DIHEXA 5 mg
Dragon Pharma

DIHEXA 5 mg

Product Information Compound Details
Dragon Pharma
Active Substance DIHEXA Angiotensin IV analog (PNB-0408)
5 mg/vial
Strength 5 mg/vial
Package 2 mL Vial Lyophilized powder
Form Lyophilized Powder
Drug Class Research Peptide
Manufacturer Dragon Pharma
Half-Life Approximately 12.7 Days
Out of stock
Product Overview

DIHEXA 5 mg by Dragon Pharma

DIHEXA 5 mg is a lyophilized research peptide manufactured by Dragon Pharma, supplied as 5 mg per 2 mL vial for laboratory research purposes.

DIHEXA Injectable

DIHEXA 5 mg contains DIHEXA (N-hexanoic-Tyr-Ile-(6) aminohexanoic amide), also known as PNB-0408, a synthetic oligopeptide derived from angiotensin IV . It is a small molecule with a molecular weight of 504.66 Da and the formula C27H44N4O5 . DIHEXA was designed to address the pharmacokinetic limitations of earlier angiotensin IV analogs: it is orally bioavailable, crosses the blood-brain barrier, and has an extended circulating half-life of approximately 12.7 days after intravenous administration in rats .

The proposed mechanism of action for DIHEXA involves potentiation of hepatocyte growth factor (HGF) signaling through its receptor c-Met. DIHEXA binds to HGF with high affinity and augments its activity at subthreshold concentrations, inducing c-Met phosphorylation . This downstream activation of the HGF/c-Met pathway has been associated with hippocampal spinogenesis and synaptogenesis in preclinical models . In a 2021 study using APP/PS1 Alzheimer's model mice, DIHEXA administration restored spatial learning and cognitive function in the Morris water maze test, increased neuronal cell counts, and reduced neuroinflammatory markers .

DIHEXA is not FDA-approved for any indication, has no investigational new drug status, and is sold strictly as a research chemical . The evidence base for DIHEXA is entirely preclinical, and it carries significant scientific caveats: a key 2013 paper carries an expression of concern regarding possible image manipulation, and a 2014 follow-up paper was retracted in 2025 . More critically, the HGF/c-Met pathway that DIHEXA activates is the same pathway that, when overactive, contributes to tumor growth and cancer progression . No long-term safety data exists in animals or humans .

Key Benefits of DIHEXA 5 mg

  • Angiotensin IV analog studied for cognitive and neurotrophic effects in preclinical models
  • Orally bioavailable and blood-brain barrier permeable
  • Extended half-life of approximately 12.7 days in animal studies
  • Lyophilized powder format for reconstitution and laboratory use
  • 5 mg vial strength supports extended research protocols
Formulation

Lyophilized Powder

DIHEXA 5 mg is supplied as a lyophilized powder in a 2 mL vial. The powder requires reconstitution with an appropriate solvent before laboratory use. DIHEXA is highly fat-soluble and poorly water-soluble, which is relevant to solvent selection .

Product Profile

DIHEXA Profile

DIHEXA is a synthetic angiotensin IV analog that potentiates HGF/c-Met signaling, studied for its effects on synaptic connectivity and cognition in preclinical models.

Angiotensin IV Analog (HGF Mimetic)

DIHEXA belongs to the class of angiotensin IV (AngIV) analogs. AngIV is a naturally occurring hexapeptide (Val-Tyr-Ile-His-Pro-Phe) that has been studied for its effects on learning, memory, and cerebral blood flow . DIHEXA was developed through structural modifications of the AngIV scaffold to improve metabolic stability, blood-brain barrier permeability, and oral bioavailability. Its structure consists of an N-hexanoic acid cap linked to a tyrosine-isoleucine core with a C-terminal 6-aminohexanoic amide modification .

The pharmacokinetic profile of DIHEXA is distinguished by its extended duration. In adult male Sprague-Dawley rats, DIHEXA demonstrated a circulating half-life of 12.68 days after intravenous administration and 8.83 days after intraperitoneal administration . This long half-life means that repeated daily dosing leads to significant accumulation in the bloodstream over time . DIHEXA has approximately 38% oral bioavailability in animal models .

