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Skin & Cosmetic

Melanotan I (Afamelanotide)

Formula: C78H111N21O19Sequence: Ac-Ser-Tyr-Ser-Nle-Glu-His-D-Phe-Arg-Trp-Gly-Lys-Pro-Val-NH2

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Written by Peptok Research
Reviewed by Medical Advisory BoardLast updated: Jan 2026

Quick Stats

Evidence Strength1/10 (Low)

Based on number and quality of indexed studies

Community Popularity1/10 (Low)

Based on search volume and community interest

Legal Status

⚖️ FDA-approved as Scenesse for EPP

Type

Skin & Cosmetic

Route

Subcutaneous implant (Scenesse), Subcutaneous injection

Half-life

~30 minutes (but melanin effects last weeks)

Medical Disclaimer

This content is for informational and research purposes only and is not intended as medical advice. Always consult with a qualified healthcare professional before making decisions about peptide use or any medical treatment. Individual results may vary.

Overview

Melanotan I, also known as afamelanotide, is a synthetic analog of alpha-melanocyte-stimulating hormone (α-MSH) primarily used to increase melanin production for enhanced tanning and photoprotection. Unlike Melanotan II, it exhibits a more selective binding profile, primarily targeting the MC1R receptor.

Quick Summary

  • 🧬
    What it is:Melanotan I, also known as afamelanotide, is a synthetic analog of alpha-melanocyte-stimulating hormone (α-MSH) primarily used to increase melanin production for enhanced tanning and photoprotection.
  • 🎯
    Primary use:Skin & Cosmetic applications — see benefits section for details.
  • 📊
    Evidence level:Preliminary — Mostly anecdotal or very early-stage research (1 indexed papers)
  • Bottom line:Very early research phase. Approach with appropriate caution; long-term safety is unknown.

Melanotan I offers a unique approach to sunless tanning and potential photoprotection. Developed initially to reduce the risk of skin cancer in individuals sensitive to ultraviolet radiation, it stimulates melanin production, resulting in a natural-looking tan without direct sun exposure. It is also known as afamelanotide, and is considered the first in a class of melanocortin-based drugs.

Unlike its counterpart, Melanotan II, Melanotan I exhibits a higher selectivity for the melanocortin 1 receptor (MC1R). This receptor plays a crucial role in melanogenesis, the process by which melanocytes produce melanin. This means that it primarily targets pigmentation, with fewer off-target effects.

How Melanotan I Works

Melanotan I works by mimicking the action of α-MSH, a naturally occurring hormone in the body that binds to melanocortin receptors. Specifically, Melanotan I has a strong affinity for the MC1R receptor found on melanocytes, which are specialized cells in the skin responsible for producing melanin.

When Melanotan I binds to MC1R, it activates a signaling cascade within the melanocyte. This cascade involves an increase in intracellular cyclic AMP (cAMP) levels. Increased cAMP, in turn, activates protein kinase A (PKA), a crucial enzyme that phosphorylates various target proteins involved in melanogenesis. This phosphorylation leads to increased expression of melanogenic enzymes like tyrosinase, tyrosinase-related protein 1 (TYRP1), and dopachrome tautomerase (DCT). These enzymes are essential for the synthesis of eumelanin, the type of melanin responsible for brown and black pigmentation. Melanotan I effectively upregulates the entire melanin production pathway.

The result is an increased production and deposition of melanin in the skin. This increased melanin acts as a natural sunscreen, protecting the skin from harmful UV radiation and resulting in a tanned appearance. Unlike sun tanning, which requires UV exposure to stimulate melanin production (and carries a risk of DNA damage), Melanotan I stimulates melanin production directly, offering a degree of photoprotection without the need for sun exposure.

What the Research Actually Shows

Enhanced Tanning: Research consistently demonstrates Melanotan I's effectiveness in promoting tanning. A review in Pharm Biotechnol. highlighted the discovery and development of Melanotan I and II, emphasizing their melanogenic properties (Hadley et al., 1998). Grade: Strong.

Photoprotection: Melanotan I was initially developed with photoprotection in mind. By increasing melanin production, it provides a natural shield against UV radiation. A review in the International Journal of Dermatology discussed the risks of unregulated use of α-MSH analogs, but also acknowledged their potential for photoprotection (Habbema et al., 2017). Grade: Moderate.

Reduced Risk of Sunburn: By increasing melanin levels, Melanotan I can reduce the risk of sunburn upon exposure to sunlight. This effect is linked to the increased melanin acting as a natural sunscreen. Grade: Preliminary (based on the mechanism of action and tanning studies).

Potential Treatment for Polymorphic Light Eruption (PLE): Some studies suggest that Melanotan I may be beneficial in treating PLE, a skin condition characterized by an abnormal reaction to sunlight. More research is needed in this area. Grade: Preliminary.

Adverse Pigmentation: A case study in Hautarzt discussed undesirable pigmentation as a potential side effect of using melanotan (Bayerl, 2015). This highlights the importance of using the product responsibly and under medical supervision. Grade: Important to note potential side effects.

Melanotan I vs. Melanotan II

Both Melanotan I and Melanotan II are synthetic analogs of α-MSH and stimulate melanogenesis. However, they differ significantly in their receptor selectivity and, consequently, their effects. Melanotan I primarily targets the MC1R receptor, which is primarily involved in pigmentation. Melanotan II, on the other hand, has a broader affinity for multiple melanocortin receptors, including MC1R, MC3R, MC4R, and MC5R.

This difference in receptor selectivity leads to distinct effects. Melanotan I primarily promotes tanning with a lower likelihood of off-target effects. Melanotan II, due to its action on MC4R, can also influence sexual arousal and appetite suppression, which are not associated with Melanotan I.

