Noopept
N-phenylacetyl-L-prolylglycine ethyl ester
A dipeptide nootropic with Russian clinical use, reported to raise both BDNF and NGF at low oral doses.
Last reviewed · 1 references
How it works
Noopept is a proline-containing dipeptide originally developed as a more potent, orally active relative of piracetam. Rodent work shows increased hippocampal BDNF and NGF expression after repeated dosing, alongside antioxidant and anti-inflammatory effects. Its active metabolite, cycloprolylglycine, is an endogenous neuropeptide.
Early human data. Some human data exists, usually small, open-label, or from a single research group.
What the research reports
- Increased BDNF and NGF mRNA in rat hippocampus with repeated dosing
- Improvement on cognitive measures in Russian trials of mild cognitive impairment
- Anxiolytic effects reported alongside cognitive effects
What it has not been shown to do
- No Western regulatory trials
- No demonstrated benefit in healthy young adults
Dosing reference
Russian clinical use is typically 10–30 mg/day orally, divided across doses.
Calculate my dose for Noopept- Routes studied
- Oral, Intranasal
- Half-life
- Roughly 30–60 minutes for the parent compound; the active metabolite persists longer
- Cycle length in the literature
- Courses of 4–8 weeks are described in the clinical literature
Working out a draw volume from a vial? Use the free reconstitution calculator.
Side effects and contraindications
Reported side effects
- Headache
- Irritability
- Sleep disruption if dosed late
Do not use if
- Pregnancy and breastfeeding
- Severe hepatic or renal impairment
The practice that shares the mechanism
The BDNF/NGF effect in animals only appears with repeated dosing, not a single dose — which mirrors how practice-driven change works. Both reward consistency over intensity.
What amplifies it
- Choline sufficiency (eggs, liver) is commonly reported as reducing the headache
- Sleep, again — every plasticity compound depends on it
Mechanism hubs
Stacks that include it
Common questions
- Technically it is a dipeptide — two amino acids — which makes it the smallest thing on this site that still qualifies. It is orally active, unlike most of the larger peptides here.
Sources & evidence notes
Some human data exists, usually small, open-label, or from a single research group.
Confidence score 7/100
Preliminary
Mechanism only. Nothing here establishes that a person would feel anything.
- 1.
Bulletin of Experimental Biology and Medicine, 2008 · Source (opens in a new tab)
Animal studyLimited gradeRodent or other animal model. Frequently fails to replicate in people.