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    aMT Stats & Data

    3-it It-290 It-403 Monase Indopan Alpha-methyltryptamine alphamethyltryptamine αMT
    NPS DataHub
    MW174.25
    FormulaC11H14N2
    CAS299-26-3
    IUPAC1-(1H-indol-3-yl)propan-2-amine
    SMILESCC(N)Cc1cnc2ccccc12
    InChIKeyQSQQQURBVYWZKJ-UHFFFAOYSA-N
    Tryptamines; 2020/5.1 Indol-3-alkylamine; 2021/5.1 Indol-3-alkylamine; 2022/5.1 Indol-3-alkylamine
    Chemical Class Tryptamine
    Psychoactive Class Psychedelic / Stimulant
    Half-Life Unknown in humans; DrugBank lists half-life as not available. Expect long pharmacodynamic effects regardless of elimination kinetics.

    Pharmacology

    DrugBank
    State Solid

    Description

    Indopan (alpha-methyltryptamine) is a stimulant and psychoactive drug which produces effects similar to 3,4-methylenedioxy-N-methylamphetamine (MDMA), despite being structurally dissimilar. It was developed in the 1960's by Upjohn with the intention for use as an antidepressant. In the 1990's, indopan became regulated as a Schedule I controlled substance in the United states.

    Pharmacodynamics

    With 20-30 milligrams, euphoria, empathy and psychedelic effects are noticeable. Side effects reported have included anxiety, restlessness, tachycardia, muscle tension, jaw tightness, headache, nausea, vomiting, and pupil dilation.

    Toxicity

    Long lasting serotonin neuro-toxicity at high doses is potentially possible, and is seen with a close analogue of alpha-methyltryptmaine: alpha-ethyltryptamine.

    Receptor Profile

    Receptor Actions

    Agonists
    5-HT2A receptor agonist (partial)
    Inhibitors
    Serotonin-dopamine-norepinephrine reuptake inhibitor (SNDRI)
    Monoamine oxidase inhibitor (non-selective, reversible, weak at common doses)
    Other
    Serotonin-dopamine-norepinephrine releasing agent (SNDRA)

    Receptor Binding

    serotonin agonist

    History & Culture

    1929–1960s

    Alpha-methyltryptamine appears to have first been described in the scientific literature around 1929, though it remained relatively unstudied until the late 1950s. More intensive research on AMT began in the late 1950s and early 1960s, conducted alongside its close structural relative alpha-ethyltryptamine (aET). The compound was investigated by multiple pharmaceutical companies during this period, with Upjohn in the United States assigning it the code name U-14,164E, while Sandoz researched it under the designation IT-290. During the 1960s, AMT was briefly marketed in the Soviet Union as an antidepressant under the trade name Indopan (sometimes spelled Indopane). The medication was prescribed in tablet form at doses of 5 to 10 milligrams. However, its clinical use was short-lived, and the drug was withdrawn from the market after only a brief period of therapeutic application. The related compound aET saw somewhat broader pharmaceutical use, being sold commercially in the United States as an antidepressant under the brand name Monase before being placed in Schedule I in 1971.

    1960s–2003

    AMT began to see recreational use during the 1960s, concurrent with its pharmaceutical development. The compound was also employed in certain psychotherapeutic studies during this decade. Despite this early use, AMT remained a relatively obscure substance for several decades following its withdrawal from clinical application. The compound experienced renewed interest in the late 1990s when it became one of the first psychoactive tryptamines to be widely sold as a "research chemical" through online vendors. This period marked the beginning of the modern research chemical market, with AMT becoming available to a significantly broader user base through internet commerce. The increased availability and use of AMT during this era eventually led to regulatory action, with the substance being emergency scheduled in the United States in April 2003 and permanently placed in Schedule I in September 2004.

    Subjective Effect Notes

    physical: The physical effects of AMT can be broken down into six components all of which progressively intensify proportional to dosage.

    cognitive: In comparison to more traditional psychedelics such as LSD, DMT and Psilocin, the AMT head space is described as not nearly as deep, insightful or profound.

