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EmergingResearch compoundReference only

Doliracetam

Obscure experimental indolinone racetam from a 1982 Hoechst patent; virtually no human data.

NootropicRacetamRacetamMemoryAcetylcholineGlutamate

Pharmacology

ClassRacetam · Memory
Primary targetCholinergic transmission (proposed, weak modulation)
Targets3 receptor targets
Half-lifeN/A
OnsetN/A
EvidenceReference only
Affected systemsAcetylcholineGlutamate

Contents

WHAT IS DOLIRACETAM?

Detailed overview

Doliracetam (PubChem CID 208851, C16H14N2O2) is an obscure, experimental compound grouped with the racetams and first described in a 1982 Hoechst patent (EP 62887) covering indolinone-2 derivatives with claimed neuroanabolic properties. Chemically it is not a classic pyrrolidinone racetam but an indolin-2-one (oxindole) derivative, 2-(2-oxo-3-phenyl-2,3-dihydro-1H-indol-1-yl)acetamide. A well-defined mechanism of action has never been established in the published literature, and a PubMed search returns no dedicated clinical or preclinical studies. It is one of the most poorly documented racetams, so this entry is provided for reference only.

Mechanism

Uncharacterized (patent-claimed neuroanabolic)

Half-life

N/A

Onset

N/A

Legal status

Unapproved, unmarketed; reference material only

Receptor profile

  • Cholinergic transmissionWeak
  • AMPA glutamate receptorsWeak
  • Neuronal plasticityWeak

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
  • Theoretical choline-depletion headache, as with other racetams; a choline source may help in principle, but this is unproven
  • Unknown long-term safety: never marketed and with no clinical development on record

Contraindications · 3

  • Pregnancy and breastfeeding: no safety data, should be avoided
  • Not a medicine: human clinical trials have not established its safety, any use is experimental
  • Unknown drug interactions: the mechanism is uncharacterized, so co-administration risk cannot be estimated

Related Nootropics

Same therapeutic category

FAQ

FAQ

Obscure experimental indolinone racetam from a 1982 Hoechst patent; virtually no human data.

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Structure & chemistry

TypeNootropic
FormulaC16H14N2O2
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.