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Peptide Database

Goals
Fat LossMuscle BuildingInjury HealingAnti-AgingCognitive EnhancementSleep OptimizationImmune SupportGut HealingSkin RejuvenationSexual Health
Peptides
Adipotide
Weight Management
AOD-9604
Weight Management
BPC-157
Healing & Recovery
Cagrilintide
Weight Management
CJC-1295
Growth Hormone
DSIP
Sleep & Recovery
Epithalon
Anti-Aging
GHK-Cu
Anti-Aging
GHRP-2
Growth Hormone
HCG
Hormone Support
Hexarelin
Growth Hormone
HGH
Growth Hormone
IGF-1 LR3
Growth Hormone
Kisspeptin
Hormone Support
Melanotan-2
Cosmetic
MOTS-C
Metabolic
NAD+
Anti-Aging
Oxytocin Acetate
Hormone Support
PEG-MGF
Recovery
PNC-27
Cancer Research
PT-141
Sexual Health
Retatrutide
Weight Management
Selank
Cognitive
Semaglutide
Weight Management
Semax
Cognitive
Sermorelin
Growth Hormone
Snap-8
Cosmetic
SS-31
Mitochondrial
TB-500
Healing & Recovery
Tesamorelin
Growth Hormone
Thymosin Alpha-1
Immune
Tirzepatide
Weight Management
Total Peptides: 32
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Peptide Comparison

VilonvsLL-37

Immunomodulatory dipeptide bioregulator (Lys-Glu) that upregulates SIRT1 expression 6-fold through direct DNA promoter binding, activates T-cell differentiation via sphingomyelin signaling, and reduces pro-inflammatory cytokines by up to 6-fold as a natural inducer of TNF tolerance

Human cathelicidin-derived antimicrobial peptide (37 amino acids) that disrupts bacterial membranes at MIC 0.62 μM against S. aureus, neutralizes endotoxin (LPS) to prevent septic shock, and has reached Phase II clinical trials as Ropocamptide for wound healing — achieving 6-fold accelerated healing at 0.5 mg/mL in venous leg ulcers

ImmuneImmune

At a Glance

Quick
comparison

Dose Range

Vilon

5–10 mg

LL-37

0.5–1.6 mg/mL (topical)

Frequency

Vilon

Once daily

LL-37

Once daily

Administration

Vilon

Subcutaneous injection

LL-37

Topical application (wound healing)

Cycle Length

Vilon

12+ weeks

LL-37

12+ weeks

Onset Speed

Vilon

Gradual (3-4 weeks)

LL-37

Moderate (1-2 weeks)

Evidence Level

Vilon

Limited human trials

LL-37

Moderate human trials (Phase 1-2)

Efficacy

Benefit
ratings

Vilon
LL-37

Anti-aging

Vilon82%
LL-370%

Inflammation

Vilon91%
LL-370%

Immune

Vilon85%
LL-3785%

Healing

Vilon0%
LL-3792%

Technical Data

Compound
specifications

Vilon

Molecular Formula

C11H21N3O5

Molecular Weight

275.3 g/mol

Half-Life

Short plasma half-life typical of dipeptides (minutes); biological effects persist for weeks to months through epigenetic modifications to SIRT1/PARP gene expression; metabolized to constituent amino acids

Bioavailability

Absorbed via intestinal peptide transporters (PepT1) when administered orally (demonstrated in animal studies); rapid absorption from subcutaneous injection sites; efficient cellular uptake and nuclear penetration due to ultra-short dipeptide structure

CAS Number

45234-02-4

LL-37

Molecular Formula

C205H340N60O53

Molecular Weight

4,493.26 Da

Half-Life

Short systemic half-life (minutes) due to protease susceptibility; local tissue persistence at wound sites is longer due to binding to extracellular matrix components and lipid membranes

Bioavailability

Topical application achieves high local wound-bed concentrations; systemic bioavailability limited by rapid proteolytic degradation and serum protein binding; not intended for oral delivery

