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database / melanocortin

Afamelanotide

also known as Melanotan I, NDP-α-MSH, Scenesse

approved melanocortin integumentary sequence not characterised
OOOOOOOOOOOOOOOOOOONNNNNNNNNNNNNNNNNNNNNHHHHHHHHHHHHHHHHHHHHHHHHHH
118 heavy atoms · 234 bonds · drag to pan, scroll to zoom C78N21O19

Skeletal structure drawn from the computed atomic coordinates in PubChem CID 16197727. Carbons are implicit vertices; hydrogens on carbon are suppressed, as in any structural formula. Nothing here is estimated — every atom sits where PubChem placed it.

Research reference only. The observations below are recorded in the cited literature. Nothing here is advice or a recommendation, and no dosing information is published on this site.

Sequence

Primary structure not characterised in the public records this index draws on. Nothing is shown rather than something invented.

Ac-Ser-Tyr-Ser-Nle-Glu-His-D-Phe-Arg-Trp-Gly-Lys-Pro-Val-NH2 — norleucine and D-Phe substitutions on the α-MSH backbone.

Molecular data

Chemical fields come from the PubChem compound record; computed values are derived from the sequence shown above.
molecular formulaC78H111N21O19
molecular weight1646.8 Da (PubChem)
computed backbone massnot characterised
lengthnot characterised
net charge (pH 7.4)not characterised
mean hydropathynot characterised
half-lifenot characterised
delivery routesubcutaneous implant
PubChem CID16197727
PDBnot characterised
UniProt parentP01189

Mechanism

MC1R agonist; approved for erythropoietic protoporphyria.

Reported targets: MC1R

Experimental structure

No experimental structure of this peptide is deposited in the PDB. Nothing is rendered here — a predicted fold would not be a structure, and this site does not draw one.

Parent protein

Analogue of α-MSH, a POMC cleavage product. UniProt P01189 · 267 aa

Reported effects

Each row is an outcome described in the literature indexed for this peptide. Reported in the cited work — not a claim, not a recommendation.

Reported observations and the corpus they are drawn from.
reported outcomewhere it appears
melanogenesis[Hormones and skin pigmentation: fundamentals and clinical relevance] Dermatologie (Heidelberg, Germany) 2026
phototoxicity reduction in trialsGerman Cohort Observational Study to Investigate the Short- and Long-Term Sa… Photodermatology, photoimmunology & photomedicine 2025

Registered trials

Records from ClinicalTrials.gov. Listed for reference — this project sponsors no trial and is not involved in any of them.
NCTtitlestatusphase
NCT00979745Phase III Confirmatory Study in Erythropoietic Protoporphyria (EPP)COMPLETEDPHASE3
NCT05159752A Study to Evaluate the Safety and Efficacy of Afamelanotide in Patients With Xeroderma PigmUNKNOWNPHASE2
NCT04053270Multicentre Phase III Erythropoietic Protoporphyria StudyCOMPLETEDPHASE3
NCT04578496A Safety Extension Study in Patients With Erythropoietic Protoporphyria (EPP)COMPLETEDPHASE3
NCT06388642Pharmacokinetics of Afamelanotide in Erythropoietic Protoporphyria PatientsCOMPLETEDPHASE1, PHASE2

Literature (8)

[Hormones and skin pigmentation: fundamentals and clinical relevance] — Dermatologie (Heidelberg, Germany) 2026

abstract not reproduced — this record is not open-access, so it is linked rather than copied.

publisher record ↗ · PMID 41489668 · DOI 10.1007/s00105-025-05636-4

German Cohort Observational Study to Investigate the Short- and Long-Term Safety and Clinical Effectiveness of Afamelanotide 16 mg (SCENESSE) in Patients With Erythropoietic Protoporphyria (EPP) — Photodermatology, photoimmunology & photomedicine 2025

BackgroundAfamelanotide 16 mg (SCENESSE) is the first approved treatment for erythropoietic protoporphyria (EPP). EPP is a rare autosomal recessive inherited disorder of the haem biosynthesis pathway, where patients experience severe and debilitating acute phototoxicity. It affects at least one in 140,000 of the European population. A postauthorisation safety study (PASS) and a disease registry were imposed as conditions of the European marketing authorisation.ObjectivesEvaluate the short- and long-term safety and clinical effectiveness of afamelanotide 16 mg in EPP patients enrolled in the PASS in Germany.MethodsThe PASS (EUPAS13004) is an ongoing observational study collecting safety and effectiveness variables from treated and untreated EPP patients in the European EPP Disease Registry. Patients (n = 200, none untreated) received afamelanotide according to the summary of product chara…

open access ↗ · PMID 40082741 · DOI 10.1111/phpp.13012

The α-MSH-MC1R Axis Modulates Sex-Specific Senescence and Inflammation Processes in Human Articular Chondrocytes and Mice Knee Joints — Aging and disease 2026

abstract not reproduced — this record is not open-access, so it is linked rather than copied.

publisher record ↗ · PMID 41824482 · DOI 10.14336/ad.2025.1307

Afamelanotide improves quality of life and light tolerance in Austrian erythropoietic protoporphyria patients — Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG 2026

abstract not reproduced — this record is not open-access, so it is linked rather than copied.

publisher record ↗ · PMID 41793078 · DOI 10.1111/ddg.15996

Adjunctive use of Polypodium leucotomos extract in patients with erythropoietic protoporphyria: An exploratory study — Photochemistry and photobiology 2026

abstract not reproduced — this record is not open-access, so it is linked rather than copied.

publisher record ↗ · PMID 41766687 · DOI 10.1111/php.70081

New and currently investigated pharmacotherapies for the erythropoietic protoporphyrias: spotlight on dersimelagon and bitopertin — Expert opinion on pharmacotherapy 2026

abstract not reproduced — this record is not open-access, so it is linked rather than copied.

publisher record ↗ · PMID 41885813 · DOI 10.1080/14656566.2026.2651281

New pharmacotherapies for the erythropoietic protoporphyrias: an analysis of trial protocols from a patient perspective — Orphanet journal of rare diseases 2025

BACKGROUND: The erythropoietic protoporphyrias (EPP) are a group of ultra-rare (1:100.000) inborn errors of the heme biosynthesis characterised by painful phototoxic reactions in tissue exposed to visible light. Afamelanotide is the only approved treatment for EPP and effectively prevents phototoxic reactions and improves the quality of life of the patients. In the past years, several new potential treatment options for EPP have been identified, some of which are currently under investigation in clinical trials. While these developments could improve patient care, it is important to know how safety and efficacy of drug candidates compare to the existing treatment, i.e. afamelanotide. METHODS: We identified pharmacotherapies (leaving out, for example, topical applications such as sunscreens or supplements such as iron) which are currently (that is, within the last 5 years) evaluated for E…

open access ↗ · PMID 41466311 · DOI 10.1186/s13023-025-04170-9

From darkness to light: Case report on afamelanotide-treatment in a 9-year-old child with erythropoietic protoporphyria — JAAD case reports 2026

abstract not reproduced — this record is not open-access, so it is linked rather than copied.

open access ↗ · PMID 41542313 · DOI 10.1016/j.jdcr.2025.11.022

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