    Effect Profile

    Curated + 391 Reports
    Psychedelic 8.5

    Strong visuals, headspace, body load, and auditory effects

    Visual Intensity×3
    10102.9
    Headspace Depth×3
    106.21.6
    Auditory Effects×1
    8100.8
    Body Load / Somatic Effects×1
    10105.8
    Catalog Erowid BlueLight
    Empathogen 9.7

    Strong empathy, stimulation, sensory enhancement, and euphoria

    Empathy / Social Openness×3
    105.91.8
    Euphoria / Mood Elevation×2
    97.25.9
    Stimulation×1
    107.57.7
    Sensory Enhancement×1
    10102.4
    Catalog Erowid BlueLight
    Stimulant 6.1

    Strong anxiety/jitters and stimulation with moderate euphoria, mild focus

    Stimulation / Energy×3
    98.2
    Euphoria / Mood Lift×2
    66.0
    Focus / Productivity×2
    54.1
    Anxiety / Jitters×1
    1010
    Catalog Erowid

    Duration Timeline

    Bluelight
    Onset Comeup Peak Offset After Effects
    Oral
    30 minutes - 2.0 hours
    1-2 hours
    2-6 hours
    4-8 hours
    24 hours
    Total: 13-15 hours
    Insufflated
    4-15 minutes
    15-30 minutes
    2-6 hours
    4-8 hours
    24 hours
    Total: 10-16 hours
    Smoked (Freebase)
    4 minutes
    10-19 minutes
    1-3 hours
    2-4 hours
    12 hours
    Total: 10-16 hours

    Empirical Duration

    Erowid Reports
    Onset Come Up Peak Offset
    Oral (46 reports)

    Community Effects

    TripSit
    Positive
    euphoria visual enhancement sociability
    Negative
    nausea vomiting anxiety body load

    Tolerance & Pharmacokinetics

    drugs.wiki
    Half-Life
    Unknown in humans; DrugBank lists half-life as not available. Expect long pharmacodynamic effects regardless of elimination kinetics.
    Addiction Potential
    Low. Not considered physically dependence-forming; psychological compulsion appears uncommon when spaced use is maintained.

    Tolerance Decay

    Full tolerance 1d Half tolerance 7d Baseline ~14d

    Acutely diminished effects if re-dosed within days; spacing of at least 1–2 weeks is commonly recommended in HR communities to minimize tolerance and after-effects.

    Cross-Tolerances

    LSD
    50% ●○○
    Psilocybin/psilocin
    50% ●○○

    Experience Report Analysis

    Erowid BlueLight
    280 Reports
    1997–2025 Date Range
    43 With Age Data
    32 Effects Detected

    Demographics

    Gender Distribution

    Age Distribution

    Reports Over Time

    Effect Analysis

    Erowid + Bluelight

    Effects aggregated from 330 experience reports (280 Erowid + 111 Bluelight)

    330 Reports
    151 Effects Detected
    69 Positive
    50 Adverse
    32 Neutral

    Effect Sentiment Distribution

    Confidence Distribution

    Positive Effects 69

    Stimulation 46.0% 84%
    Euphoria 43.3% 88%
    Color Enhancement 41.2% 84%
    Music Enhancement 40.0% 86%
    Thought Acceleration 34.0% 80%
    Empathy 26.9% 86%
    Patterning 26.0% 86%
    Surface Breathing 26.0% 86%
    Tactile Enhancement 25.0% 70%
    Visual Trails 24.0% 84%
    Joy 24.0% 85%
    Melting/flowing 20.0% 85%
    Body High 19.7% 83%
    Morphing 18.0% 86%
    Sociability Enhancement 18.0% 85%
    Awe 18.0% 82%
    Focus Enhancement 17.9% 70%
    Introspection 17.5% 79%
    Contentment 16.0% 80%
    Geometric Imagery 16.0% 87%