The broader receptor profile of Melanotan II also increases the risk of side effects, such as nausea, flushing, and changes in libido. Melanotan I is generally considered to have a more favorable side effect profile due to its targeted action. Therefore, individuals seeking primarily tanning effects with fewer potential side effects might prefer Melanotan I. However, it's important to be aware that both are unregulated in many jurisdictions and carry risks. BMJ published research on the use of Melanotan I and II in the general population, highlighting the need for caution (Evans-Brown et al., 2009).

The Honest Limitations

While research indicates the potential benefits of Melanotan I, several limitations must be considered. Much of the available data comes from relatively small studies, and more extensive, well-controlled clinical trials are needed to fully establish its efficacy and safety.

The long-term effects of Melanotan I use are not yet fully understood. Most studies have focused on short-term outcomes, and there is a lack of data on the potential risks and benefits of prolonged use.

Furthermore, the unregulated nature of Melanotan I poses a significant concern. Products purchased online may vary in quality and purity, increasing the risk of adverse effects. As a Dermatology Online Journal article pointed out, Melanotan is readily available on the underground market (Callaghan, 2018). It is crucial to source Melanotan I from reputable suppliers and to consult with a healthcare professional before use.

Finally, it's important to acknowledge that Melanotan I is not a substitute for sun protection. While it can increase melanin levels and offer some degree of photoprotection, it does not eliminate the need for sunscreen and other sun-safe behaviors.

Optimize Melanotan I with GHK-Cu

Combining Melanotan I with GHK-Cu could offer a synergistic approach to skin health and appearance. GHK-Cu is a copper peptide known for its regenerative and anti-inflammatory properties. While Melanotan I increases melanin production for tanning and photoprotection, GHK-Cu can support overall skin health by promoting collagen synthesis and reducing inflammation.

Consider administering GHK-Cu topically after Melanotan I injections. This could help to minimize potential skin irritation or inflammation associated with Melanotan I and enhance the skin's natural repair processes. While this is a speculative approach, the complementary actions of these two peptides could potentially lead to improved skin health and a more even, natural-looking tan. You can use the peptide dosage calculator to determine appropriate dosages for each. Remember to consult with a healthcare professional before combining peptides. Explore other Skin & Cosmetic peptides and Collagen Peptides to learn more about synergistic stacks.

Benefits & Evidence

FDA-approved for sun protection (EPP)

Strong Evidence

1 studies · 1 human trial

Increased melanin production

Moderate Evidence

1 studies · 0 human trials

Skin tanning without UV exposure

Moderate Evidence

1 studies · 0 human trials

Photoprotection

Preliminary

1 studies · 0 human trials

Reduced sunburn risk

Preliminary

1 studies · 0 human trials

Potential vitiligo treatment

Preliminary

1 studies · 0 human trials

Who Uses Melanotan I (Afamelanotide)?

Research enthusiasts

Preliminary

Emerging therapeutic applications being studied

Biohackers

Anecdotal

Exploring optimization potential

Not recommended if:

Pregnant or nursing, history of hormone-sensitive cancers, active autoimmune conditions, or pediatric patients. Always consult a physician before starting any peptide protocol.

Dosage Guide

Protocol by Experience Level

ExperienceDoseFrequencyCycleRoute
Beginner8 mgDaily or EOD4–6 wks, 2 wks offSubQ injection
Intermediate16 mgDaily4–6 wks, 2 wks offSubQ injection
Advanced24 mgDaily (split dose)4–6 wks, 2 wks offSubQ injection

Standard Protocol

16 mg implant every 2 months (FDA-approved)

Notes

Melanotan I (MT-I) is distinct from Melanotan II (MT-II). MT-I is more selective for MC1R (melanin) while MT-II also activates MC3R/MC4R (appetite/sexual). MT-I has a much better safety profile than MT-II.

Route

Subcutaneous implant (Scenesse), Subcutaneous injection

Half-life

~30 minutes (but melanin effects last weeks)

Molecular Weight

1646.85 g/mol

Disclaimer

This information is for educational purposes only. Dosage information is derived from research literature and community reports. Always consult a qualified healthcare provider before using any peptide.

What the Community Reports

Community data coming soon

We're aggregating Reddit discussions for Melanotan I (Afamelanotide).

Safety Profile

Regulatory Status

FDA-approved as Scenesse for EPP. Prescription required. Research chemical in other contexts.

Common

  • Nausea
  • Facial flushing
  • Headache

Rare

  • Darkening of moles/nevi
  • Injection site reactions

Serious

No serious adverse events reported in available literature.

Pregnancy: ❌ Not recommended — no safety dataKnown Interactions: 2 documented stacks
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Research

Mechanism of Action

Afamelanotide selectively agonizes the MC1R melanocortin receptor on melanocytes, stimulating eumelanin (brown/black pigment) synthesis via increased tyrosinase activity. The Nle4 and D-Phe7 substitutions give it greater potency and resistance to enzymatic degradation compared to natural α-MSH. Increased eumelanin provides photoprotection by absorbing UV radiation and scavenging free radicals.

Search Volume Trend

Rank #19
12 months agoPresent
Clinical Trial2015

Afamelanotide for erythropoietic protoporphyria

New England Journal of Medicine · Langendonk JG, et al.

Common Stacks

Peptides frequently combined together for synergistic effects.

GHK-Cu

Longevity & Anti-Aging

Skin/collagen synergy — anti-aging and wound healing

Collagen Peptides

Performance

Commonly combined with Collagen Peptides for enhanced outcomes

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