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Nootropics / Racetams and ampakines

61 In the index

Sunifiram SUNI

A very potent brain-supplement compound in rodent studies, working at surprisingly low doses. It has never been tested in human clinical trials, so its safety in people is essentially unknown despite its popularity in gray-market sales.

Also known as DM-235, Piperazine, 1-benzoyl-4-(1-oxopropyl)-, 66924E735K, 1-(4-benzoyl-1-piperazinyl)-1-Propanone, RefChem:907342, 1-(4-benzoylpiperazin-1-yl)propan-1-one, DM 235, Sunifiram DM235

Effects Focus
Routes Oral
Legal status Research chemical
WADA Not listed

3D Molecular Structure of C14H18N2O2

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  • Carbon
  • Hydrogen
  • Nitrogen
  • Oxygen

Chemistry

Formula
C14H18N2O2
Molar mass
246.30
CAS
314728-85-3
PubChem CID
4223812
IUPAC name
1-(4-benzoylpiperazin-1-yl)propan-1-one
InChIKey
DGOWDUFJCINDGI-UHFFFAOYSA-N

Reported dosing

User-reported

What has been reported in the literature and by users. This is a record of what is done, not a recommendation.

Typical dose 4-8 mg
Reported range 4-10 mg/day
Route Oral or sublingual
Frequency Once or twice daily
Duration Not established

A very potent experimental ampakine-family compound with no completed human clinical trials; nearly all data comes from rodent studies, and dosing circulating online is anecdotal, not evidence-based.

Where this comes from Animal studies only; anecdotal biohacker reports

There is no approved human dosing for this compound. The figures above are what users and vendors report, not what has been established as safe or effective. Treat them as a record of what is done, not as guidance.