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    AM-694 molecular structure

    AM-694 Stats & Data

    Shamrock Pulse ultra Warrior ultimate
    NPS DataHub
    MW435.28
    FormulaC20H19FINO
    CAS335161-03-0
    IUPAC1-[(5-fluoropentyl)-1H-indol-3-yl]-(2-iodophenyl)methanone
    SMILESFCCCCCN1:C:C(C(=O)c2ccccc2I)c2ccccc12
    Cannabinoids; 2020/2.1 Von Indol Pyrazol und 4-Chinolon abgeleitete Verbindungen; 2021/2.1 Von Indol Pyrazol und 4-Chinolon abgeleitete Verbindungen; 2022/2.1 Von Indol Pyrazol und 4-Chinolon abgeleitete Verbindungen
    Chemical Class Cannabinoid
    Psychoactive Class Depressant / Psychedelic
    Half-Life Animal data suggest plasma t½ ≈ 3–8 h; subjective effects resolve sooner due to redistribution.

    Receptor Profile

    Receptor Actions

    Agonists
    CB1 receptor agonist (full)
    CB2 receptor agonist (full)

    Effect Profile

    Curated
    Psychedelic 4.4

    Moderate body load with mild visuals, headspace, and auditory effects

    Visual Intensity×3
    5
    Headspace Depth×3
    4
    Auditory Effects×1
    4
    Body Load / Somatic Effects×1
    6

    Tolerance & Pharmacokinetics

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    Half-Life
    Animal data suggest plasma t½ ≈ 3–8 h; subjective effects resolve sooner due to redistribution.
    Addiction Potential
    Moderate-to-high. As a full CB1 agonist it produces tolerance rapidly and can cause withdrawal (irritability, insomnia, nausea) after daily use of ≥1 week. Psychological craving comparable to other potent synthetic cannabinoids.

    Legal Status

    Country Status Notes
    Finland AM-694 is scheduled in the "government decree on psychoactive substances banned from the consumer market".

    Harm Reduction

    drugs.wiki

    AM-694 is an extremely potent CB1-preferring agonist originally developed for PET imaging; sub-milligram accuracy is mandatory. Consider volumetric dosing to mitigate measurement error with such potency. Forum-era reports describe a calm, plateauing high in some, but acute anxiety, tachycardia, confusion, and brief psychotic symptoms in others; several reports of short hospitalisations occurred shortly after its appearance in 2010. Severe and unpredictable adverse effects (e.g., agitation, seizures, loss of consciousness, acute kidney injury) are well documented for the synthetic cannabinoid class; AM-694’s safety profile is poorly characterised. Avoid unknown ‘herbal blend’ products and homemade sprays—batch-to-batch variability and mislabeling were common in early markets. Combining with CNS depressants (opioids, alcohol, benzodiazepines, GHB) increases risk of dangerous respiratory/CNS suppression; with stimulants it increases cardiovascular strain and panic risk. Start with very low test doses, wait full onset (especially oral), and avoid redosing loops—rapid tolerance and compulsion to redose are typical with potent synthetics. Prefer controlled vaporisation over direct flame to limit unknown pyrolysis byproducts; do not heat solutions on coils to charring. Reagent kits are generally unreliable for identifying synthetic cannabinoids; only lab-grade analysis can confirm identity/potency. Long-term safety is unknown; avoid frequent use and consider extra caution if you have cardiovascular, seizure, or psychiatric risk factors.

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