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
Intranasal · Research Use Only
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
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.
—
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.
—
Timing
Variable — chronic administration for circadian effects
Evening preferred (24h tan-development cycle)
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.
—
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
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
ModerateBoth 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