    Adverse Effects 50

    Nausea 51.8% 84%
    Anxiety 38.5% 80%
    Confusion 30.6% 87%
    Body Load 26.0% 78%
    Vomiting 24.0% 90%
    Thought Disorganization 24.0% 80%
    Pupil Dilation 22.7% 89%
    Jaw Clenching 19.7% 86%
    Headache 17.2% 89%
    Muscle Tension 14.5% 80%
    Paranoia 14.0% 80%
    Insomnia 12.0% 82%
    Memory Suppression 10.9% 75%
    Increased Heart Rate 10.0% 70%
    Sweating 9.7% 78%
    Restlessness 8.0% 79%
    Motor Impairment 7.9% 80%
    Focus Suppression 6.0% 77%
    Tremor 6.0% 82%
    Panic 6.0% 85%

    Dose-Response Correlation

    How effect frequency changes across dose levels

    View data table
    Effect Light (n=21) Common (n=54) Strong (n=64) Heavy (n=43)
    Visual Distortions 81.0% 83.3% 73.4% 79.1%
    Nausea 42.9% 59.3% 60.9% 62.8%
    Music Enhancement 28.6% 42.6% 53.1% 53.5%
    Color Enhancement 47.6% 50.0% 46.9% 51.2%
    Stimulation 38.1% 37.0% 48.4% 51.2%
    Anxiety 33.3% 40.7% 46.9% 39.5%
    Euphoria 28.6% 46.3% 42.2% 41.9%
    Sedation 23.8% 35.2% 42.2% 32.6%
    Empathy 14.3% 40.7% 32.8% 37.2%
    Confusion 33.3% 31.5% 37.5% 39.5%
    Auditory Effects 9.5% 18.5% 26.6% 39.5%
    Pupil Dilation 28.6% 16.7% 35.9% 18.6%
    Closed-Eye Visuals 23.8% 20.4% 23.4% 34.9%
    Tactile Enhancement 14.3% 31.5% 32.8% 20.9%
    Focus Enhancement 19.0% 25.9% 15.6% 30.2%

    Subjective Effect Ontology

    Experience Reports

    Structured effect tags extracted from 391 Erowid & Bluelight experience reports using a controlled vocabulary of 220+ canonical effects across 15 domains.

    Auditory

    music enhancement 132 35.9%

    Cognitive

    confusion 101 26.8%

    Emotional

    euphoria 143 46.2% anxiety 127 36.5%

    Gastrointestinal

    nausea 171 51.5%

    Motor

    stimulation 152 47.3%

    Visual

    visual distortions 203 52.8% color enhancement 136 39.5%

    8 unique effects extracted · Derived from Erowid & Bluelight reports

    Dose–Effect Mapping

    Experience Reports

    How reported effects shift across dose tiers, based on 280 experience reports.

    Oral dose range: 30.0–55.0 mg (median 40.0 mg)
    Effect Light (n=21) Common (n=54) Strong (n=64) Heavy (n=43)
    visual distortions
    81%
    83%
    73%
    79%
    nausea
    43%
    59%
    61%
    63%
    music enhancement
    29%
    43%
    53%
    54%
    color enhancement
    48%
    50%
    47%
    51%
    stimulation
    38%
    37%
    48%
    51%
    anxiety
    33%
    41%
    47%
    40%
    euphoria
    29%
    46%
    42%
    42%
    sedation
    24%
    35%
    42%
    33%
    empathy
    14%
    41%
    33%
    37%
    confusion
    33%
    32%
    38%
    40%
    auditory effects
    10%
    18%
    27%
    40%
    pupil dilation
    29%
    17%
    36%
    19%
    closed-eye visuals
    24%
    20%
    23%
    35%
    tactile enhancement
    14%
    32%
    33%
    21%
    focus enhancement
    19%
    26%
    16%
    30%
    body high
    10%
    24%
    16%
    30%
    jaw clenching
    19%
    22%
    17%
    28%
    hospital
    14%
    7%
    12%
    28%
    headache
    10%
    20%
    23%
    26%
    introspection
    24%
    17%
    23%
    23%

    Showing top 20 of 33 effects

    Risk Escalation

    Sentiment Analysis

    Average frequency of positive vs adverse effects across dose tiers

    Light n=21
    10 positive 24.3% 11 adverse 20.8%
    Common n=54
    10 positive 31.9% 11 adverse 21.7%
    Strong n=64
    10 positive 31.6% 13 adverse 23.1%
    Heavy n=43
    10 positive 34.9% 12 adverse 23.1%
    View effect breakdown

