Melanotan I (Afamelanotide)
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Melanotan I (Afamelanotide)

Selective MC1R agonist (Scenesse) approved in EU/US for erythropoietic protoporphyria. Produces sustained melanin-based photoprotection without the behavioural

SkinLibido
● In Stock

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1+ vials
−5%
3+ vials
−10%
5+ vials
−20%
10+ vials

Total Price

$60

For research & laboratory use only. Not for human consumption.

Half-Life

~2.5 hours (linear); implant formulation provides 60-day release

Administration Route

Subcutaneous injection or implant

Controlled Tanning

Linear alpha-MSH analogue with 10x potency vs natural hormone

UV Protection

Darkens melanin before UV exposure — photoprotective mechanism

Longer Half-Life

Cyclic structure gives 24-hour activity for gradual tan

Effect Profile

Skin Tone

0%

Collagen Density

0%

Anti-Wrinkle

0%

Wound Healing

0%

Mechanism of Action

Melanotan I (afamelanotide) is a linear alpha-MSH analogue with a Nle4, D-Phe7 substitution that increases MC1R binding affinity and resistance to enzymatic degradation. It selectively activates MC1R on melanocytes, driving cAMP-mediated eumelanin (brown/black pigment) synthesis and melanosome maturation, without significant MC3R/MC4R activation. This selective MC1R profile avoids the sexual and appetite effects seen with Melanotan II.

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