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    AMB-CHMICA molecular structure

    AMB-CHMICA Stats & Data

    Mmb-chmica
    NPS DataHub
    MW370.49
    FormulaC22H30N2O3
    CAS1971007-94-9
    IUPACmethyl (2S)-2-[[1-(cyclohexylmethyl)indole-3-carbonyl]amino]-3-methylbutanoate
    SMILESCOC(=O)C(C(C)C)NC(=O)c1cn(CC2CCCCC2)c2ccccc12
    InChIKeyROWZIXRLVUOMCJ-FQEVSTJZSA-N
    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 Psychedelic
    Half-Life Human PK not well defined; casework suggests rapid plasma decline (hours) with metabolites detectable in urine for 1–2 days.

    Effect Profile

    Curated
    Psychedelic 2.6

    Moderate body load with mild visuals, low headspace

    Visual Intensity×3
    5
    Headspace Depth×3
    1
    Auditory Effects×1
    0
    Body Load / Somatic Effects×1
    7

    Tolerance & Pharmacokinetics

    drugs.wiki
    Half-Life
    Human PK not well defined; casework suggests rapid plasma decline (hours) with metabolites detectable in urine for 1–2 days.
    Addiction Potential
    Moderate to high. Daily users report rapid development of tolerance, withdrawal (insomnia, irritability, nausea) and compulsive redosing similar to other potent synthetic cannabinoids.

    Cross-Tolerances

    Other cannabinoid agonists (e.g., THC, other SCRAs)
    50% ●○○

    Harm Reduction

    drugs.wiki

    Naming matters for harm reduction: the substance widely risk‑assessed by EU authorities and linked to multiple deaths is MDMB‑CHMICA (indole tert‑leucinate). ‘AMB‑CHMICA’ is often used online but can refer ambiguously to other analogues; misnaming increases dosing and identification errors. The compound is an extremely potent CB1 full agonist (sub‑nanomolar activity) and has caused clusters of severe poisonings and fatalities in Europe; very small errors can lead to overdose. Herbal blends are notorious for ‘hot spots’—non‑uniform distribution that produces unpredictable overdoses; always avoid eyeballing powders or spraying by guesswork. Routine point‑of‑care urine screens generally do not detect most SCRAs; lack of a positive screen does not imply safety or absence of exposure. Volumetric dosing of accurately weighed material (e.g., in PG/EtOH) and single‑puff test titration with long waits are strongly advised. Red flags requiring urgent care include chest pain, severe agitation/confusion, seizures, syncope, or persistent vomiting. Dependence and severe withdrawal syndromes are well‑described with frequent use; plan long breaks and avoid daily patterns. Avoid combining with CNS depressants (alcohol, opioids, benzodiazepines, GHB) due to additive sedation, aspiration risk, and loss of airway protective reflexes; avoid stimulants due to additive tachycardia/hypertension and arrhythmia risk; avoid nitrite ‘poppers’ due to compounding hypotension/syncope risk. Drug checking services have repeatedly detected highly potent SCRAs in unexpected products; assume unknown blends may contain more than one SCRA or other psychoactives.

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