CAS Number

154947-66-7

Protocols

Dosing
tiers

Vilon

starting

200-500 mcg subcutaneously once daily

Once daily

5 days initial assessment

Begin with the conservative research protocol. Reconstitute lyophilized Vilon in bacteriostatic water or physiological saline. Administer subcutaneously, rotating injection sites. This ultra-short dipeptide is rapidly absorbed. Effects are gradual — immune and epigenetic changes build over the treatment course. Monitor for any injection site reactions.

standard

5 mg subcutaneously once daily

Once daily

5-10 days per treatment course

Standard clinical protocol used in Russian bioregulator therapy. Administer subcutaneously once daily for 5-10 consecutive days. Repeat courses every 3-6 months for sustained immune and geroprotective benefits. Can be combined with Epithalon for comprehensive anti-aging or with Vladonix for enhanced immune support. The SIRT1 upregulation and PARP downregulation initiated during treatment persist beyond the active course.

advanced

10 mg subcutaneously once daily

Once daily

10-12 days per course

Extended protocol for individuals with significant immune compromise or advanced age. Used in clinical studies as adjuvant therapy for cancer patients alongside radio/chemotherapy. Often combined with complementary bioregulators: Thymalin for full-spectrum thymic support, Epithalon for pineal/melatonin function, and Cerluten for neuroprotection. Repeat courses every 3-6 months. Medical supervision recommended for advanced protocols.

LL-37

starting

0.5 mg/mL topical application

Once daily or every other day

2-4 weeks initial assessment

Apply LL-37 solution directly to wound bed after gentle cleansing. Cover with appropriate wound dressing. This concentration demonstrated the strongest efficacy in Phase I/IIa clinical trials for venous leg ulcers, with a 6-fold healing rate increase over placebo. Begin with every-other-day application to assess local tolerability before advancing to daily use.

standard

0.8 mg/mL topical application

Once daily

4-8 weeks

Standard clinical protocol based on Phase I/IIa dose-finding results. Apply to wound bed daily after cleansing, using sterile application technique. The peptide provides both antimicrobial clearance of wound bioburden and pro-healing effects through FPRL1-mediated angiogenesis and keratinocyte migration. Monitor wound healing progression weekly with photographic documentation.

advanced

1.6 mg/mL topical application

Once daily

8-12 weeks

Highest concentration tested in Phase I/IIa trials. Well-tolerated with no serious adverse events at this dose. Reserved for refractory wounds that have not responded to lower concentrations. The higher concentration provides enhanced antimicrobial activity and anti-biofilm effect for heavily colonized or biofilm-associated wounds. Clinical supervision recommended for extended treatment courses.

Applications

Best
suited for

Vilon

Immune system restoration in aging individuals with declining thymic function

Vilon is particularly well-suited for individuals focused on immune system restoration in aging individuals with declining thymic function. Research and clinical experience suggest meaningful benefits in this area when used as part of a comprehensive treatment approach.

Adjunctive immunomodulatory support during cancer treatment protocols

Vilon is particularly well-suited for individuals focused on adjunctive immunomodulatory support during cancer treatment protocols. Research and clinical experience suggest meaningful benefits in this area when used as part of a comprehensive treatment approach.

Geroprotective therapy targeting SIRT1/PARP pathways for cellular longevity

Vilon is particularly well-suited for individuals focused on geroprotective therapy targeting sirt1/parp pathways for cellular longevity. Research and clinical experience suggest meaningful benefits in this area when used as part of a comprehensive treatment approach.

Comprehensive Khavinson bioregulator protocols for anti-aging and immune support

Vilon is particularly well-suited for individuals focused on comprehensive khavinson bioregulator protocols for anti-aging and immune support. Research and clinical experience suggest meaningful benefits in this area when used as part of a comprehensive treatment approach.

LL-37

Treatment of chronic non-healing wounds including venous leg ulcers and diabetic ulcers

LL-37 is particularly well-suited for individuals focused on treatment of chronic non-healing wounds including venous leg ulcers and diabetic ulcers. Research and clinical experience suggest meaningful benefits in this area when used as part of a comprehensive treatment approach.

