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Neuropeptide

Alpha-MSH

Alpha-MSH (alpha-melanocyte-stimulating hormone) is a 13-amino-acid melanocortin peptide processed from POMC. Research examines its roles in pigmentation, appetite regulation, and inflammation signaling.

By The Peptides Codex Editorial TeamIndividual review date not recorded

Page data last changed: . Registry refreshes and identity assessments are separate from scientific content review.

Reference backbone length
13 positions
Class
Neuropeptide
Function
Melanocortin signaling: pigmentation and appetite
Context
Pigmentation and energy-balance research

POMC-derived melanocortin corresponding to the ACTH(1–13) sequence.

Also known as: α-MSH · Alpha-melanocyte-stimulating hormone

Part of the Neuropeptides & signaling cluster

Overview

Alpha-MSH (alpha-melanocyte-stimulating hormone) is a 13-amino-acid melanocortin peptide processed from POMC. Research examines its roles in pigmentation, appetite regulation, and inflammation signaling.

Source & context

Biological / chemical source: Pituitary and hypothalamus; derived from POMC

Primary research or clinical context: Pigmentation and energy-balance research

Melanocortin receptors

Alpha-MSH activates melanocortin receptors (MC1R–MC5R), linking a single peptide to pigmentation, energy balance, and immune signaling depending on receptor and tissue. This receptor breadth drives broad research interest.

Relationship to related peptides

Its sequence is identical to the first 13 residues of ACTH, and it is the natural counterpart to synthetic melanocortin research peptides. This page covers that biology for education, not cosmetic or therapeutic use.

Sequence of the selected reference form

Sequence backbone for the reference form: Human alpha-MSH, N-acetyl-Ser1 and C-terminal Val13 amide. Termini, stereochemistry and modifications are described below.

SYSMEHFRWGKPV

SYSMEHFRWGKPV

Analyze sequences in the playground →

Structure & chemistry

Molecular identity & reference confidence

Source-supported reference

Select the mono-N-acetylated, C-terminally amidated 13-residue alpha-MSH form. Original normal-human-pituitary work documents non- and mono-acetylated alpha-MSH; this decision explicitly chooses the acetylated parent rather than treating all forms as one. Reviewed POMC provides the human backbone; its N-acetyl/amide annotations include by-similarity evidence, independently corroborated here by original human chemistry and the PubChem graph.

Molecular form
Human alpha-MSH, N-acetyl-Ser1 and C-terminal Val13 amide
Species
Homo sapiens
Termini (N / C)
N-acetylated L-serine alpha-amino group / L-valine carboxamide (-CONH2)

Average reference mass · Molecular identity assessment: 2026-10-05

Reference policy updated: 2026-10-05

Full sequence with modifications

Ac-Ser-Tyr-Ser-Met-Glu-His-Phe-Arg-Trp-Gly-Lys-Pro-Val-NH2

Molecular formula
C77H109N21O19S
Average reference mass
≈ 1,664.9
Backbone
Human alpha-MSH, N-acetyl-Ser1 and C-terminal Val13 amide
C-terminus
L-valine carboxamide (-CONH2)
Identifiers

Chemistry values: curated profile, PubChem.

Clinical development snapshot

ClinicalTrials.gov lists 10 registered studies with “Alpha-MSH” as an intervention (snapshot 2026-09-06). A registry footprint is not evidence of efficacy or approval.

