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

CrystagenvsMelanotan-II

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
BPhase 1HUMAN-REVIEWED9/43 cited
Crystagen
Khavinson Bioregulator · Immune-Thymic
B-cellPrimary targetСhervyakova 2014
SpleenTissue specificityСhervyakova 2014
AnimalEvidence level
SQ · Protocol variable
Melanotan-II
MC1R + MC4R agonist · Tanning + sexual response
0.25–1.0 mgPer doseDorr 1996
Phase 1Evidence levelDorr 1996
~1 hrHalf-life
SQ · Abdomen · Loading 5–7 days, then maintenance

01Mechanism of Action

Parameter
Crystagen
Melanotan-II
Primary target
B-lymphocytes in splenic tissueСhervyakova 2014
MC1R (skin) + MC3R + MC4R (CNS sexual / appetite)Dorr 1996
Pathway
B-cell activation → Immune modulation during agingСhervyakova 2014
MC1R agonism → melanocyte tyrosinase → eumelanin synthesis. MC4R → autonomic sexual arousal centresDorr 1996Simerly 2023
Downstream effect
B-cell activation via apoptosis reduction; no observed increase in splenic cell renewalСhervyakova 2014
Skin darkening, photo-protection, increased sexual desire / spontaneous erectionDorr 1996
Feedback intact?
Unknown — bioregulator mechanism not fully characterized
Origin
Synthetic Lys-Glu-Asp-Gly tetrapeptide — Khavinson bioregulator series
Cyclic 7-AA modified α-MSH analog; designed at University of ArizonaDorr 1996
Antibody development

02Dosage Protocols

Parameter
Crystagen
Melanotan-II
Standard dose
Not standardized — variable protocols
Russian bioregulator literature does not specify unified human dosing.
Evidence basis
Animal / mechanistic
Phase 1 + anecdotalDorr 1996
Route
Subcutaneous (presumed from bioregulator class)
Frequency
Unknown — bioregulator protocols variable
Daily during loading; 1–2× per week maintenance
Duration
Unknown — chronic administration presumed in animal models
8–12 weeks per cycle
Half-life
Not reported
~1 hour plasma; effects on melanocytes persist days
Loading phase
0.25–0.5 mg/day SQ × 5–7 daysDorr 1996
Builds up to visible tan.
Maintenance
0.5–1.0 mg 1–2×/week
After visible tan develops; supports with UV exposure.
Lower / starter dose
0.1 mg / day
Conservative starter — assess tolerability for nausea.
Reconstitution
Bacteriostatic water; protect from light
Timing
Evening preferred (24h tan-development cycle)

04Side Effects & Safety

Parameter
Crystagen
Melanotan-II
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
Nausea
Common, especially loading phase
Flushing
Common transient
Spontaneous erection
Common in men — MC4R cross-effectDorr 1996
Increased mole / freckle pigmentation
Existing moles darken; new lesions possible
Melanoma risk
Theoretical concern — increased melanocyte activity; CAUTION in melanoma history
Appetite suppression
MC4R-mediated; mild
Pregnancy / OB
Contraindicated
Absolute Contraindications
Crystagen
  • ·Active autoimmune disease (theoretical)
Melanotan-II
  • ·History of melanoma or atypical mole syndrome
  • ·Pregnancy / breastfeeding
  • ·Active uncontrolled hypertension
Relative Contraindications
Crystagen
  • ·Pregnancy / lactation (no data)
  • ·Active B-cell malignancies
Melanotan-II
  • ·Significant freckling / dysplastic nevus
  • ·Personal or family melanoma history

05Administration Protocol

Parameter
Crystagen
Melanotan-II
1. Route
Subcutaneous injection — presumed from bioregulator class convention. Specific anatomical sites not standardized.
Add 2 mL bacteriostatic water to 10 mg vial → 5 mg/mL = 500 mcg per 0.1 mL. Light-protected.
2. Reconstitution
Protocol not standardized. If lyophilized, sterile water or bacteriostatic saline typical for peptide bioregulators.
SQ — abdomen. Rotate sites.
3. Timing
Not specified. Bioregulator protocols vary — some practitioners advocate evening dosing, others morning.
Evening preferred. UV exposure (sunlight or tanning bed) helps develop tan.
4. Storage
Lyophilized: room temperature, light-protected. Reconstituted: refrigerate, use within days to weeks depending on preservative.
Lyophilised: refrigerate, light-protected. Reconstituted: refrigerate ≤30 days.
5. Needle
29–31G 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)
Melanotan-II
— no documented stacks