The proposed mechanism involves HGF/c-Met pathway potentiation. HGF is a growth factor that activates the c-Met receptor tyrosine kinase, which plays roles in cell proliferation, survival, and motility. DIHEXA binds HGF and enhances its ability to activate c-Met at concentrations that would otherwise be insufficient . This activation triggers downstream signaling cascades including PI3K/AKT, which promotes neuronal survival and synaptic plasticity . However, the same pathway is implicated in cancer biology, and there is a theoretical concern that activating it could promote tumorigenesis .

Half-Life

Approximately 12.7 Days

DIHEXA has a circulating half-life of 12.68 days after IV administration in rats . This unusually long half-life for a peptide means that daily dosing leads to accumulation. By week 4 of daily use, plasma levels would reflect 4 to 5 half-lives of accumulation .

DIHEXA 5 mg vs Other Dragon Pharma Preparations

Dragon Pharma offers a range of research peptides. DIHEXA 5 mg is positioned as a neurotrophic research compound with a distinct mechanism, complementing other peptide products.

For other cognitive research peptides, Dragon Pharma offers Semax and Selank, which act through different neurotrophic pathways. For mitochondrial research compounds, MOTS-C and SS-31 target cellular energy metabolism rather than synaptic connectivity. For general research peptides, BPC 157 is also available.

Dosage & Usage

DIHEXA 5 mg Dosage & Usage

The information below is provided for educational reference only. DIHEXA is a research compound that has never been approved for human use. No human safety or efficacy data exists, and the evidence base for its cognitive effects is entirely preclinical. Non-medical use falls outside any approved indications and carries serious unknown risks, including theoretical concerns about cancer pathway activation.

Typical Dosage Ranges

No established human dosage exists for DIHEXA. In preclinical research, the most cited dose is 2 mg/kg/day orally in aged rats and scopolamine-impaired rats . In non-medical community contexts, oral doses of 5–20 mg daily are referenced, with some users reporting doses as high as 40 mg daily . The community dosing range is extrapolated from rat studies using allometric scaling, but human-equivalent doses cannot be reliably calculated from rodent data . A 5 mg dose is 5,000 mcg, which is 10 to 100 times higher than typical peptide doses, making unit verification critical .

Use Case Common Reference Range Frequency
Preclinical research (rat) 2 mg/kg/day Once daily, oral
Non-medical (low reference) 5–10 mg Once daily
Non-medical (higher reference) 10–20 mg Once daily
Non-medical (aggressive) 20–40 mg Once daily

Community doses are extrapolated from animal studies and are not validated by human clinical trials. DIHEXA has no established human dosing.

Stacking & Cycle Considerations

DIHEXA is not an anabolic compound and is not stacked for muscle-building purposes. In non-medical research contexts, it is sometimes referenced alongside other cognitive peptides. Community discussions describe combining DIHEXA with Semax for a cognitive stack targeting both synaptogenesis and BDNF upregulation . For neuroprotective research, Cerebrolysin is sometimes referenced in combination, though no clinical data exists on such combinations.

Because DIHEXA has an unusually long half-life, accumulation is a significant consideration. Community protocols reference cycling patterns of 90 days on followed by 30 days off, or shorter cycles of 4–8 weeks with equal time off . The long half-life means that even after stopping, the compound may remain active in the body for weeks .

Managing Side Effects

No human safety data exists for DIHEXA. Anecdotal community reports describe headaches, brain fog, fatigue, irritability, and mood changes . These reports are not a safety profile and cannot substitute for controlled clinical data. There is no published chronic toxicology, genotoxicity, reproductive toxicity, or carcinogenicity data for DIHEXA in humans .

The most significant safety concern is theoretical but serious: DIHEXA activates the HGF/c-Met pathway, which is implicated in cancer progression when dysregulated . The FDA has approved cancer drugs specifically to block c-Met, and a compound that stimulates this pathway with no long-term safety data raises a legitimate concern that has not been studied . Individuals with a personal or family history of cancer should be particularly cautious .

Product quality is another practical risk. Independent testing found that 9 of 12 commercial DIHEXA samples were below 95% purity . A batch-specific HPLC and mass spec COA from an independent third-party lab is often recommended, but this does not address the fundamental safety questions .

Post-Cycle Therapy

DIHEXA is not part of any post-cycle therapy protocol. It has no relationship to the hypothalamic-pituitary-gonadal axis, and its research focus has been on synaptic connectivity and cognition. PCT compounds such as Clomid and Nolvadex address entirely different biological systems.

