Peptide
Dihexa (PNB-0408)
Dihexa (N-hexanoic-Tyr-Ile-(6) aminohexanoic amide) is an angiotensin IV-derived peptide that potentiates hepatocyte growth factor (HGF)/c-Met receptor signaling. Preclinical studies show remarkable cognitive enhancement at picomolar concentrations. In Alzheimer's disease mouse models, dihexa restored cognitive function and promoted synaptogenesis. Seven orders of magnitude more potent than BDNF in promoting dendritic spine formation. Currently investigational with no completed human clinical trials.
- Updated
- How we grade
- 7 studies cited
Research notice. This page is for education and research. Peptides may not be FDA-approved for human use and may only be legally available for research. Talk to a qualified clinician before considering any peptide.
- Best evidence
- Grade C
- Conditions studied
- 1
- Outcomes
- 4
- Graded outcomes
- 0031
Evidence by condition
- Strong
- Moderate
- Limited
- Very limited
General
| Grade | Outcome | Effect | Size | Studies | People | Studies list |
|---|---|---|---|---|---|---|
| Lipid Profile 2 preclinical studies support this finding. Primarily preclinical evidence. | Improves (the measure goes down) | Small effect | 2 studies | |||
Key findings
- Cognitive EnhancementImproves (the measure goes up)
- NeuroprotectionImproves (the measure goes up)
- SynaptogenesisImproves (the measure goes up)
Studies cited
7 studies from PubMed
- Efficiently generate functional hepatic cells from human pluripotent stem cells by complete small-molecule strategy.
- Cognitive benefits of angiotensin IV and angiotensin-(1-7): A systematic review of experimental studies.
- Small-Molecule-Directed Hepatocyte-Like Cell Differentiation of Human Pluripotent Stem Cells.
- Hepatocyte growth factor mimetic protects lateral line hair cells from aminoglycoside exposure.
- Small-molecule-driven hepatocyte differentiation of human pluripotent stem cells.
- Effect of structure on the interactions between five natural antimicrobial compounds and phospholipids of bacterial cell membrane on model monolayers.
- Phase segregation of polymerizable lipids to construct filters for separating lipid-membrane-embedded species.