COMPOUNDS / PSYCHIATRIC / AFOBAZOL
PSYCHIATRIC

AFOBAZOL

LOW RISK
BEST FOR:Anxiety●●●●●●●○○○7/10
AFOBAZOL · FABOMOTIZOLE · AFOBAZOLE · FABOMOTIZOLE DIHYDROCHLORIDE
AnxiolyticNeuroprotectiveSoviet / RussianSigma-1Antioxidant

Russian-developed selective anxiolytic acting on sigma-1 receptors with neuroprotective properties and no sedation or dependence liability.

ROUTE / DOSAGE
LOW5mg
STANDARD10mg
HIGH20mg
Note: Taken 3x daily; therapeutic effect builds over 5-7 days of regular use, peak at ~4 weeks
CYCLE
2-4 week treatment course daily use
BIOAVAILABILITY
~0.5% oral
ACTIVE DURATION
4-6h per dose therapeutic effect sustained with 3x daily dosing (subjective)
STORAGE
Room temperature dry away from light
HALF-LIFE
1.2h (plasma)
DURATION BREAKDOWN
Total4-6h
Onset5-7 days
Come up1-2 weeks
Peak3-4 weeks
Offset1-2 weeks
After effects1-2 weeks
Duration varies by route, dose, and individual. Source: community reports.
§ 01 — EFFECTS
7 documented
Reduced anxiety without sedation
Mild activating/stimulating component
No muscle relaxation or ataxia
No cognitive impairment
Neuroprotective antioxidant effects
Improved stress tolerance
No withdrawal or dependence reported
§ 02 — RISKS
Potential MAO-A inhibition may interact with serotonergic drugs
Delayed onset means acute anxiety episodes are not addressed
Limited international clinical data; evidence primarily from Russian studies
Angiogenic activity reported in vitro, clinical significance unknown
Not approved by FDA or EMA; quality of sourcing may vary
§ 03 — INTERACTIONS
Interaction data not yet available for this compound.
§ 04 — SCIENCE

Afobazol was developed in Russia based on a pharmacogenetic concept of anxioselectivity and has been clinically used there since the early 2000s. In vitro studies demonstrate neuroprotective effects against oxidative stress and glutamate toxicity in HT-22 neurons. Animal studies show efficacy in experimental cerebral hemorrhage models, improving survival, learning, and motor activity. Clinical trials in 30 patients confirmed anxiolytic action with an activating component and absence of sedative or myorelaxant effects. However, all published evidence comes from Russian research groups, and no large-scale international randomized controlled trials exist. The compound is not approved by the FDA or EMA, limiting its evidence base relative to mainstream anxiolytics.

§ 06 — SOURCES
[1]
Neuroprotective properties of afobazol in vitro
pubmed.ncbi.nlm.nih.gov ↗
[2]
Sigma-2 receptor ligands: neurobiological effects
pubmed.ncbi.nlm.nih.gov ↗
[3]
Neuroprotective effects of afobazol in experimental cerebral hemorrhage
pubmed.ncbi.nlm.nih.gov ↗
[4]
Studies of long-term noopept and afobazol treatment in rats with learned helplessness neurosis
pubmed.ncbi.nlm.nih.gov ↗
[5]
Angiogenic Effects of Anxiolytic Fabomotizole
pubmed.ncbi.nlm.nih.gov ↗
[6]
Clinical study of the selective anxiolytic agent afobazol
pubmed.ncbi.nlm.nih.gov ↗
[7]
The antimutagenic activity of afobazol studied in vivo
pubmed.ncbi.nlm.nih.gov ↗
[8]
Neurochemical study of effects of afobazol and ladasten on monoamine synthesis and metabolism
pubmed.ncbi.nlm.nih.gov ↗
Disclaimer. Protokol.wiki is an informational reference. Nothing on this site is medical advice. Compounds listed may be unapproved, unregulated, or illegal in your jurisdiction. Consult a licensed physician before use. Data compiled from peer-reviewed literature.
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