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    IC-26 molecular structure

    IC-26 Stats & Data

    Win 1161-3
    NPS DataHub
    MW345.51
    FormulaC20H27NO2S
    IUPAC4-ethylsulfonyl-N,N-dimethyl-4,4-di(phenyl)butan-2-amine
    SMILESCCS(=O)(=O)C(CC(C)N(C)C)(c1ccccc1)c1ccccc1
    InChIKeyNLPGJSPLDNDKKZ-UHFFFAOYSA-N
    Chemical Class Opioid
    Psychoactive Class Depressant
    Half-Life Unknown in humans; community estimates 16–28 h based on redose intervals and withdrawal latency (anecdotal).

    Effect Profile

    Curated
    Opioid 5.4

    Moderate euphoria and itching/nausea with mild sedation and pain relief

    Euphoria / Warmth×3
    7
    Analgesia×2
    4
    Sedation / Relaxation×1
    5
    Itching / Nausea×1
    6

    Tolerance & Pharmacokinetics

    drugs.wiki
    Half-Life
    Unknown in humans; community estimates 16–28 h based on redose intervals and withdrawal latency (anecdotal).
    Addiction Potential
    High for physiological dependence. Subjective euphoria often modest, but long duration and accumulation mirror methadone; daily use for a week or more has led to classic opioid withdrawal on cessation per user diaries.

    Tolerance Decay

    Full tolerance 7d Half tolerance 10d Baseline ~21d

    Estimates reflect typical opioid tolerance patterns and user reports: daily use for ~7 days reaches high tolerance; partial reversal over 10–14 days; near-baseline by 3–4 weeks. Data quality is low and based on analogy to methadone plus community reports.

    Cross-Tolerances

    Methadone
    100% ●○○
    Other full μ-agonists (e.g., morphine, oxycodone)
    70% ●○○
    Kratom/7-OH-mitragynine
    50% ●○○

    Harm Reduction

    drugs.wiki

    Justification for harm-reduction additions: (1) Potency variability and causticity: Multiple recent user threads describe severe nasal burn, variable potency vs methadone (≈50–80%), and advise against intranasal or IV use; therefore dose ranges are conservative and insufflation is discouraged. (2) Accumulation risk: Users report long-acting effects and next-day sedation; spacing redoses ≥12–24 h reduces stacking risk. (3) QTc risk inference: Methadone inhibits hERG and prolongs QT; as a close structural analog lacking definitive human data, methiodone should be treated as potentially QT-prolonging—avoid/additively QT-prolonging drugs and consider ECG if using chronically or at higher doses. (4) CYP2B6 interactions: Methadone clearance is driven by CYP2B6; efavirenz/nevirapine markedly reduce methadone levels and precipitate withdrawal—similar interactions are plausible for methiodone, so monitor for underdosing with inducers and for oversedation with inhibitors. (5) Naloxone reversal: For long-acting opioids, repeated doses or infusion may be required due to naloxone’s shorter half-life; monitor for renarcotization. (6) Depressant combinations: TripSit and DrugWise emphasize high overdose risk when opioids are combined with alcohol, benzos, barbiturates, GHB, and gabapentinoids; avoid or use only under medical supervision with rescue naloxone available. (7) Drug checking: Unregulated opioids can be adulterated with fentanyls or nitazenes; lab drug-checking and use of appropriate test strips where available reduce risk—note fentanyl strips do not detect nitazenes. (8) ROA safety: Given frequent reports of harsh acidity, prefer oral capsules or well-diluted solutions; avoid IV/smoking to reduce tissue damage and unpredictable kinetics. (9) Tolerance/withdrawal: Expect rapid tolerance with daily use and prolonged withdrawal resembling methadone; plan spacing and avoid abrupt cessation. (10) Driving/impairment: Long-acting sedation and miosis can persist into the next day; avoid driving and hazardous tasks. First-aid in overdose: support airway/breathing; administer naloxone (repeat as needed) and seek emergency care; monitor for recurrence due to long duration.

    References

    Drugs.wiki References

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