Dihexa 5MG

Dihexa 5MG

Dihexa 5MG

Dihexa 5MG

Dihexa (PNB-0408 / N-hexanoic-Tyr-Ile-(6)-aminohexanoic amide) is a blood-brain barrier permeable oligopeptide analog derived from Angiotensin IV. Operating as a high-affinity positive allosteric modulator of Hepatocyte Growth Factor (HGF), Dihexa binds HGF to potentiate c-Met receptor tyrosine kinase signaling. This cascade stimulates robust dendritic spinogenesis and new functional synaptogenesis in neuronal models, demonstrating neurotrophic potency up to seven orders of magnitude greater than Brain-Derived Neurotrophic Factor (BDNF).

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Certificate of Analysis

What is Dihexa?

Dihexa (known chemically as PNB-0408, N-hexanoic-Tyr-Ile-(6)-aminohexanoic amide, or Hexanoyl-Tyr-Ile-Ahx-NH2) is a synthetic oligopeptide derived from Nle1-Angiotensin IV. Originally engineered at Washington State University as a blood-brain barrier permeable procognitive agent, Dihexa binds with ultra-high affinity to Hepatocyte Growth Factor (HGF).

Batch-verified for purity at Modern Aminos, Dihexa is supplied as a high-purity lyophilized reference powder for laboratory screening and synaptic plasticity assays. Researchers studying neurodegenerative recovery, dendritic arborization, and growth factor receptor kinetics utilize Dihexa to evaluate c-Met activation alongside related neurotrophic and glutamatergic reference standards available on the site, such as P21, TAK-653, and Noopept.

Chemical and Molecular Data

Compound Name Dihexa (PNB-0408)
Format & Packaging Analytical-Grade Lyophilized Reference Powder
Synonyms / Alt Names PNB-0408, N-hexanoic-Tyr-Ile-(6)-aminohexanoic amide, Hexanoyl-Tyr-Ile-Ahx-NH2
CAS Number 1401708-83-5
Chemical Formula C27H44N4O5
Molecular Weight 504.67 g/mol
IUPAC Name 6-[(2S,3S)-2-[(2S)-2-hexanamido-3-(4-hydroxyphenyl)propanamido]-3-methylpentanamido]hexanamide
InChIKey XEUVNVNAVKZSPT-JTJYXVOQSA-N
SMILES Code CCCCCC(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H]([C@@H](C)CC)C(=O)NCCCCCC(N)=O

What are the Mechanisms of Action?

The biochemical pathways and cellular targets of Dihexa in laboratory research include:

  • Hepatocyte Growth Factor (HGF) Dimerization & c-Met Activation: Research demonstrates that Dihexa binds directly to HGF with picomolar affinity. This binding facilitates HGF dimerization and potentiates auto-phosphorylation of the c-Met receptor tyrosine kinase, initiating downstream intracellular survival and morphogenesis signals.
  • Dendritic Spinogenesis & Functional Synaptogenesis: Upon c-Met activation in hippocampal and cortical neurons, Dihexa triggers rapid actin cytoskeletal remodeling. This drives the outgrowth of new dendritic spines and accelerates the formation of functional post-synaptic connections between adjacent neurons.
  • Neurotrophic Signaling Amplification: In comparative neurotrophic cell culture assays, Dihexa-mediated HGF/c-Met activation demonstrated a capacity to stimulate dendritic arborization up to seven orders of magnitude more potently than Brain-Derived Neurotrophic Factor (BDNF), maintaining cellular viability during neurotoxic insults.

What do Preclinical & Academic Studies Show for Dihexa?

When evaluating research efficacy and published scientific literature for Dihexa (PNB-0408):

  • Procognitive & Synaptogenic HGF/c-Met Mechanism (PMC): Landmark preclinical trials archived in PMC (PMC4201273) confirm that Dihexa crosses biological membranes to induce c-Met phosphorylation in the presence of subthreshold HGF levels. Neuronal cultures exhibited marked expansion in hippocampal spinogenesis and functional synapse density.
  • HGF/c-Met Target Validation in Neurodegenerative Models (PubMed): Peer-reviewed research cataloged on PubMed (PMID: 25649658) details how activating the brain HGF/c-Met system mitigates cognitive deficits in animal models of Alzheimer’s disease-like pathology, promoting stem cell differentiation, neurogenesis, and tissue protection.
  • Chemical Profiling & Structure Verification (PubChem): Structural data and mass spectrometry profiles maintained on PubChem document the lipophilicity parameters, peptide sequence integrity, and solid-state stability of Dihexa as an Angiotensin IV-derived research oligopeptide.

How does Dihexa compare to other compounds?

To evaluate receptor targeting, synaptogenic potency, and neurotrophic pathways, researchers compare Dihexa against alternative cognitive and neuro-regenerative reference compounds available at Modern Aminos:

Compound / Reference Primary Target & Class Core Mechanism of Action Research Profile & Focus
Dihexa (PNB-0408) Angiotensin IV Derived Oligopeptide / HGF Potentiator Binds HGF to drive c-Met receptor dimerization, spinogenesis, and functional synaptogenesis Ultra-potent synaptogenic compound engineered for structural neural repair, new synapse formation, and HGF pathway research
P21 CNTF-Derived Synthetic Peptide Mimetic Promotes neurogenesis and dendritic arborization via Ciliary Neurotrophic Factor (CNTF) / JAK-STAT signaling Focuses on neurotrophic factor stimulation and neural stem cell differentiation without direct HGF/c-Met receptor binding
TAK-653 AMPA Receptor Selective Positive Allosteric Modulator (PAM) Potentiates postsynaptic AMPA currents to activate ERK/mTORC1 pathways and drive BDNF synthesis Focuses on glutamatergic signaling, activity-dependent neuroplasticity, and rapid-onset synaptic potentiation
Noopept Dipeptide-Derived Nootropic & HIF-1 Modulator Sensitizes central AMPA/NMDA receptors and upregulates hippocampal BDNF and NGF expression Classic cognitive research compound focused on long-term potentiation, sensory processing, and neuroprotective signaling