Important

Research Use Only

DIHEXA has never been approved for human use. Its evidence base is entirely preclinical, a key supporting study was retracted, and its mechanism raises theoretical cancer concerns. The information above is for educational reference and does not constitute medical advice. Human use is not recommended.

Safety & Information

DIHEXA Safety Information

DIHEXA is an experimental research compound that has never been approved for human use. No human safety data exists, and the compound's mechanism of action raises unresolved theoretical concerns about cancer pathway activation.

Important Safety Information

DIHEXA is not FDA-approved for any indication. It has no approved label, no investigational new drug status, and is sold online as a research chemical with the disclaimer "not for human consumption" . This means purity, dosing accuracy, and sterility are not regulated or verified by any authority . Independent testing found significant purity issues in commercial samples .

Important

Not for Human Use

DIHEXA 5 mg is sold strictly for research purposes. It is not a dietary supplement, medication, or approved therapeutic agent. Human consumption for cognitive enhancement or any other purpose is not recommended and may pose serious health risks.

Potential Adverse Effects

No human safety data exists for DIHEXA. There is no published chronic toxicology, genotoxicity, reproductive toxicity, or carcinogenicity data in humans . Anecdotal community reports describe headaches, brain fog, fatigue, irritability, and mood changes, but these are not a safety profile and cannot substitute for controlled clinical data .

The most significant concern is theoretical but serious: DIHEXA activates the HGF/c-Met pathway, which is a known oncogenic signaling axis when overactive . The FDA has approved drugs specifically to inhibit c-Met for cancer treatment. A compound that stimulates this pathway, with no long-term human safety data, raises a legitimate concern that has not been studied .

Additional concerns include the retraction of a key 2014 mechanistic study due to data integrity issues, which weakens the evidence base for the compound's proposed mechanism . The long half-life of DIHEXA means that repeated dosing leads to accumulation, which could amplify any adverse effects .

Conditions Requiring Medical Evaluation

DIHEXA has no approved indications and no established contraindications because no human use is supported. However, given the mechanism of action, individuals with a personal or family history of cancer should be particularly cautious . No human reproductive or developmental toxicology data exists, so pregnant or breastfeeding individuals should avoid it .

Monitoring During Therapy

No monitoring protocols exist for DIHEXA because it has no approved human use. In research settings, standard laboratory safety monitoring would apply. For any hypothetical human use, monitoring of tumor markers and comprehensive metabolic panels is sometimes referenced in community discussions, but this is not evidence-based .

Product Care

Storage & Handling

Store lyophilized powder at -20°C, protected from light and moisture . Reconstituted solutions should be stored at 2-8°C and used promptly . DIHEXA is highly fat-soluble and poorly water-soluble, which affects solvent selection . Keep all research compounds out of the reach of children.

Shipping & Authenticity

Shipping & Product Authenticity

DIHEXA 5 mg is supplied through the official Dragon Pharma distribution chain and shipped in original manufacturer packaging with discreet, privacy-focused handling.

USA Domestic 3–5 business days
International 10–15 business days
Order Processing 24–48 business hours
Tracking Provided after dispatch
Direct Supply

Discreet Delivery & Original Packaging

The outer shipping package remains discreet, with privacy-focused handling and no unnecessary external product details. Products are supplied through the official Dragon Pharma distribution chain.

What to Expect

  • Orders are processed after payment confirmation
  • USA Domestic shipping is typically faster when local stock is selected
  • International orders include tracking, though update frequency may vary by destination
  • Multiple warehouses may result in separate shipments when applicable

Authenticity Verification

To verify your DIHEXA 5 mg product, use the security code on the packaging and cross-check it on the Dragon Pharma official site. Official Dragon Pharma presentation and original packaging help reinforce product legitimacy and buyer confidence.

Storage

DIHEXA 5 mg Storage

Proper storage conditions help preserve peptide integrity and stability throughout shelf life.

Recommended Conditions

Store lyophilized powder at -20°C, protected from light and moisture . Keep the vial in its original packaging until use. Reconstituted solutions should be stored at 2-8°C and used promptly; long-term stability data for reconstituted solutions have not been published .

DIHEXA is highly fat-soluble and poorly water-soluble, which affects solvent selection for reconstitution . Do not use if the solution appears cloudy or discolored. Keep out of reach of children.