    Adverse Effects

    Effect Light (n=21) Common (n=54) Strong (n=64) Heavy (n=43) Change
    Nausea
    43%
    59%
    61%
    63%
    +46%
    Anxiety
    33%
    41%
    47%
    40%
    +18%
    Confusion
    33%
    32%
    38%
    40%
    +18%
    Pupil Dilation
    29%
    17%
    36%
    19%
    -34%
    Jaw Clenching
    19%
    22%
    17%
    28%
    +46%
    Headache
    10%
    20%
    23%
    26%
    +169%
    Muscle Tension
    24%
    15%
    16%
    19%
    -21%
    Sweating
    10%
    7%
    22%
    5%
    -50%
    Memory Suppression
    10%
    7%
    14%
    12%
    +22%
    Motor Impairment
    6%
    11%
    14%
    +150%
    Increased Heart Rate
    10%
    13%
    8%
    9%
    -2%
    Psychosis
    10%
    5%
    -50%
    Thought Loops
    5%
    0%
    Seizure
    3%
    0%

    Positive Effects

    Effect Light (n=21) Common (n=54) Strong (n=64) Heavy (n=43) Change
    Music Enhancement
    29%
    43%
    53%
    54%
    +87%
    Color Enhancement
    48%
    50%
    47%
    51%
    7%
    Stimulation
    38%
    37%
    48%
    51%
    +34%
    Euphoria
    29%
    46%
    42%
    42%
    +46%
    Empathy
    14%
    41%
    33%
    37%
    +160%
    Tactile Enhancement
    14%
    32%
    33%
    21%
    +46%
    Focus Enhancement
    19%
    26%
    16%
    30%
    +58%
    Body High
    10%
    24%
    16%
    30%
    +217%
    Introspection
    24%
    17%
    23%
    23%
    -2%
    Creativity Enhancement
    19%
    4%
    5%
    9%
    -51%

    Dosage Distribution

    Dose distribution from experience reports

    Median: 40.0 mg IQR: 30.0–55.0 mg n=174

    Real-World Dose Distribution

    62K Doses

    From 348 individual dose entries

    Insufflated (n=15)

    Median: 16.0mg 25th: 7.5mg 75th: 32.5mg 90th: 56.0mg
    mg/kg median: 0.203 mg/kg 75th: 0.449

    Oral (n=287)

    Median: 40.0mg 25th: 29.0mg 75th: 50.0mg 90th: 74.0mg
    mg/kg median: 0.532 mg/kg 75th: 0.76

    Smoked (n=15)

    Median: 12.5mg 25th: 6.5mg 75th: 25.0mg 90th: 30.0mg
    mg/kg median: 0.178 mg/kg 75th: 0.331

