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Bioregulator research · RESEARCH PROFILE

Vilon

A dipeptide discussed in immune-cell and gene-expression research.

1 specification·12 source documents·Source updated Jul 13, 2026

At a glance

A dipeptide discussed in immune-cell and gene-expression research.

This profile separates the compound’s scientific background from specification-specific preparation and source schedules. Begin with the research findings and limitations, then select the formulation you want to examine.

How it works

Vilon is associated with the Lys-Glu sequence. Research examines cellular markers and inflammatory signaling rather than a single established clinical target.[4][1][2]

Potential benefits & side effects

Interpret each outcome in the context of the study population, formulation and evidence type. Research findings do not establish a personal treatment outcome.

Potential benefits & research findings

The source describes experimental immune and tissue findings. Pulsed research schedules borrowed from related peptides require particular caution when interpreting their relevance.[1][2][3]

Read the original publications to see the measured endpoints, comparator, duration and uncertainty. Mechanistic plausibility and a favorable experimental result are different from demonstrated clinical benefit.

Side effects & evidence limitations

Interpret the reported adverse effects together with the study population, route and observation period. Small or short studies can miss uncommon and delayed harms. Evidence from a related compound does not establish the safety of Vilon.

Source-reported adverse effects and cautions

  • May modulate inflammatory cytokines such as TGF‑β1 under experimental renal stress conditions[3].
  • Early mouse studies suggest potential effects on tumor growth inhibition and lifespan extension, though human data remain limited[6].
  • Generally well tolerated in preclinical settings; occasional mild injection‑site reactions (redness/itch) may occur with subcutaneous administration.
  • Sources are available for independent reading. Individual claims and research schedules have not yet undergone an independent clinical review by Pep Science.

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    SPECIFICATIONS & SOURCE SCHEDULES

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    Select the exact formulation. Vial content, target dose and prepared concentration are different measurements.

    Showing 20 mg · 1 source tables

    Source-derived research information. Table phases retain the source’s actual duration; open-ended phases are not converted into a fixed eight-week course. Review the original study before interpreting a schedule.

    Standard / Gradual Approach (3 mL = ~6.67 mg/mL)

    Phase / CycleDaily Dose (mcg)Units (per injection) (mL)
    Cycle 1, Day 167 mcg (0.067 mg)1 unit (0.01 mL)
    Cycle 1, Day 2133 mcg (0.133 mg)2 units (0.02 mL)
    Cycle 1, Day 3200 mcg (0.20 mg)3 units (0.03 mL)
    Cycle 1, Day 4267 mcg (0.267 mg)4 units (0.04 mL)
    Cycle 1, Day 5333 mcg (0.33 mg)5 units (0.05 mL)
    Cycle 2+ (Days 1–5)333–667 mcg (0.33–0.67 mg)5–10 units (0.05–0.10 mL)

    Schedule: Inject once daily subcutaneously for 5 consecutive days, then rest for the remainder of a 4‑week cycle. Repeat monthly[4][5]. For ≤10‑unit (≤0.10 mL) administrations, consider 30‑ or 50‑unit insulin syringes for improved readability.

    Additional schedule context & duration

    Concise summary of the pulsed regimen.

    • Goal: Support immune modulation and thymic function markers based on preclinical observations[1][2].
    • Schedule: 5 consecutive days of subcutaneous injections per 4‑week cycle; repeat for 2–4 cycles.
    • Dose Range: 67–667 mcg daily with gradual titration during the first cycle.
    • Reconstitution: 3.0 mL per 20 mg vial (~6.67 mg/mL) for accurate low‑volume measurements.
    • Storage: Lyophilized frozen; reconstituted refrigerated; avoid repeated freeze–thaw.

    Suggested pulsed titration approach.

    • Start: 67 mcg (1 unit) on Day 1; increase by ~67 mcg (1 unit) each day during first cycle.
    • Target: 333–667 mcg (5–10 units) daily by Cycle 2 onward.
    • Frequency: Once per day (subcutaneous) for 5 consecutive days per cycle[5].
    • Cycle Length: 5 days on, ~23 days off (4‑week cycle); run 2–4 cycles.
    • Timing: Any consistent time; rotate injection sites.

    Read this source protocol ↗ · View cited documents ↓

    Preparation

    Preparation and stability depend on the formulation, diluent, container and handling. The source-specific notes below apply to the selected record.
    Reconstitution Steps
    1. Draw 3.0 mL bacteriostatic water with a sterile syringe.
    2. Inject slowly down the vial wall; avoid foaming.
    3. Gently swirl/roll until dissolved (do not shake).
    4. Label and refrigerate at 2–8 °C (35.6–46.4 °F), protected from light; use within ~1 week or aliquot and freeze[10].

    Important: This guide is for educational purposes only and is not medical advice. For research use only. Not for human consumption.

    Storage Instructions

    Proper storage preserves peptide quality.

    • Lyophilized: Store at −20 °C (−4 °F) short‑term or −80 °C (−112 °F) long‑term in dry, dark conditions; minimize moisture exposure[10].
    • Reconstituted: Refrigerate at 2–8 °C (35.6–46.4 °F); use within ~1 week or prepare aliquots and freeze to extend stability.
    • Allow vials to reach room temperature before opening to reduce condensation uptake.

    Injection Technique

    General subcutaneous guidance from clinical best‑practice resources[9].

    • Clean the vial stopper and skin with alcohol; allow to dry.
    • Pinch a skinfold; insert the needle at 45–90° into subcutaneous tissue[7][8].
    • Do not aspirate for subcutaneous injections; inject slowly and steadily[9].
    • Rotate sites systematically (abdomen, thighs, upper arms) to avoid lipohypertrophy[9].

    Materials & quantity planning

    Source materials checklist · 20 mg

    Plan based on an 8–16 week pulsed protocol (5 injection days per 4‑week cycle).

    • Peptide Vials (Vilon, 20 mg each):

      • 8 weeks (2 cycles, 10 injections) ≈ 1 vial
      • 12 weeks (3 cycles, 15 injections) ≈ 1 vial
      • 16 weeks (4 cycles, 20 injections) ≈ 1 vial
    • Insulin Syringes (U‑100, 30‑ or 50‑unit preferred):

      • Per cycle: 5 syringes (1/day × 5 days)
      • 8 weeks: 10 syringes
      • 12 weeks: 15 syringes
      • 16 weeks: 20 syringes
    • Bacteriostatic Water (10 mL bottles): Use 3.0 mL per vial for reconstitution.

      • 8–16 weeks (1 vial): 3 mL1 × 10 mL bottle
    • Alcohol Swabs: One for the vial stopper + one for the injection site each day.

      • Per cycle: 10 swabs (2/day × 5 days)
      • 8 weeks: 20 swabs
      • 12 weeks: 30 swabs
      • 16 weeks: 40 swabs → recommend 1 × 100‑count box


    Calculate a phased quantity

    Enter each finite phase from the schedule you are studying. Open-ended phases need an explicit duration. Calculation uses 20 mg per vial and 3 mL per vial.

    Complete each phase to calculate totals.

    Quantity estimates exclude preparation losses and expiry. Follow the formulation’s handling and disposal requirements.

    FOLLOW THE EVIDENCE

    References & further reading

    Original publications and source documents cited across this product’s variants. A listed source is not an independent endorsement of a dosing schedule.

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    Related topics are not interchangeable compounds or formulations.