Fasoracetam molecular structure

Fasoracetam

(NS-105, AEVI-001, NFC-1)

Fasoracetam is an experimental racetam that acts as an mGluR modulator and failed late-stage trials for vascular dementia and ADHD, but continues to be explored in rare genetic disorders and as a research cognitive enhancer.

Also known as:

NS-105AEVI-001NFC-1LAM-105NB-001

Formula

C₁₀H₁₆N₂O₂

Category

Racetam / mGluR Modulator

Half-Life

4–6.5 hours

Bioavailability

79–97% (rodents)

Chemical Profile

IUPAC Name:(5R)-5-Oxo-D-prolinepiperidinamide
Molecular Formula:C₁₀H₁₆N₂O₂
Structure:Pyroglutamic acid derivative, pyrrolidone ring
PubChem CID:198695
Molar Mass:196.25 g/mol
Bioavailability:79–97% (animals)
Half-life:4–6.5 hours (animals)
Origin:Nippon Shinyaku, Japan, 1980s

Mechanism of Action

Fasoracetam is believed to modulate metabotropic glutamate receptors (mGluR groups 1, 2, and 3), increasing acetylcholine release and normalizing disrupted glutamatergic signaling. These properties are unique among studied racetams.

Preclinical & Clinical Evidence

Cognition Improvement in Animal Models

Fasoracetam demonstrated improvement of cognitive function, including memory and learning, in multiple rodent studies.

ADHD Linked to mGluR Mutations: Nature Communications 2018

In adolescents with ADHD and gene network variants that disrupt mGluR neurotransmitter signaling, Fasoracetam demonstrated some efficacy, but only in this rare subgroup.

Systematic Review of New ADHD Compounds

Broader reviews of RCTs, including those using Fasoracetam for ADHD, conclude that efficacy outside rare gene variant subgroups is limited or disappointing.

Safety & Side Effects

No significant safety signals emerged in published clinical studies, but the number/scale of trials is very limited, and rare effects may be undetected. Human use is not authorized outside research.

No formal, large-scale safety data.

Regulatory & Legal Status

US/EU/International

  • Not FDA- or EMA-approved for any indication
  • Schedule 4 (Rx-only) in Australia
  • Research chemical, not authorized for regular human/clinical use

Note: Not for human use or sale as a supplement.

History & Development

Developed by Nippon Shinyaku in the late 1980s, Fasoracetam underwent phase 3 trials for vascular dementia and later, for rare forms of ADHD. Development has since been largely discontinued except for rare genetic indications.

1980s
Synthesis & Animal Research
2010s
ADHD Trials, mGluR Variant Focus
2020s
Research—Not Marketed
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Benefits

  • Unique mGluR modulator racetam
  • Procognitive effect in animal data
  • First-in-class compound for rare gene variant ADHD/DiGeorge research

Considerations

  • No strong efficacy in general ADHD/human cognition
  • Not FDA/EMA approved; Rx-only AU
  • Not for human use
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