Immune defense against antibiotic-resistant bacterial infections (MRSA, Pseudomonas)

LL-37 is particularly well-suited for individuals focused on immune defense against antibiotic-resistant bacterial infections (mrsa, pseudomonas). Research and clinical experience suggest meaningful benefits in this area when used as part of a comprehensive treatment approach.

Anti-biofilm strategies for chronic wound infections and medical device-associated infections

LL-37 is particularly well-suited for individuals focused on anti-biofilm strategies for chronic wound infections and medical device-associated infections. Research and clinical experience suggest meaningful benefits in this area when used as part of a comprehensive treatment approach.

Boosting innate immune defense in immunocompromised or aging individuals

LL-37 is particularly well-suited for individuals focused on boosting innate immune defense in immunocompromised or aging individuals. Research and clinical experience suggest meaningful benefits in this area when used as part of a comprehensive treatment approach.

Safety Profile

Side
effects

Vilon

Common

  • Injection site reaction
  • Mild fatigue
  • Mild headache
  • Digestive changes

Uncommon

  • Flu-like symptoms

Serious

  • No documented serious adverse effects

LL-37

Common

  • Local site irritation
  • Transient stinging or burning
  • Mild perilesional erythema
  • Increased wound exudate

Uncommon

  • Allergic contact reaction

Serious

  • Hemolytic activity at systemic concentrations

Research Status

Safety
& evidence

Vilon

Evidence Level

Limited human trials

FDA Status

Research compound

Safety Overview

Vilon (immunomodulatory thymic peptide complex from bovine thymus) demonstrates favorable safety in Russian/Eastern European medical use over 20+ years with minimal documented serious adverse events in published literature. Bovine-derived peptide preparations carry theoretical prion disease risk (variant Creutzfeldt-Jakob disease) though processing methods and regulatory standards substantially reduce this risk. Common adverse effects are mild—local injection site reactions, transient fever, or lymphadenopathy—consistent with immune system stimulation rather than toxicity.

Contraindications

  • xKnown hypersensitivity to peptide bioregulators or constituent amino acids (lysine, glutamic acid)
  • xPregnancy and breastfeeding — insufficient reproductive safety data
  • xActive autoimmune disease in flare without medical supervision
  • xOrgan transplant recipients on immunosuppression — potential interference with immunosuppressive regimens

LL-37

Evidence Level

Moderate human trials (Phase 1-2)

FDA Status

Research compound

Safety Overview

LL-37 is an endogenous cathelicidin antimicrobial peptide naturally produced by immune cells and epithelial tissues, conferring inherent biocompatibility and low toxicity at physiological concentrations. Synthetic LL-37 shows excellent safety in in vitro immune assays and animal models with no hepatotoxicity, nephrotoxicity, or genotoxicity at relevant doses. At elevated concentrations, the cationic amphipathic structure can cause hemolysis and cell membrane damage, but therapeutic doses are far below these thresholds. Injection site reactions are minimal in research applications.

Contraindications

  • xKnown hypersensitivity to cathelicidin peptides or formulation components
  • xActive hemolytic conditions — LL-37 demonstrates concentration-dependent hemolytic activity
  • xPregnancy and breastfeeding — insufficient reproductive safety data from clinical trials
  • xSevere renal impairment — peptide clearance may be altered

Decision Guide

Which is
right for you?

Choose Vilon if...

  • Immune system restoration in aging individuals with declining thymic function
  • Adjunctive immunomodulatory support during cancer treatment protocols
  • Geroprotective therapy targeting SIRT1/PARP pathways for cellular longevity
  • Comprehensive Khavinson bioregulator protocols for anti-aging and immune support

Choose LL-37 if...

  • Treatment of chronic non-healing wounds including venous leg ulcers and diabetic ulcers
  • Immune defense against antibiotic-resistant bacterial infections (MRSA, Pseudomonas)
  • Anti-biofilm strategies for chronic wound infections and medical device-associated infections
  • Boosting innate immune defense in immunocompromised or aging individuals