Side-by-side · Research reference
GHRP-2vsMelanotan-II
Side-by-side comparison across mechanism, dosage, evidence, side effects, administration, and stack synergies. Citations on every claim where available.
APhase 2Reviewed15/42 cited
BPhase 1Reviewed9/43 cited
GHRP-2
Hexapeptide GHRP · Phase 2 (clinical diagnostic)
SQ · Multiple sites · 1–3×/day
01Mechanism of Action
Parameter
GHRP-2
Melanotan-II
Primary target
Ghrelin receptor (GHS-R1a) on anterior pituitaryBowers 1990
MC1R (skin) + MC3R + MC4R (CNS sexual / appetite)Dorr 1996
Pathway
GHS-R1a → Gαq → Ca²⁺ → GH vesicle exocytosisBowers 2002
MC1R agonism → melanocyte tyrosinase → eumelanin synthesis. MC4R → autonomic sexual arousal centresDorr 1996Simerly 2023
Downstream effect
Strong GH pulse + IGF-1 elevation; appetite increase via ghrelin agonismBowers 2002
Skin darkening, photo-protection, increased sexual desire / spontaneous erectionDorr 1996
Feedback intact?
Yes, with somatostatin feedback active
—
Origin
Synthetic hexapeptide; developed by Bowers/Tulane group in the 1980sBowers 1990
Cyclic 7-AA modified α-MSH analog; designed at University of ArizonaDorr 1996
Antibody development
—
—
02Dosage Protocols
Parameter
GHRP-2
Melanotan-II
Frequency
1–3× per day
Daily during loading; 1–2× per week maintenance
Lower / starter dose
50 mcg per dose
0.1 mg / day
Conservative starter — assess tolerability for nausea.
Duration
8–12 weeks on / 4 off (anecdotal)
8–12 weeks per cycle
Reconstitution
Bacteriostatic water
Bacteriostatic water; protect from light
Timing
Pre-sleep + fasted preferred
Evening preferred (24h tan-development cycle)
Maintenance
—
0.5–1.0 mg 1–2×/week
After visible tan develops; supports with UV exposure.
04Side Effects & Safety
Parameter
GHRP-2
Melanotan-II
Prolactin elevation
Mild but measurable
—
Hunger
Strong appetite increase
—
Injection site reaction
Mild erythema
—
IGF-1 elevation
Strong; monitor with chronic high-dose use
—
Cancer risk
Contraindicated in active malignancy
—
Pregnancy / OB
Avoid
Contraindicated
Nausea
—
Common, especially loading phase
Flushing
—
Common transient
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
Absolute Contraindications
GHRP-2
- ·Active malignancy
- ·Pregnancy / breastfeeding
Melanotan-II
- ·History of melanoma or atypical mole syndrome
- ·Pregnancy / breastfeeding
- ·Active uncontrolled hypertension
Relative Contraindications
GHRP-2
- ·Untreated diabetes
Melanotan-II
- ·Significant freckling / dysplastic nevus
- ·Personal or family melanoma history
05Administration Protocol
Parameter
GHRP-2
Melanotan-II
1. Reconstitution
Add 2 mL bacteriostatic water to 5 mg vial → 2.5 mg/mL.
Add 2 mL bacteriostatic water to 10 mg vial → 5 mg/mL = 500 mcg per 0.1 mL. Light-protected.
2. Injection site
SQ — abdomen or thigh. Rotate sites.
SQ — abdomen. Rotate sites.
3. Timing
Pre-sleep + fasted preferred.
Evening preferred. UV exposure (sunlight or tanning bed) helps develop tan.
4. Storage
Lyophilised: room temp, light-protected. Reconstituted: refrigerate ≤30 days.
Lyophilised: refrigerate, light-protected. Reconstituted: refrigerate ≤30 days.
5. Needle
29–31G, 4–8 mm insulin syringe.
29–31G insulin syringe.
06Stack Synergy
GHRP-2
+ CJC-1295 (no DAC)
StrongGHRP-2 + CJC-1295-no-DAC is a higher-amplitude alternative to the ipamorelin + CJC-1295 stack. GHRP-2 produces a stronger pulse but with cortisol + prolactin signal — choose when maximum GH amplitude is the goal and the side-effect tolerance is acceptable.
- GHRP-2
- 100–200 mcg SQ · pre-sleep
- CJC-1295 (no DAC)
- 100 mcg SQ · same injection
- Primary benefit
- High-amplitude GH pulse, body composition
Melanotan-II
— no documented stacks