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Protocols · Immune

Vilon dosage protocol

Dosage and protocol information sourced exclusively from PeptideDosages.com.

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Dosage and protocol figures on this page are reproduced only from the matching PeptideDosages.com protocol. The 3 ml table is arithmetic based on those source amounts and the listed vial sizes. Educational research only — not instructions or medical advice.

Dosage chart

The dosage amounts and schedules below come only from PeptideDosages.com. Syringe-unit figures are mathematical conversions of those source amounts using exactly 3 ml of bacteriostatic water. Educational reference only — not instructions or medical advice.

Vilon · 20 mg Vial

Vilon is dosed at 67 mcg–667 mcg daily via subcutaneous injection in educational protocols.

Typical range
67–670 mcg once daily for 5 consecutive days per cycle.

Standard / Gradual Approach

Phase / CycleDaily Dose (mcg)
Cycle 1, Day 167 mcg (0.067 mg)
Cycle 1, Day 2133 mcg (0.133 mg)
Cycle 1, Day 3200 mcg (0.20 mg)
Cycle 1, Day 4267 mcg (0.267 mg)
Cycle 1, Day 5333 mcg (0.33 mg)
Cycle 2+ (Days 1–5)333–667 mcg (0.33–0.67 mg)

3 ml conversion

20 mg + 3 ml = 6.67 mg/ml. Choose your vial strength to update the units below.

Source doseU-100 syringe
67 mcg1.0 units
133 mcg2.0 units
200 mcg3.0 units
267 mcg4.0 units
333 mcg5.0 units
0.33 mg4.9 units
667 mcg10 units
0.67 mg10 units
Source chart on peptidedosages.com

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Vilon: research background

What the compound is

Vilon is a synthetic dipeptide, meaning it is made of two amino acids linked together. Its specific amino acid sequence is Lys-Glu (Lysine-Glutamic acid) (PMID 12209581, PMID 37042594, PMID 12360356, PMID 11140587, PMID 12420071, PMID 25826983).

How it is thought to work

Vilon, along with other short peptide bioregulators, is believed to induce selective heterochromatinization and deheterochromatinization (remodeling of facultative heterochromatin) of chromosome regions in lymphocytes from individuals aged 75-88 years. This process involves the unrolling or decondensation of total heterochromatin and satellite stalks of acrocentric chromosomes, which activates the synthetic processes of ribosomal genes (PMID 37042594). These short peptides are also known to regulate gene expression and protein synthesis (PMID 25826983). Studies using DNA-microarray technology in mice found that Vilon alone changed the expression of 36 clones (genes or DNA sequences), activating 157 clones and inhibiting 23 clones in the heart (PMID 12360356).

What laboratory and animal studies report

In female CBA mice, subcutaneous administration of Vilon starting at 6 months of age increased physical activity and endurance, decreased body temperature, prolonged lifespan, and prevented the development of spontaneous neoplasms (PMID 11140587). In aged rats, oral administration of Vilon for one month improved transport characteristics of the small intestine, specifically enhancing passive glucose accumulation in the serous fluid of the distal small intestine and stimulating active glucose accumulation in the serous sac of the medial small intestine (PMID 12420071). Vilon also demonstrated an 'oncomodulating action' in mice with transplanted Lewis lung carcinoma, increasing the survival of the mice when injected at 1 mg/kg doses (PMID 14743610). However, a different study in female FVB/N HER-2/neu transgenic mice reported that Vilon treatment (1 microg/mouse for 5 consecutive days monthly) produced significant negative effects, including an increased incidence of mammary cancer, a shorter mean latent period of tumors, and an increased cumulative number of tumors, compared to control animals. While Vilon partially reduced HER-2/neu mRNA expression in mammary tumors, it remained significantly higher than in Epitalon-treated animals (PMID 12209581). In organotypic spleen tissue cultures from young and old rats, Vilon stimulated apoptosis (programmed cell death) (PMID 14743610).

Open questions and limitations

Although Vilon has shown some positive effects in geroprotection and cancer modulation in animal models, its use in combination with cytostatic drugs like cyclophosphan resulted in decreased survival in mice, suggesting they should not be used synchronously (PMID 14743610). Furthermore, Vilon's effect on mammary cancer development in HER-2/neu transgenic mice showed concerning negative outcomes, including increased tumor incidence (PMID 12209581). These contrasting findings in different cancer models highlight the complexity of Vilon's effects. One abstract uses 'ViLoN' as an algorithm for data integration in patient stratification, which is unrelated to the Lys-Glu peptide (PMID 36395816). There are no human studies described regarding the Lys-Glu peptide Vilon's effects.

Studies cited in this section

Summarised from the PubMed abstracts listed above. Educational reference only — not medical advice or instructions.

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Peptide Intel Hub is an independent educational publication. We are not affiliated with, owned by, or the same company as Biomech Peptides and Regena.app (biomechpeptides.com / regena.app). We do not sell, supply, ship or take payment for any compound. Because readers regularly ask where compounds discussed in published studies can be sourced for laboratory work, we list Biomech Peptides and Regena.app as suppliers we have verified and trust — every batch is released with a lot-matched third-party certificate of analysis (HPLC purity and mass-spectrometry identity). Outbound links are marked nofollow/sponsored and are provided to help readers, not to sell.