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Specimen Atlas of Research Peptides81 plates · MIT
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59Plate 59Reviewed 2026-04-27

Prostamax

Khavinson Bioregulator

also known as Lys-Glu-Asp-Pro, KEDP

Synthetic tetrapeptide (Lys-Glu-Asp-Pro) developed in the Khavinson bioregulator tradition for prostate-targeted tissue regeneration. Animal and organotypic culture data demonstrate prostatic tissue-specific stimulation, chromatin decondensation, and functional restoration in aged and BPH models. Acts as putative epigenetic regulator by deheterochromatinization, reversing age-related transcriptional silencing in target tissues.

§ I

At a glance

Active concentration
0.05 ng/mL
SCE frequency increase
2.5×
Peptide length
4 AA
Route

SQ · Protocol per Khavinson tradition

§ II

Mechanism

Edit ↗

Primary target — Chromatin in prostatic cells — pericentromeric heterochromatin regions.

Pathway — Epigenetic modulation → heterochromatin decondensation → transcriptional derepression [dzhokhadze-2012].

Downstream effect — Increased sister chromatid exchange, Ag-NOR activation, reduced C-heterochromatin condensation; tissue-specific regenerative stimulation in prostate organotypic cultures [dzhokhadze-2012][zakutski-2006].

Origin — Synthetic tetrapeptide modeled on naturally occurring protein-derived bioregulators isolated between lysine-arginine motifs in long-lived species [khavinson-2017].

§ III

Dosage

Protocols described in the cited literature; not medical advice.

Edit ↗
ParameterValue
Effective concentration (in vitro)0.05 ng/mL [zakutski-2006]Organotypic culture model; demonstrated tissue-specific stimulation.
Human clinical doseNot establishedNo published human trials; dosing extrapolated from Russian clinical tradition (not peer-reviewed).
Evidence basisAnimal / organotypic culture [zakutski-2006][dzhokhadze-2012]No randomized controlled trials in humans.
Age groups studiedYoung (3-week) and aged (18-month) rats; elderly humans (75–86 years) in vitro [zakutski-2006][dzhokhadze-2012]
DurationNot specifiedKhavinson protocols typically 10–20 days per cycle; no long-term safety data.
§ III · b

Reconstitution

A pure mass-to-volume utility. Enter what you have in the vial; the atlas computes the volume per dose. No prescription information.

Inputs
mg
mL
mcg
The calculator does pure mass-to-volume math. It does not recommend a dose. Refer to Prostamax's cited literature for protocol specifics.
Volumetric outputFig. C — reconstitution math
Volume per dose
0.100mL
10.0 units on a U-100 insulin syringe
Concentration
2500
mcg per mL
Doses per vial
20
at this dose

Evidence base: Russian-language clinical literature, primarily from the St. Petersburg Institute of Bioregulation and Gerontology (Khavinson school), 1985 onward. Not extensively peer-reviewed in Western journals.

§ V

Adverse events

Severities follow the FDA / CTCAE convention.

Edit ↗
Published adverse eventsmild
None reported in available literature
Genotoxicity signalsmoderate
Increased sister chromatid exchange (SCE) — marker of DNA recombination/repair; unclear long-term implications
Metal ion interactionsmild
Modulates Cu(II) and Cd(II) chromatin effects; unknown clinical relevance
Human safety datasevere
Absent — no published Phase 1/2/3 trials
Absolute contraindications
  • Active prostate malignancy — epigenetic modulation effects unknown in cancer
Relative contraindications
  • History of prostate cancer — theoretical concern re: transcriptional activation
  • Undiagnosed prostatic nodules or elevated PSA
§ VI

Administration

Edit ↗
  1. 01
    Route

    Subcutaneous or intramuscular — per Khavinson bioregulator tradition. No published human pharmacokinetic data.

  2. 02
    Reconstitution

    If lyophilised: reconstitute with sterile water per manufacturer protocol (not standardized in literature).

  3. 03
    Frequency

    Typically daily or every-other-day in Russian clinical tradition; duration 10–20 days per cycle.

  4. 04
    Monitoring

    No established biomarkers. Theoretical: PSA, prostate imaging, symptom scores (IPSS for BPH).

  5. 05
    Note

    All protocols derived from non-peer-reviewed Russian clinical practice; Western regulatory approval absent.

Appendix

Sources

29%

of 38 rendered claims carry a resolvable citation.

  1. [dzhokhadze-2012]
    Dzhokhadze 2012[Deheterochromatinization of the chromatin in old age induced by oligopeptide bioregulator (Lys-Glu-Asp-Pro)].
    journal, 2012
  2. [khavinson-2017]
    Khavinson 2017Peptides (Epigenetic Regulators) in the Structure of Rodents with a Long and Short Lifespan.
    journal, 2017
  3. [kiladze-2009]
    Kiladze 2009Microcalorimetric study of human blood lymphocytes culture at presence of copper, cadmium and prostamax.
    journal, 2009
  4. [zakutski-2006]
    Zakutskiĭ 2006[The tissue-specific effect of synthetic peptides-biologic regulators in organotypic tissues culture in young and old rats].
    journal, 2006
Plate composed 2026-04-27 · maturity human-reviewed · schema v1 · 27 fields uncited — open contributions