Frequently Asked Questions (FAQs)

1. Is Modern Aminos a reliable place to buy Dihexa?

Yes, Modern Aminos is a trusted supplier of high-purity research chemicals and reference peptides. Every batch of Dihexa undergoes rigorous third-party analytical testing (including HPLC and Mass Spectrometry) to verify minimum 99%+ purity, exact molecular weight (504.67 g/mol), and complete absence of unreacted synthetic fragments or heavy metals.

2. What is the molecular target of Dihexa?

Dihexa targets Hepatocyte Growth Factor (HGF). It binds HGF with high affinity, facilitating its interaction with the c-Met receptor tyrosine kinase. Activation of c-Met initiates downstream intracellular cascades that govern cell survival, motogenesis, and dendritic spinogenesis.

3. How does Dihexa’s neurotrophic potency compare to BDNF in cell assays?

In preclinical cell culture assays measuring dendritic arborization and synaptic outgrowth, Dihexa demonstrated neurotrophic activity estimated to be up to seven orders of magnitude 1,000,000 times more potent than Brain-Derived Neurotrophic Factor (BDNF) on a molar basis.

4. What is spinogenesis and why is it significant in Dihexa research?

Spinogenesis is the biological process by which neurons sprout new dendritic spines—the physical protrusions that receive synaptic inputs. Dihexa’s ability to drive spinogenesis allows researchers to study structural neural regeneration and the restoration of lost synaptic connections in damaged brain tissue models.

5. How should lyophilized Dihexa powder be reconstituted for laboratory use?

Lyophilized Dihexa reference powder dissolves readily in organic solvents such as dimethyl sulfoxide (DMSO) or ethanol. For biological assays, stock solutions prepared in DMSO can be diluted into sterile laboratory buffers or culture media immediately prior to application.

6. How does Dihexa differ structurally and mechanically from P21?

Dihexa is an N-hexanoylated tripeptide derived from Angiotensin IV that acts through HGF/c-Met receptor activation. P21 is an adamantane-containing synthetic peptide mimetic derived from Ciliary Neurotrophic Factor (CNTF) that operates via CNTF/JAK-STAT pathways. While both promote neural repair, they engage entirely different growth factor systems.

7. Is Dihexa stable and permeable across biological membrane barriers?

Yes. The N-terminal hexanoyl cap and specific hydrophobic amino acid sequence (Tyr-Ile-Ahx) were engineered specifically to increase lipophilicity and metabolic stability, allowing Dihexa to cross cell membranes and the blood-brain barrier intact in preclinical models.

8. What are the proper storage and research handling parameters for Dihexa?

Lyophilized Dihexa powder should be stored sealed in its original reagent vial at -20°C for long-term preservation. Protect from moisture, heat, and direct light exposure. Reconstituted liquid stock solutions in DMSO should be aliquoted and stored frozen to maintain chemical stability.

Disclaimer: All compounds and research materials provided by Modern Aminos are strictly for laboratory and research professional use only. They are not approved for human or animal use nor consumption by the Food and Drug Administration (FDA). These products should not be used for any form of in vivo experimentation or for any other non-laboratory purpose. Any violation or indication of human or animal use will result in immediate removal from being able to purchase products in the future. By purchasing these products, you acknowledge that they will be used exclusively within a controlled and qualified research environment.

The products offered by Modern Aminos are intended strictly for laboratory research purposes only and are sold exclusively to qualified professionals, institutions, and entities. These products are not for human consumption, veterinary use, or any other application involving living organisms, including but not limited to diagnostic, therapeutic, or recreational purposes.

By purchasing this product, you confirm that:

  • You are a qualified professional or entity with the necessary knowledge, training, and facilities to handle chemical reagents safely and appropriately.
  • You will use this product in full compliance with all applicable local, state, and federal laws and regulations.

Prohibited Uses

  • This product is not to be used as an active pharmaceutical ingredient (API) in compounding or manufacturing drugs for human or veterinary use.
  • It is strictly prohibited to use this product for administration to humans or animals under any circumstances.
  • Modern Aminos does not condone or permit the use of its products for the development, testing, or production of illegal substances.

Regulatory Compliance

Modern Aminos does not claim that this product is approved by the U.S. Food and Drug Administration (FDA) for any purpose. The statements regarding this product have not been evaluated by the FDA. This product is not intended to diagnose, treat, cure, or prevent any disease.

Liability Statement

The buyer assumes full responsibility for ensuring the safe handling, storage, and use of this product. Modern Aminos is not liable for any damages, direct or indirect, resulting from improper handling, storage, or unauthorized use of this product. Furthermore, Modern Aminos reserves the right to refuse sales to any individual or entity suspected of misusing its products.

If you have questions about the safe and lawful use of this product, consult a qualified professional with expertise in laboratory research. By proceeding with this purchase, you agree to these terms and conditions.

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