Dihexa Dosage, half-life & reference guide

Also known as PNB-0408 · N-hexanoic-Tyr-Ile-(6) aminohexanoic amide

An experimental nootropic that increased new synaptic connections between neurons in rat studies from one lab. Its proposed mechanism, the HGF/MET growth-factor system, rests on a paper retracted in 2025 for fabricated data, and it has never been tested in humans.

Studied range
10–30 mg
How often
Daily
Half-life
Very long
Evidence
●●● Emerging
Routes
Oral, Topical

Studied in research — not a recommendation.

Dihexa dose guide

How it works.

Nootropic peptide derived from angiotensin IV. In rat neurons it increased new synaptic connections; its developers linked it to the HGF/MET growth-factor system, but that paper was retracted in 2025 for fabricated data. The often-quoted "millions of times more potent than BDNF" figure traces to a 2012 press release, not a peer-reviewed paper.

Commonly reported: Sharper word-finding and verbal fluency within the first days, overstimulation or poor sleep at higher doses, and for many, little or no effect. It stays in the body for weeks (long half-life in rats). Very experimental — approach with caution.

Where Dihexa works.

A body with Brain, nerves & sleep lit
  • Brain, nerves & sleep

    In animals. An experimental nootropic that increased new synaptic connections between neurons in rat studies from one lab.

An area lights for what a peptide is used for and what people report, with the evidence beside it. It isn’t a promise that it works there.

Week by week.

What to expect in the first 8 weeks

  1. Day 1–7Community

    Signal comes in fast

    Commonly reported: Dihexa hits differently than most nootropics, with mental sharpness and verbal fluency coming online within the first few days, though many notice little. Users start low and treat disrupted sleep or overstimulation as the signal to back off.

    The science

    Dihexa is a modified angiotensin IV analog that its developers linked to the HGF/c-Met system (the key paper was retracted in 2025 for fabricated data). McCoy et al. 2013 found it increased spines and synapses in rat hippocampal neurons and reversed memory deficits in scopolamine-treated and aged rats; that paper carries a 2021 expression of concern. HGF/Met signaling is also implicated in some cancer biology, so the cancer concern is taken seriously even though it's untested.

    Sources
    • McCoy et al. (2013)

    Updated Sep 2026

  2. Day 7–28Community

    Memory and verbal clarity climb

    Commonly reported by those who respond: sharper memory, faster recall and smoother verbal flow. Users keep the dose conservative — more isn't better with this compound, and overstimulation is the usual first sign of too much.

    The science

    McCoy et al. 2013 showed oral dihexa reversed spatial memory deficits in aged (24-month) rats. It has a long half-life in rats (~12.7 days), so it stays in the body for weeks after the last dose; whether its effects outlast dosing was never measured. Human pharmacokinetics are not characterized.

    Sources
    • McCoy et al. (2013)

    Updated Sep 2026

  3. Day 28–56Community

    Wrap the cycle here

    Community protocols cap the cycle at 4–8 weeks. Dihexa stays in the body for weeks after the last dose, so extending the cycle adds exposure and risk rather than benefit. A long break and a reassessment are the usual next step.

    The science

    Its long half-life in rats (~12.7 days) is one reason the cycle-off convention is long (months, not weeks); no study measured whether synaptic changes outlast dosing. No human chronic dosing data exists; the oncogenic concern via c-Met is theoretical but mechanistically valid.

    Sources
    • McCoy et al. (2013)

    Updated Sep 2026

  4. Any dayAnimal

    What Dihexa is built on

    Dihexa has striking rat cognitive data from one lab and no human clinical trials. The proposed mechanism is unusual: the developers linked it to HGF/Met, but that paper was retracted in 2025, and the same pathway is implicated in cancer biology. Early-stage research compound, approach accordingly.

    The science

    Developed by Joe Harding's lab at Washington State University as an Alzheimer's drug candidate. It was never tested in humans; the licensee abandoned it by 2015, and the company's successor HGF-modulating drug failed a phase 2/3 Alzheimer's trial. In 2025 three of the lab's papers were retracted for falsified or fabricated data, including the HGF/c-Met mechanism paper; McCoy 2013 stands with an expression of concern. c-Met activation is a theoretical oncogenic risk — relevant because the receptor is upregulated in several cancers and dihexa is reported to activate it.

    Sources
    • McCoy et al. (2013)
    • JPET retraction notice (2025)

    Updated Sep 2026

Day 1 is the day you start it.

A typical run.

Run notes

Cycle
4–8 week cycles maximum. It has a long half-life in rats (~12.7 days), so it stays in the body for weeks after the last dose.Community practice — opinions vary. Not a clinical recommendation.
Timing
Once daily oral or topical. Morning preferred — can cause alertness interfering with sleep.
Routes
Oral, Topical (DMSO carrier)
Stacks
Semax, Selank

Safety.

Common side effects

  • Overstimulation
  • Insomnia
  • Anxiety
  • Vivid dreams
  • Potential oncogenic risk (research stage)

Goes with.

  • In the Limitless stack

    Cognitive enhancement & neuroprotection stack

    With Semax and Selank

Questions people ask.

What is Dihexa?

An experimental nootropic that increased new synaptic connections between neurons in rat studies from one lab. Its proposed mechanism, the HGF/MET growth-factor system, rests on a paper retracted in 2025 for fabricated data, and it has never been tested in humans.

How is Dihexa dosed in research?

The research range for Dihexa is 10–30 mg, daily (cycle 4–8 weeks). Studied in research — not a recommendation.

How long does Dihexa last?

The half-life of Dihexa is very long (weeks) — accumulates.

What do people report on Dihexa?

Commonly reported on Dihexa: sharper word-finding and verbal fluency within the first days, overstimulation or poor sleep at higher doses, and for many, little or no effect. It stays in the body for weeks (long half-life in rats). Very experimental — approach with caution.

Is Dihexa safe?

The research basis for Dihexa is emerging: primarily preclinical / limited human data. Common side effects in the library: overstimulation, insomnia, anxiety, vivid dreams and potential oncogenic risk (research stage).

What does Dihexa stack with?

Common stacks for Dihexa: Semax and Selank. Curated stacks with Dihexa: Limitless.

Research.

The literature

Search the latest research

Reference.

Cadence

Daily

Daily (cycle 4–8 weeks)

Half-life

Very long

Very long (weeks) — accumulates

Research basis

●●● Emerging

Primarily preclinical / limited human data

PepVault for iPhone

Track Dihexa in PepVault

Log every dose, with reminders on your schedule. 7 days free on the yearly plan for new subscribers.

Download on the App Store

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