COMPOUNDS / COGNITIVE / PANTOGAM
COGNITIVE

PANTOGAM

LOW RISK
BEST FOR:Cognition●●●●●●●○○○7/10
PANTOGAM · HOPANTENIC ACID · PANTOGAM ACTIVE · D-L-GOPANTENIC ACID · GOPANTENIC ACID · HOPANTHENIC ACID · HOMOPANTOTHENIC ACID
NootropicSoviet/RussianGABAergicNeuroprotectiveCognitive EnhancerAnticonvulsant

Russian nootropic and neuroprotective GABA derivative used for cognitive, anxiety, and hyperkinetic disorders.

ROUTE / DOSAGE
LOW250mg
STANDARD500-1000mg
HIGH1800mg
Note: Available as tablets and 10% syrup; pediatric dosing 30-35mg/kg/day
CYCLE
4-12 weeks typical course repeat as clinically indicated
BIOAVAILABILITY
moderate oral (~40-60%)
ACTIVE DURATION
8-12h (subjective)
STORAGE
Room temperature dry away from light
HALF-LIFE
~48h (plasma)
DURATION BREAKDOWN
Total8-12h
Onset1-2h
Come up2-4h
Peak4-8h
Offset4-6h
After effectsminimal
Duration varies by route, dose, and individual. Source: community reports.
§ 01 — EFFECTS
7 documented
Improves cognitive function and attention
Reduces anxiety and emotional lability
Mild psychostimulating activation
Anticonvulsant activity
Reduces hyperactivity and impulsivity in children
Improves social functioning and adaptation
No withdrawal or dependence potential
§ 02 — RISKS
Allergic reactions including skin rash and rhinitis
Sleep disturbances if taken late in day
Possible gastrointestinal discomfort
Tolerance adjustments needed in epilepsy patients
Limited international safety data outside Russian clinical practice
§ 03 — INTERACTIONS
Interaction data not yet available for this compound.
§ 04 — SCIENCE

Pantogam has been studied primarily in Russian clinical settings across diverse populations including children with ADHD, adults with hypertension-related cognitive decline, and schizophrenia patients on antipsychotics. A randomized placebo-controlled trial in children aged 6-12 demonstrated significant reduction of hyperkinetic symptoms over 6 weeks versus placebo. Animal studies show it modulates D2 and GABA-B receptor density in the prefrontal cortex of attention-deficit mice. Clinical trials report cognitive and anxiety improvements within the first week of treatment. However, the evidence base is largely confined to Russian-language publications and lacks large-scale international multicenter trials, limiting generalizability. No addiction, hyperstimulation, or withdrawal syndrome has been reported across studies.

§ 06 — SOURCES
[1]
PubMed PMID 28884730
pubmed.ncbi.nlm.nih.gov ↗
[2]
PubMed PMID 27456906
pubmed.ncbi.nlm.nih.gov ↗
[3]
PubMed PMID 34730553
pubmed.ncbi.nlm.nih.gov ↗
[4]
PubMed PMID 26978493
pubmed.ncbi.nlm.nih.gov ↗
[5]
PubMed PMID 26356612
pubmed.ncbi.nlm.nih.gov ↗
[6]
PubMed PMID 27635617
pubmed.ncbi.nlm.nih.gov ↗
[7]
PubMed PMID 15658299
pubmed.ncbi.nlm.nih.gov ↗
[8]
PubMed PMID 21311483
pubmed.ncbi.nlm.nih.gov ↗
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