Registered studies
10
Highest phase reached
Phase 3
Active in latest 100
1
Most recent update
2026-02-06
Most recently updated studies
NCTTitlePhaseStatusUpdated
NCT03510533Validation of the Concept of the Autoantibodies Directed Against the Neuropeptides Involved in Food Intake RegNot applicablecompleted2026-02-06
NCT06825182Current Status of Islet Alpha Cell Function in Patients with Type 2 DiabetesPhase 3recruiting2025-02-13
NCT05709444A Phase IIb, Multicenter, Open-Label, Prospective Study of Bremelanotide in Diabetic Kidney DiseasePhase 2completed2024-10-17
NCT06293664Protocol for Alpha MSH Infusion Study in Patients With Type 2 DiabetesNot applicableunknown2024-03-05
NCT03451578Alpha MSH in Ocular DiseaseNot applicablecompleted2022-12-22
NCT023330711. Study to Evaluate the Efficacy/Safety of Bremelanotide in Premenopausal Women With Hypoactive Sexual DesirePhase 3completed2021-04-09
See all on ClinicalTrials.gov →
Concentration math

Alpha-MSH — reconstitution calculator

Enter how much peptide is in the vial and how much diluent (e.g. bacteriostatic water) is added. The tool returns the resulting solution concentration — and, for any amount you type, the volume it corresponds to. This is educational arithmetic, not a dosing recommendation.

Reference form: Human alpha-MSH, N-acetyl-Ser1 and C-terminal Val13 amideAverage reference mass: 1,664.9 Da

Syringe graduation
Solution concentration
5 mg/mL5,000 mcg/mL
mcg

Enter an amount to see the volume it corresponds to.

Educational concentration mathematics only. This tool does not recommend a dose, amount, or protocol, and nothing here is medical advice. Many peptides are not authorized by Health Canada for human use — see our reconstitution and bacteriostatic-water guides for context.

Open the Alpha-MSH calculator on its own page →

FAQ about Alpha-MSH

What is Alpha-MSH?+

Alpha-MSH (alpha-melanocyte-stimulating hormone) is a 13-amino-acid melanocortin peptide processed from POMC. Research examines its roles in pigmentation, appetite regulation, and inflammation signaling.

What Canadian product status is recorded for Alpha-MSH?+

Canadian product status for Alpha-MSH has not been verified in this profile. No verified record here does not mean no authorization exists. Status depends on the product, formulation and use; consult Health Canada's product records.

What is the length of the selected reference form for Alpha-MSH?+

The selected reference form (Human alpha-MSH, N-acetyl-Ser1 and C-terminal Val13 amide) has 13 residues or residue-derived units in its backbone. Other forms in this family may have a different length.

Related peptides

References & further reading

  1. 1.Xu et al. (2022). Pituitary hormone α-MSH promotes tumor-induced myelopoiesis and immunosuppression. Science
  2. 2.Luger et al. (2015). An α-MSH analog in erythropoietic protoporphyria. J Invest Dermatol
  3. 3.Dall'Olmo et al. (2023). Alpha-melanocyte stimulating hormone (α-MSH): biology, clinical relevance and implication in melanoma. J Transl Med
  4. 4.Wang et al. (2019). α-melanocyte stimulating hormone (α-MSH) promotes osteoblast differentiation of MC3T3-E1 cells. Eur J Pharmacol
  5. 5.Watanabe et al. (2024). Intraperitoneal administration of α-melanocyte stimulating hormone (α-MSH) suppresses food intake and induces anxiety-like behavior via the brain MC4 receptor-signaling pathway in goldfish. J Neuroendocrinol
  6. 6.Fenselau et al. (2017). A rapidly acting glutamatergic ARC→PVH satiety circuit postsynaptically regulated by α-MSH. Nat Neurosci
  7. 7.Ichiyama et al. (2000). The neuroimmunomodulatory peptide alpha-MSH. Ann N Y Acad Sci
  8. 8.Watanabe et al. (2021). Intracerebroventricular administration of α-melanocyte-stimulating hormone (α-MSH) enhances thigmotaxis and induces anxiety-like behavior in the goldfish Carassius auratus. Peptides
  9. 9.PubChem — compound summary for alpha-MSH (CID 16133793)
  10. 10.Wikipedia — Melanocyte-stimulating hormone
Disclaimer: Educational content only. Not medical advice. Not instructions for human use. Research peptides and unapproved products may be restricted or illegal to market for human consumption in your jurisdiction. Consult qualified professionals and applicable law.
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