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EmergingResearch compoundReference only

Dupracetam

Obscure experimental dimer-type racetam (bis-pyrrolidinone hydrazide); virtually no human data.

NootropicRacetamRacetamAcetylcholineAcetylcholineGlutamate

Pharmacology

ClassRacetam · Acetylcholine
Primary targetProposed modulation of cholinergic transmission
Targets3 receptor targets
Half-lifeN/A
OnsetN/A
EvidenceReference only
Affected systemsAcetylcholineGlutamate

Contents

WHAT IS DUPRACETAM?

Detailed overview

Dupracetam is an obscure, experimental racetam whose structure links two 2-pyrrolidinone (2-oxopyrrolidine) rings through a hydrazide bridge (a bis-pyrrolidinone hydrazide dimer). In preclinical animal work it antagonized the lethality of hemicholinium-3 in mice (30-300 mg/kg), suggesting facilitation of cholinergic transmission such as acetylcholine release, but the precise molecular target was never established. Clinical development was not completed: there are no Phase III trials, and the evidence derives almost entirely from animal models. One metabolite, 1-methylhydantoin, showed renal toxicity at high doses, so this entry is provided for reference only.

Mechanism

Proposed cholinergic (unconfirmed)

Half-life

N/A

Onset

N/A

Legal status

Unapproved, experimental compound

Receptor profile

  • Cholinergic transmissionWeak
  • AMPA glutamate receptorsWeak
  • NeuroprotectionWeak

Safety

Side effects, stop signs, contraindications

Side effects · 3

  • With virtually no human data, the side-effect profile is unknown; racetam-like effects such as headache are plausible but unconfirmed
  • One metabolite, 1-methylhydantoin, showed renal toxicity at high doses in preclinical models; this is a theoretical concern
  • Unknown long-term safety: never marketed and clinical development was not completed

Contraindications · 3

  • Pregnancy and breastfeeding: no safety data, should be avoided
  • Renal impairment: caution or avoidance is warranted given the nephrotoxic metabolite (1-methylhydantoin)
  • Not a medicine, unknown interactions: the mechanism is uncharacterized, so co-administration risk cannot be estimated and any use is experimental

Related Nootropics

Same therapeutic category

Studies

Related research and clinical findings

FAQ

FAQ

Obscure experimental dimer-type racetam (bis-pyrrolidinone hydrazide); virtually no human data.

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Structure & chemistry

TypeNootropic
FormulaC12H18N4O4
UpdatedJuly 9, 2026
MolekulaX Editorial Team·Source-verified · PubMed · FDA · EMA
Updated: July 9, 2026

The information here is strictly for educational and scientific purposes. It does not replace medical advice or clinical consultation, and it does not encourage illegal substance or pharmaceutical use. Data is sourced. When in doubt, consult your doctor.