PeptideTrace
Research CompoundKhavinson Bioregulator Dipeptide (Unregulated)

Vilon

KE Dipeptide, Lys-Glu

C

Evidence Grade C — Moderate human evidence. 62 published studies, 20 human. 0 registered clinical trials.

62 studiesUSEUCA

Overview

Vilon is a dipeptide (just two amino acids) from the Khavinson bioregulator programme, originally derived from thymus extract. It is the smallest peptide in the Khavinson programme, which raises fundamental questions about whether a molecule this small can exert the specific gene-regulatory effects proposed. No controlled human clinical trials have been conducted. It has no regulatory approval.

Research Activity

62studies
Human 20
Animal 40
In-vitro 6
Reviews 2

62 published studies: 20 human, 40 animal, 6 in-vitro, 2 reviews

Regulatory Status

US
Not approved by FDA(FDA)
EU
Not authorised by EMA(EMA)
CA
Not approved by Health Canada(Health Canada)

Legal Status

USNot applicable (not approved)
EUNot applicable (not authorised)
CANot applicable (not approved)

Summary

Vilon has no marketing authorisation from any major regulatory agency. No controlled human clinical trials have been conducted. Animal lifespan studies in mice reported by the Khavinson group form the evidence base.

As the smallest member of the Khavinson bioregulator peptide programme (just two amino acids), Vilon raises fundamental questions about whether a dipeptide can exert the specific gene-regulatory effects proposed. Products available through unregulated channels lack pharmaceutical quality assurance.

Mechanism of Action

Research from the Khavinson group proposes that Vilon may reverse age-related changes in chromatin structure. These proposals are part of the bioregulation theoretical framework, which posits that short peptides can modulate gene expression by interacting with DNA. These mechanisms have not been independently validated.

Research Summary

Research from the Khavinson group reports lifespan extension and tumour suppression in mouse studies, with consistent findings spanning 30+ years. However, the research is predominantly from Russian laboratories with limited methodology descriptions by Western standards. The fundamental question of how a two-amino-acid peptide could achieve sequence-specific DNA recognition — the proposed mechanism — remains scientifically debated. No large, properly controlled, double-blind trials meeting Western standards exist. No pharmacokinetic studies have been published. Products from unregulated channels lack pharmaceutical quality assurance.

Clinical Trials

No trials registered on ClinicalTrials.gov for this compound.

The information on this page is provided for educational and research reference purposes only. This is not medical advice. Always consult a qualified healthcare professional before making any health-related decisions.

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