective σ1 receptor agonist used as a research ligand; rodent work shows rapid CNS penetration and a plasma half-life near 3.3 h, but human pharmacokinetics remain unknown. σ1 receptor agonism modulates monoaminergic and glutamatergic signaling and can change the behavioural/toxic profile of stimulants; σ1 antagonists (BD1018/BD1063) attenuate several cocaine effects in mice, implying that σ1 agonists could do the opposite. Several SSRIs interact with σ1 (fluvoxamine/fluoxetine/escitalopram as agonists; sertraline with antagonist/inverse agonist properties), making co-use effects unpredictable. Dextromethorphan is itself a σ1 agonist and can interact at σ1 in animal models; combining high-dose DXM with PRE-084 may magnify or alter effects in either direction. Sparse human reports suggest mild mental stimulation, clarity, and occasionally insomnia; schedule daytime trials and avoid late dosing. Because identity/purity vary by vendor, weigh doses on a 0.001 g scale, and adjust for salt form (HCl ≈10–12% heavier than freebase for equivalent molar dose). Avoid inhalation/vaping routes—thermal decomposition profile is unknown for this ester; insufflation can be irritating and may increase bioavailability unpredictably. People with a history of seizures should avoid σ1 agonist stacks; some σ1-active agents (e.g., opipramol) showed proconvulsant effects in a PTZ-kindling mouse model. As a research chemical without established therapeutic window in humans, employ allergy test dosing (e.g., ≤1 mg) and increase only after ≥24 h with no adverse effects. Polysubstance ‘potentiation’ experiments (e.g., with psychedelics or dissociatives) carry poorly characterized risks due to σ1’s broad cellular roles—avoid until single-agent response is well understood.

    References

    Data Sources

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