Fat-soluble compound requiring dietary fat for optimal absorption. Oral bioavailability of parent drug is very low (~10%); most central activity believed to come from active metabolites (notably N-anisoyl-GABA and 2-pyrrolidinone). Users often stack with choline sources (CDP-choline, alpha-GPC) to reduce racetam-type headaches, though clinical necessity is unproven. Produces mild anxiolysis in some users without cognitive dulling. Not approved by U.S.
Анирацетам molecular structure diagram from the DrugsPRO substance library.
Also known as: Sarpul, Sarple, Ampamet, Referan, Draganon, Sarple/Sarpul
Classification
Chemical: Racetam
Psychoactive: Depressant
Psychoactive: Nootropic
Tag: Research-Chemical
Effects
Creativity Enhancement
Stimulation
Sedation
Motor Impairment
Nausea
Headache
Anxiety Suppression
Focus Enhancement
Memory Enhancement
Motivation Enhancement
Thought Connectivity
Analysis Enhancement
Color Enhancement
Visual Acuity Enhancement
Music Enhancement
Open Eye Visuals
Dulled Perception
Appetite Suppression
Routes of Administration
Oral
Dosage
Threshold: 200 mg
Light: 500 – 750 mg
Common: 750 – 1,500 mg
Strong: 750 mg
Heavy: 750 mg
Duration
Onset: 0.8-1.5 h
Comeup: 0.5-1 h
Peak: 1-2 h
Offset: 1-2 h
After Effects: 1-4 h
Total Duration: 2-5 h
Sublingual
Dosage
Threshold: 150 mg
Light: 300 – 500 mg
Common: 500 – 1,000 mg
Strong: 500 mg
Heavy: 500 mg
Duration
Onset: 0.08-0.33 h
Comeup: 0.25-0.5 h
Peak: 0.75-1.5 h
Offset: 1.5-3 h
After Effects: 1-4 h
Total Duration: 2-4 h
Harm Reduction
Check interactions before mixing substances, pay attention to dose spacing and hydration, and treat all dosage guidance as approximate rather than guaranteed safe.
Sources
Substance data is aggregated from the following public harm-reduction and reference sources.
This static page is intended as a readable non-JS and prerender-friendly library export.
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Aniracetam - DrugsPRO vodič o supstancama
Aniracetam: Fat-soluble compound requiring dietary fat for optimal absorption. Oral bioavailability of parent drug is very low (~10%); most central activity believed to come from active metabolites (notably N-anisoyl-GABA and 2-pyrrolidinone). Users often stack with choline sources (CDP-choline, alp
