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Vilon

Also known as: KE dipeptide, Lys-Glu, L-lysyl-L-glutamic acid

โœ“Reviewed byDr. Research Team(MD (composite credential representing medical review team), PhD in Pharmacology)
๐Ÿ“…Updated February 12, 2026
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๐Ÿ“ŒTL;DR

  • โ€ขExtended lifespan and inhibited spontaneous tumor growth in CBA mice with chronic subcutaneous administration (Khavinson group)
  • โ€ขInduced deheterochromatinization (chromatin unrolling) in aged lymphocytes, potentially reactivating silenced genes
  • โ€ขImmunomodulatory effects on thymus cell cultures, promoting immune cell differentiation
  • โ€ขRegulated expression of IGF1, FOXO1, TERT, and NFkB genes in mesenchymal stem cells in vitro
  • โ€ขExtremely small molecular size (275 Da dipeptide) enabling potential oral bioavailability
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Protocol Quick-Reference

Geroprotective and immunomodulatory research

Dosing

Amount

Not established for humans (preclinical only)

Frequency

Chronic administration in animal models

Duration

Long-term in mouse lifespan studies

Administration

Route

SC

Schedule

Chronic subcutaneous injection in preclinical models

Timing

All dosing is from preclinical mouse studies. No human pharmacokinetic data exists. Oral capsule formulations marketed in Russia lack clinical validation.

Cycle

Duration

Long-term (preclinical lifespan studies)

Repeatable

Yes

โš—๏ธ Suggested Bloodwork (2 tests)

CBC with differential

When: Baseline

Why: Baseline immune cell counts for immunomodulatory assessment

CMP (Comprehensive Metabolic Panel)

When: Baseline

Why: Liver and kidney function baseline

๐Ÿ’ก Key Considerations
  • โ†’No validated human dosing protocols exist; all research is from a single research group (Khavinson) without independent replication
  • โ†’Oral bioavailability of intact vilon dipeptide has not been demonstrated in formal pharmacokinetic studies
  • โ†’Not approved by FDA, EMA, or other Western regulatory agencies; no Western clinical trials registered

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Mechanism of action for Vilon
How Vilon works at the cellular level
Key benefits and uses of Vilon
Overview of Vilon benefits and applications
Scientific Details
Molecular Formula
C11H21N3O5
Molecular Weight
275.3 Da
Sequence
KE

What is Vilon?#

Vilon (L-lysyl-L-glutamic acid, abbreviated KE) is a synthetic dipeptide consisting of just two amino acids: lysine and glutamic acid. It was developed by Professor Vladimir Khavinson and colleagues at the St. Petersburg Institute of Bioregulation and Gerontology in Russia as part of a broader research program investigating tissue-specific peptide bioregulators.

The concept underlying vilon is that endogenous tissues produce specific short peptides that regulate gene expression and maintain cellular homeostasis. According to this theory, the thymus produces regulatory dipeptides including the KE sequence, and supplementation with synthetic vilon can restore age-related declines in thymic function and immune regulation.

Vilon has a molecular weight of approximately 275 Da, making it one of the smallest bioactive peptides studied. Its small size raises the possibility of oral bioavailability, and capsule formulations have been marketed in Russia.

Mechanism of Action#

Epigenetic Modulation#

The most studied mechanism of vilon is its proposed effect on chromatin structure. In cell cultures from aged donors, vilon has been reported to induce deheterochromatinization, the unrolling of condensed heterochromatin regions that accumulate during aging. This process may reactivate genes silenced by age-related chromatin condensation.

In human embryonic mesenchymal stem cells, vilon was reported to regulate the expression of genes including IGF1, FOXO1, TERT (telomerase reverse transcriptase), TNKS2, and NFkB. These genes are involved in growth factor signaling, longevity pathways, telomere maintenance, and inflammatory regulation.

Immunomodulation#

Vilon has been studied for effects on thymic cell cultures, where it reportedly promoted immune cell differentiation and modulated the balance between various lymphocyte subsets. The specific receptor or signaling pathway mediating these effects has not been identified.

Geroprotective Effects#

In mouse studies, chronic vilon administration was associated with increased lifespan, reduced spontaneous tumor incidence, and improved physical parameters (increased activity and endurance) without adverse effects on development or estrous function.

Research Overview#

Vilon research has been published primarily by the Khavinson group over approximately two decades. Key study categories include:

  1. Lifespan studies: Chronic SC vilon administration in CBA mice extended lifespan and reduced spontaneous tumors
  2. Chromatin studies: Vilon-induced deheterochromatinization in lymphocytes from aged human donors
  3. Gene expression: Effects on longevity-associated genes in stem cell cultures
  4. Immunomodulation: Effects on thymic cell differentiation and immune marker expression

Important Considerations#

Several significant limitations apply to vilon research:

  • Single research group: The vast majority of vilon publications originate from the Khavinson group. Independent replication by Western laboratories is largely absent.
  • Publication venues: Many key studies appear in Russian-language journals or low-impact international journals, making independent peer review assessment challenging.
  • No Western clinical trials: No clinical trials are registered with ClinicalTrials.gov or EudraCT for vilon.
  • Mechanism not defined: The specific molecular target, receptor, or signaling cascade mediating vilon's effects has not been identified.
  • Regulatory status: Not approved by FDA, EMA, or other major Western regulatory agencies.
  • Oral bioavailability: While proposed, formal pharmacokinetic studies demonstrating oral absorption of intact vilon have not been published.

Key Research Findings#

A synthetic dipeptide vilon (L-Lys-L-Glu) inhibits growth of spontaneous tumors and increases life span of mice, published in Doklady Biological Sciences (Khavinson VKh and Anisimov VN, 2000; PMID: 10944717):

Chronic subcutaneous vilon administration to female CBA mice from 6 months of age inhibited spontaneous tumor growth and extended lifespan. No adverse effects on development or reproductive function were observed.

  • Inhibited growth of spontaneous tumors in CBA mice
  • Increased lifespan of treated mice compared to controls
  • Long-term administration was safe with no adverse developmental effects

Effect of vilon on biological age and lifespan in mice, published in Bulletin of Experimental Biology and Medicine (Khavinson VKh and Anisimov VN, 2000; PMID: 11140587):

Subcutaneous vilon administration to female CBA mice from 6 months of age increased physical activity and endurance, decreased body temperature, prolonged lifespan, and prevented spontaneous neoplasm development. No effect on estrous function or free radical processes.

  • Increased physical activity and endurance in treated mice
  • Decreased body temperature (potential caloric restriction-like effect)
  • Prolonged lifespan and prevented spontaneous neoplasm development

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Community Protocols Available

See real-world usage patterns alongside the clinical evidence above. Community-sourced, not clinically verified.

Based on 15+ community reports

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Medical Disclaimer

This website is for educational and informational purposes only. The information provided is not intended to diagnose, treat, cure, or prevent any disease. Always consult with a qualified healthcare professional before using any peptide or supplement.

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