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Specimen Atlas of Research Peptides81 plates · MIT
Side-by-side · Research reference

CrystagenvsEpitalon

Side-by-side comparison across mechanism, dosage, evidence, side effects, administration, and stack synergies. Citations on every claim where available.

AAnimal-MechanisticHUMAN-REVIEWED12/40 cited
BHuman-MechanisticAUTO-DRAFTED8/37 cited
Crystagen
Khavinson Bioregulator · Immune-Thymic
B-cellPrimary targetСhervyakova 2014
SpleenTissue specificityСhervyakova 2014
AnimalEvidence level
SQ · Protocol variable
Epitalon
Pineal bioregulator · Telomerase activator
5–10 mgPer cycle doseKhavinson 2003
HumanMechanisticKhavinson 2003
HoursHalf-life (est)
SQ or IM · Abdomen · Daily for 10–20 days

01Mechanism of Action

Parameter
Crystagen
Epitalon
Primary target
B-lymphocytes in splenic tissueСhervyakova 2014
Telomerase activity (proposed); pineal melatonin axis modulationKhavinson 2003
Pathway
B-cell activation → Immune modulation during agingСhervyakova 2014
Activation of telomerase reverse transcriptase (hTERT) in somatic cells; pineal-axis modulation supports endogenous melatoninKhavinson 2003
Downstream effect
B-cell activation via apoptosis reduction; no observed increase in splenic cell renewalСhervyakova 2014
Telomere elongation, improved sleep architecture, reported lifespan extension in aged miceKhavinson 2003
Feedback intact?
Unknown — bioregulator mechanism not fully characterized
Origin
Synthetic Lys-Glu-Asp-Gly tetrapeptide — Khavinson bioregulator series
Synthetic 4-AA peptide derived from epithalamin (a natural pineal extract)Khavinson 2003
Antibody development

02Dosage Protocols

Parameter
Crystagen
Epitalon
Standard dose
Not standardized — variable protocols
Russian bioregulator literature does not specify unified human dosing.
5–10 mg / day for 10–20 days, 1–2× per yearKhavinson 2003
Anecdotal community protocol. Russian clinical literature uses similar cycling.
Evidence basis
Animal / mechanistic
In-vitro telomerase + Russian clinical trialsKhavinson 2003
Route
Subcutaneous (presumed from bioregulator class)
Frequency
Unknown — bioregulator protocols variable
Once daily during a cycle
Duration
Unknown — chronic administration presumed in animal models
10–20 day cycles, 1–2× per year
Half-life
Not reported
Hours (estimated)
Lower / starter dose
2.5 mg / day
Reconstitution
Bacteriostatic water
Timing
Pre-sleep preferred (pineal alignment)

04Side Effects & Safety

Parameter
Crystagen
Epitalon
Published adverse events
None reported in available animal literature
Human safety data
Absent — no controlled human trials identified
Autoimmune considerations
Theoretical concern with B-cell modulators in predisposed individuals
Injection site reaction
Mild irritation
Sleep architecture
Improved subjective sleep quality (anecdotal)
Cancer risk
Theoretical via telomerase activation in pre-malignant cells
Long-term safety
Limited Western RCT data
Pregnancy / OB
Avoid
Antibody formation
Not reported
Absolute Contraindications
Crystagen
  • ·Active autoimmune disease (theoretical)
Epitalon
  • ·Pregnancy / breastfeeding
  • ·Active malignancy or pre-malignant state
Relative Contraindications
Crystagen
  • ·Pregnancy / lactation (no data)
  • ·Active B-cell malignancies
Epitalon
  • ·Family history of cancer

05Administration Protocol

Parameter
Crystagen
Epitalon
1. Route
Subcutaneous injection — presumed from bioregulator class convention. Specific anatomical sites not standardized.
Add 1–2 mL bacteriostatic water to 10 mg vial → 5–10 mg/mL.
2. Reconstitution
Protocol not standardized. If lyophilized, sterile water or bacteriostatic saline typical for peptide bioregulators.
SQ — abdomen preferred. Rotate sites.
3. Timing
Not specified. Bioregulator protocols vary — some practitioners advocate evening dosing, others morning.
Pre-sleep preferred to align with pineal axis.
4. Storage
Lyophilized: room temperature, light-protected. Reconstituted: refrigerate, use within days to weeks depending on preservative.
Lyophilised: room temp, light-protected. Reconstituted: refrigerate ≤30 days.
5. Needle
29–31G, 4–8 mm insulin syringe.

06Stack Synergy

Crystagen
+ Vilon
Multi-pathway
View Vilon

Vilon (Lys-Glu) activates T-helper cells via apoptosis reduction, while Crystagen activates B-cells. Dual T/B immune modulation in aging models may provide complementary thymic-immune support within the Khavinson bioregulator framework. Both target splenic immune aging through distinct lymphocyte subsets.

Crystagen
Dose unknown · SQ
Vilon
Dose unknown · SQ
Frequency
Protocol variable
Primary benefit
Broader thymic-immune coverage (T-cell + B-cell)
Epitalon
— no documented stacks