    Common Combinations

    Most co-occurring substances in experience reports

    Form / Preparation

    Most common forms and preparations reported

    Body-Weight Dosing

    Dose relative to body weight from reports with weight data

    Oral

    Median: 0.58 mg/kg IQR: 0.394–0.784 mg/kg n=162

    Insufflated

    Median: 0.267 mg/kg IQR: 0.17–0.649 mg/kg n=7

    Redose Patterns

    Redosing behavior across 212 reports

    19.8% Redosed
    1.3 Avg Doses
    60m Median Interval

    Legal Status

    Not under international control (as of 2014)
    Country Status Notes
    Australia Controlled (analogue) Controlled as an analogue of 5-MeO-AMT, which is a Schedule 9 prohibited substance under the Poisons Standard. Possession, production, and sale are illegal. Reportedly listed on Schedule 8 of the Australian Customs import list since 2001.
    Austria NPSG Group 6 Controlled under the Neue-Psychoaktive-Substanzen-Gesetz (New Psychoactive Substances Act). Possession, production, and sale are prohibited.
    Canada Not specifically scheduled Not mentioned in the Controlled Drugs and Substances Act. May still be subject to analogue provisions if sold for human consumption.
    China Controlled Classified as a controlled substance as of October 2015. Production, sale, import, and export are prohibited.
    Denmark List B Placed on List B of controlled substances by the Danish Minister for the Interior and Health in 2010.
    Finland Controlled Classified as a controlled drug under Finnish national drug legislation.
    Germany Anlage I BtMG Listed in Anlage I (Schedule I) of the Betäubungsmittelgesetz (Narcotics Act) since January 31, 1993. Manufacturing, possession, import, export, purchase, sale, and dispensing without license are prohibited.
    Greece Controlled Prohibited under Law 4139/2013. Became a controlled substance on February 18, 2003. Possession, production, and sale are illegal.
    Hungary Schedule C Placed on the Schedule C list of controlled substances in 2013.
    Japan Controlled Made illegal on April 17, 2005. Possession, production, and sale are prohibited.
    Latvia Schedule I Classified as a Schedule I controlled substance under Latvian drug legislation.
    Lithuania List I Controlled as a tryptamine derivative since 2012, listed on the 1st list of Narcotic Drugs and Psychotropic Substances. Medical use is prohibited.
    Russia Controlled AMT and certain derivatives have been controlled substances since June 4, 2012. Possession, production, and sale are illegal.
    Slovakia Controlled Placed on the List of Hazardous Substances in Annex, § 2 in 2013.
    Slovenia Controlled Listed on the Decree on Classification of Illicit Drugs since 2013.
    Spain Legal Not specifically controlled under Spanish drug legislation as of available sources, though some references cite control under general prohibition laws.
    Sweden Controlled Classified as a health hazard under Lagen om förbud mot vissa hälsofarliga varor (Act on the Prohibition of Certain Goods Dangerous to Health) since March 1, 2005 via regulation SFS 2005:26. Sale and possession are illegal.
    Switzerland Verzeichnis D Specifically named as a controlled substance alongside AET under Verzeichnis D (Schedule D) of Swiss controlled substances legislation.
    United Kingdom Class A Made illegal on January 7, 2015 as a Class A drug under the Misuse of Drugs Act 1971 following an Advisory Council on the Misuse of Drugs recommendation to update the tryptamine catch-all clause. Previously uncontrolled because its alkyl substitution occurs on the alpha carbon rather than the nitrogen position.
    United States Schedule I Temporarily placed in Schedule I on April 4, 2003 under emergency scheduling procedures, then permanently scheduled on September 29, 2004. Classified as a hallucinogen with high abuse potential and no accepted medical use. Also listed as a dangerous drug in Arizona since April 2014 and Schedule I in Illinois.

    Harm Reduction

    drugs.wiki

    AMT is a long-acting serotonergic tryptamine with stimulant and entactogenic features; nausea and vomiting are common, especially early in the experience. Onset is often slow (60–180 minutes), which leads some to redose prematurely; this is a frequent cause of overdosing—wait at least 2.5–3 hours before considering any change. AMT’s serotonergic action and reported mild MAOI activity mean combinations with other serotonergic agents (e.g., SSRIs/SNRIs/TCAs, MAOIs, MDMA, tramadol, dextromethorphan, linezolid, St John’s Wort) significantly increase the risk of serotonin syndrome; avoid these mixes entirely. Distinguish AMT from 5-MeO-AMT: 5-MeO-AMT is active at single-digit milligram doses and has been linked to medical emergencies; confusing the two has led to overdoses—verify substance identity via trusted drug checking. Because AMT is sometimes sold as different salt forms (e.g., succinate) or freebase, be aware that equal milligram weights may not equal the same base amount; if the salt form is unknown, start at the very low end. Insufflation and smoking/freebasing produce faster, sharper onsets and are associated with more nausea, irritation, and anxiety; oral use is generally better tolerated. Plan for the very long duration and potential insomnia: avoid driving/operating machinery until the next day and keep the environment cool, with periodic fluids and electrolytes to mitigate hyperthermia risk if exerting. Use an accurate milligram scale and avoid eyeballing; if volumetric dosing is used, label clearly and measure precisely. Given variable potency and common misrepresentation in the unregulated market, use professional drug checking where available and avoid polydrug use.

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