Quick Reference

Do & Don't

  • Do store lyophilized powder at -20°C
  • Do keep in original packaging
  • Do refrigerate reconstituted solution at 2-8°C
  • Don't expose to light or moisture
  • Don't store reconstituted solution long-term
  • Don't use if solution is cloudy or discolored
Frequently Asked Questions

DIHEXA 5 mg FAQ

Answers to common questions about DIHEXA 5 mg, its research status, mechanism of action, and safety considerations.

What is DIHEXA 5 mg used for?

DIHEXA 5 mg is a research peptide studied for its effects on synaptic connectivity and cognition in preclinical models. It is an angiotensin IV analog that potentiates HGF/c-Met signaling . It has never been approved for human use and is sold strictly for laboratory research purposes.

How often should DIHEXA 5 mg be used?

No established human dosage exists. In animal studies, 2 mg/kg/day orally was used . In non-medical community contexts, oral doses of 5-20 mg daily are referenced . DIHEXA has a half-life of approximately 12.7 days, which means it accumulates with daily dosing .

Does DIHEXA 5 mg require PCT?

DIHEXA has no relationship to the hypothalamic-pituitary-gonadal axis and is not part of any post-cycle therapy protocol. Its research focus has been on synaptic connectivity and cognition, not hormonal recovery. PCT compounds such as Clomid and Nolvadex address entirely different biological systems.

What does DIHEXA do?

DIHEXA is an angiotensin IV analog that binds to hepatocyte growth factor (HGF) with high affinity and potentiates its activity at the c-Met receptor . This activation of the HGF/c-Met pathway has been associated with hippocampal spinogenesis and synaptogenesis in preclinical models . In a 2021 study, DIHEXA restored cognitive function in APP/PS1 Alzheimer's model mice .

How long does DIHEXA take to work?

No human data exists on the time course of DIHEXA effects. In animal studies, cognitive improvements were observed over treatment periods of weeks to months . DIHEXA has a half-life of approximately 12.7 days, which means steady-state levels accumulate slowly over several weeks of daily dosing .

Is DIHEXA the best cognitive peptide?

There is no single cognitive peptide that is universally best, and DIHEXA's evidence base is particularly weak. A key 2014 study was retracted, and no human trials have been conducted . Other research peptides like Semax have different mechanisms and evidence profiles. The appropriate choice depends on research goals and a careful assessment of available evidence.

What is the difference between DIHEXA and Semax?

DIHEXA and Semax have different mechanisms. DIHEXA is an angiotensin IV analog that potentiates HGF/c-Met signaling, while Semax is a synthetic ACTH fragment that upregulates BDNF and modulates other neurotrophic pathways. Both are research peptides with different evidence bases and proposed applications.

What is the difference between DIHEXA and Cerebrolysin?

DIHEXA and Cerebrolysin are fundamentally different. DIHEXA is a small synthetic angiotensin IV analog that potentiates HGF/c-Met signaling. Cerebrolysin is a mixture of neurotrophic peptides and amino acids derived from pig brain. They have different compositions, mechanisms, and evidence bases.

Is 5 mg of DIHEXA a lot?

No human dosing standards exist for DIHEXA. The 5 mg vial strength is a research quantity. In non-medical community contexts, 5-20 mg daily is referenced, so a 5 mg vial provides 1-4 doses depending on the protocol. DIHEXA is dosed in milligrams, not micrograms, which is unusual for peptides .

What strength is DIHEXA 5 mg?

DIHEXA 5 mg is labeled at 5 mg of DIHEXA per vial. It is supplied as a lyophilized powder in a 2 mL vial, requiring reconstitution before laboratory use.

Is DIHEXA 5 mg lab tested?

This product page does not include a published laboratory report for the current batch. Independent testing of commercial DIHEXA samples has found significant purity issues, with 9 of 12 samples below 95% purity . For researchers requiring batch-specific testing documentation, please contact customer support.

Does DIHEXA cause cancer?

This is not known. DIHEXA activates the HGF/c-Met pathway, which is implicated in cancer progression when overactive . The FDA has approved drugs specifically to block c-Met for cancer treatment. A compound that stimulates this pathway with no long-term safety data raises a legitimate theoretical concern that has not been studied . No human or animal long-term safety data exists to answer this question .

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