Educational reference

Peptide library

Vilon

Your guide to this compound.

Mechanism illustrationEnlarge
Vilon: Medical scientific diagram. Open full size to read labels; evidence and limitations appear in the profile.
Educational illustration · Read the evidence and limitations below.

Evidence in perspective

Calling Vilon unidentified, or claiming only cell evidence exists, was too broad. Its sequence and a human report are documented, but biomarker findings cannot establish immune enhancement, longevity or a safe general regimen.

About this assessment

Identity sources and selected source evidence assessed; scope below.

Human report located; full Russian methods/results not obtained in this pass. Indexing as randomized does not establish low risk of bias. No treatment recommendation or clinician sign-off.

Editorial assessment · 2026-09-07

Source 1 · pubmed.ncbi.nlm.nih.gov

Source 2 · pubmed.ncbi.nlm.nih.gov

Who was studied

Patients with type 1 diabetes in a Russian report indexed as a randomized controlled trial; abstract-level assessment.

What the sources found

The report describes changes in coagulation and fibrinolysis markers with Vilon. Its abstract does not provide enough allocation, sample-size, effect-size or adverse-event detail for a reliable benefit–risk estimate.

Patients with type 1 diabetes in a Russian report indexed as a randomized controlled trial; abstract-level assessment.

Source · Abstract / selected methods and results / product description

Regulatory scope

Identity documentation and publication do not confer marketing authorization. No new jurisdiction-specific approval claim is made.

What remains unknown

Human report located; full Russian methods/results not obtained in this pass. Indexing as randomized does not establish low risk of bias. No treatment recommendation or clinician sign-off.

How it works

Identity and evidence must be read separately.

Calling Vilon unidentified, or claiming only cell evidence exists, was too broad. Its sequence and a human report are documented, but biomarker findings cannot establish immune enhancement, longevity or a safe general regimen.

Limited clinical evidence

The catalog describes a limited clinical evidence base. Small or uncontrolled studies may not separate treatment effects from chance, placebo effects or bias.

Understanding the evidence

Reported adverse effects

  • A complete human adverse-effect profile is not established by the selected sources.

Contraindications

  • No complete product-specific contraindication assessment is available; absence of a listed risk is not evidence of safety.

Limited clinical evidence

The catalog describes a limited clinical evidence base. Small or uncontrolled studies may not separate treatment effects from chance, placebo effects or bias.

Understanding the evidence

Sources used for this snapshot

Source 1 · pubmed.ncbi.nlm.nih.gov

Source 2 · pubmed.ncbi.nlm.nih.gov

Claim-by-claim evidence

Identity

Vilon is the dipeptide Lys-Glu (KE), explicitly named in animal experiments and a Russian human report.

Catalog identity only; not authentication of a purchased vial or clinical approval.

Identity / product description / methods

Findings

The report describes changes in coagulation and fibrinolysis markers with Vilon. Its abstract does not provide enough allocation, sample-size, effect-size or adverse-event detail for a reliable benefit–risk estimate.

Patients with type 1 diabetes in a Russian report indexed as a randomized controlled trial; abstract-level assessment.

Abstract / selected methods and results / product description

References

  1. Pliss et al. The effect of vilon (Lys-Glu) on dimethylhydrazine-induced neoplasia. 2005. Mouse study.

    PMID: 16308980

    Open

  2. Kuznik et al. Effect of thymomimetic vilon on coagulation and fibrinolysis in type 1 diabetes. Adv Gerontol. 2006. Russian report.

    PMID: 17152731

    Open

Catalog review date: Sep 7, 2026. This date alone does not establish independent clinical review.

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