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4-AcO-MET (4-acetoxy-N-methyl-N-ethyltryptamine) is a synthetic tryptamine, the acetate ester of 4-HO-MET and an asymmetric N-alkyl variant of psilacetin. It is generally considered a prodrug that is hydrolyzed to the active 4-HO-MET, an agonist at the 5-HT2A serotonin receptor producing psilocybin-like effects; structure-activity data indicate that O-acetylation attenuates in vitro 5-HT2A potency while preserving agonist efficacy. Its 4-hydroxy metabolite fully substitutes for the hallucinogen DOM in rodent drug-discrimination testing, and in vitro toxicology has identified hERG channel inhibition and QT prolongation as potential cardiac concerns. The compound and its metabolite have been documented in forensic casework and characterized by crystallographic and analytical methods. Controlled human pharmacology is not well established.
- Psilocin-like headspace
- Often reported as gentle and euphoric
- Visual and emotional changes
- Prodrug of 4-HO-MET, a 5-HT2A agonist
- Nausea and stomach upset
- Anxiety or confusion
- Pupil dilation
Mechanism
4-AcO-MET carries an acetyl group at the 4-position that is cleaved in the body to the active 4-HO-MET, paralleling psilocybin's conversion to psilocin. The active form agonizes the receptor, the core of the classic psychedelic state, with supporting activity at other serotonin receptors such as . The overall effect is a serotonergic shift in perception, mood, and thought.
receptor fingerprint
receptoragonist (via active metabolite)
receptoragonist
5-HT2C receptoragonist
Safetyrisks and cautions, not medical advice
As a substituted tryptamine, 4-AcO-MET is expected to be relatively low in physiological toxicity but psychologically intense and poorly studied, so its margins are uncertain. It can cause nausea, anxiety, and disorientation, and should be avoided by anyone with a personal or family history of psychosis or bipolar disorder; combining it with MAOIs or other strongly serotonergic drugs risks serotonin toxicity. Not medical advice.
Subjective profileweighing the evidence above
Not a supplement and not for casual use; this is an unapproved research tryptamine whose safety margins are genuinely unknown. What is known makes it a reasonable psilocybin stand-in for the experienced, but the psychosis, bipolar and serotonergic contraindications are firm.
Resources
This entry is here for reference.
Research
- 2015first citedNovel psychoactive substances (designer drugs): overview and pharmacology of modulators of mono…
- 2021most active year3 papers
- 2023most recentA Fatal Case Report Resulting from the Abuse of the Designer Benzodiazepines Clonazolam and Flu…
- 1.Novel psychoactive substances (designer drugs): overview and pharmacology of modulators of monoamine signaling
- 2.Psilacetin derivatives: fumarate salts of the methyl-ethyl, methyl-allyl and diallyl variants of the psilocin prodrug
- 3.Investigation of the Structure-Activity Relationships of Psilocybin Analogues.
- 4.Cardiotoxic effects of [3-[2-(diethylamino)ethyl]-1H-indol-4-yl] acetate and 3-[2-[ethyl(methyl)amino]ethyl]-1H-indol-4-ol.
- 5.Discriminative Stimulus Effects of Substituted Tryptamines in Rats.
- 6.A Fatal Case Report Resulting from the Abuse of the Designer Benzodiazepines Clonazolam and Flualprazolam in Conjunction with Dried Opium Poppy Pods.
6 listed here; entry last updated August 2026
Reviews
My notesprivate to this device
FAQ
How does 4-AcO-MET compare to psilocybin?
It is broadly psilocin-like and often described as relatively gentle and euphoric, though experiences vary and data are limited.
Is it a prodrug?
Largely yes; it is thought to be deacetylated in the body to the active 4-HO-MET.
What is its core mechanism?
Its active form agonizes the 5-HT2A serotonin receptor, the shared core of classic psychedelics.
Limitations of the evidence
- Limited safety data
Adverse effects
- Nausea and stomach upset
- Anxiety or confusion
- Pupil dilation