Prostamax
Not FDA approvedSynthetic tetrapeptide bioregulator
Very thin human evidence
- Regulatory standing. Sold as a research chemical, not approved
- Animal / preclinical only. Evidence is largely animal or in-vitro
- No registered human trials. Nothing registered on ClinicalTrials.gov
- 1 cited source. Includes primary / regulatory sources
Computed with the same four public criteria as every profile. The human-evidence grade on an indexed profile is set automatically and may change when it is hand-reviewed. It is not a safety score, not a purity rating, and not medical advice, and not a claim that this compound treats, cures, or prevents any condition.
What it is
Prostamax is a short synthetic peptide, reported as the tetrapeptide Lys-Glu-Asp-Pro, developed in Russia as one of the so-called Khavinson bioregulator peptides. It is described as being modeled on peptides from prostate tissue and is proposed to influence gene expression and chromatin in aging cells, though this mechanism is not well established.
What the evidence shows
There are no registered human trials, and the roughly five published papers are mostly cell and animal studies from a small group of researchers. Any benefit for prostate health or aging in humans is unproven.
Key facts
Registered human trials
Live from ClinicalTrials.gov, refreshed daily.
Published literature
Live from Europe PMC. This is how much has been published, not how much is proven in humans.
Effects of short peptides on lymphocyte chromatin in senile subjects.
[Deheterochromatinization of the chromatin in old age induced by oligopeptide bioregulator (Lys-Glu-Asp-Pro)].
Microcalorimetric study of human blood lymphocytes culture at presence of copper, cadmium and prostamax.
[The tissue-specific effect of synthetic peptides-biologic regulators in organotypic tissues culture in young and old rats].
Sources
- PubChem compound record (CID 9848296)
- Registered trials on ClinicalTrials.gov
- Published papers on Europe PMC
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