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

AdamaxvsMelanotan-II

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

AAnimal-StrongHUMAN-REVIEWED20/47 cited
BPhase 1HUMAN-REVIEWED9/43 cited
Adamax
ACTH(4-10) Analogue · Russian Nootropic
1.4×BDNF protein ↑Dolotov 2006
BDNF mRNA (exon III)Dolotov 2006
1.6×trkB phosphorylationDolotov 2006
Intranasal · Research Use Only
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
Adamax
Melanotan-II
Primary target
Melanocortin receptors (MC-Rs) in hippocampus and cortex
MC1R (skin) + MC3R + MC4R (CNS sexual / appetite)Dorr 1996
Pathway
ACTH(4-10) fragment → MC-R binding → BDNF/trkB upregulation → neurotrophic signaling
MC1R agonism → melanocyte tyrosinase → eumelanin synthesis. MC4R → autonomic sexual arousal centresDorr 1996Simerly 2023
Downstream effect
Increased hippocampal BDNF expression, trkB tyrosine phosphorylation, enhanced conditioned avoidance learning, circadian rhythm normalizationDolotov 2006Arushanian 2008
Skin darkening, photo-protection, increased sexual desire / spontaneous erectionDorr 1996
Feedback intact?
Non-endocrine — devoid of adrenal axis effectsvan 1978
Origin
ACTH(4-10) fragment with modified amino acid sequence at positions 8, 9, 10Teter 2001
Cyclic 7-AA modified α-MSH analog; designed at University of ArizonaDorr 1996
Antibody development

02Dosage Protocols

Parameter
Adamax
Melanotan-II
Animal dose (rat)
50 mcg/kg body weightDolotov 2006
Single intranasal application; produced maximal BDNF response.
Route
Frequency
Single-dose or chronic administration protocols
Chronic dosing normalized circadian rhythms; single-dose produced acute BDNF elevation.
Daily during loading; 1–2× per week maintenance
Human dose (exploratory)
Not established — limited human data
ACTH(4-10) and analogs dosed 30–60 mcg intranasally in early human studies.
Evidence basis
Animal (rodent, rabbit) studies; minimal human RCT data
Phase 1 + anecdotalDorr 1996
Timing
Variable — chronic administration for circadian effects
Evening preferred (24h tan-development cycle)
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.
Duration
8–12 weeks per cycle
Reconstitution
Bacteriostatic water; protect from light
Half-life
~1 hour plasma; effects on melanocytes persist days

04Side Effects & Safety

Parameter
Adamax
Melanotan-II
Cardiovascular effects
ACTH(4-10) fragments may have pressor and cardioaccelerator actions at high dosesGruber 1984
Effects attenuated by α/β-receptor antagonists; observed at 30–1000 nmol/kg IV in rats.
Natriuretic effect
ACTH(4-10) exhibited natriuretic activity at lower doses (7 nmol/kg)Gruber 1984
Behavioral suppression
Suppression of aggression, reduced orientation-cognition reactions in rabbitsTeter 2001
May reflect anxiolytic or stress-dampening profile.
Long-term safety
Unknown — chronic human safety data lacking
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
Adamax
  • ·Pregnancy and lactation (precautionary; no data)
  • ·Active cardiovascular instability (due to potential pressor effects)
Melanotan-II
  • ·History of melanoma or atypical mole syndrome
  • ·Pregnancy / breastfeeding
  • ·Active uncontrolled hypertension
Relative Contraindications
Adamax
  • ·Hypertension (monitor BP if using higher doses)
  • ·Renal impairment (natriuretic effects may alter electrolyte balance)
Melanotan-II
  • ·Significant freckling / dysplastic nevus
  • ·Personal or family melanoma history

05Administration Protocol

Parameter
Adamax
Melanotan-II
1. Reconstitution (if lyophilised)
Add sterile water or bacteriostatic water to lyophilised vial per manufacturer guidance. Roll gently — do not shake. Ensure clarity before use.
Add 2 mL bacteriostatic water to 10 mg vial → 5 mg/mL = 500 mcg per 0.1 mL. Light-protected.
2. Route
Intranasal administration is the primary route in animal and exploratory human studies. Delivered via nasal spray or dropper to ensure mucosal absorption.Dolotov 2006Smolnik 2000
SQ — abdomen. Rotate sites.
3. Timing
Variable. Single-dose protocols for acute cognitive tasks; chronic daily dosing for circadian rhythm normalization and sustained neuroprotection.
Evening preferred. UV exposure (sunlight or tanning bed) helps develop tan.
4. Storage
Lyophilised: room temperature, light-protected. Reconstituted: refrigerate 2–8 °C, use within manufacturer-specified timeframe.
Lyophilised: refrigerate, light-protected. Reconstituted: refrigerate ≤30 days.
5. Needle
29–31G insulin syringe.

06Stack Synergy

Adamax
+ Semax
Moderate
View Semax

Both Adamax and Semax are ACTH(4-10)-derived nootropics acting via melanocortin receptors and BDNF upregulation. Adamax has distinct amino acid modifications at positions 8-10, potentially offering complementary receptor binding profiles or metabolic stability. Stacking may amplify neurotrophic signaling and cognitive enhancement, though direct synergy studies are absent. Theoretical multi-pathway benefit.

Adamax
Research dose intranasal
Semax
300–600 mcg intranasal
Frequency
Once daily, morning or pre-cognitive task
Primary benefit
Enhanced BDNF upregulation, cognitive performance, neuroprotection
Melanotan-II
— no documented stacks