Menu
Peptide Database
Results
No peptides found
Featured

Use search to browse all 100+ peptides

Melanotan-I

Afamelanotide, MT-I, [Nle4-D-Phe7]-α-MSH, Scenesse, CUV-1647

Quick Stats
Studies 225
Trials 100
Score 1
2024 pubmed 1 citations

Recommended Tool Compounds for the Melanocortin Receptor (MCR) G Protein-Coupled Receptors (GPCRs).

Weirath. Nicholas A NA; Haskell-Luevano. Carrie C

Key Findings

  • Melanocortin receptors have five subtypes that affect pigmentation, steroid production, and metabolism.
  • Synthetic derivatives of the natural hormone α‑MSH (e.g., NDP‑MSH, melanotan I, melanotan II) are now established as powerful research ligands.
  • These tool compounds are used to validate cell lines, support cryo‑EM studies of active/inactive receptor states, and serve as scaffolds for developing FDA‑approved drugs.

Practical Outcomes

  • For the biohacker community, the paper mainly provides background on why these peptides are valuable in the lab and may become future therapeutics. It does not offer dosing guidelines, safety data, or actionable protocols for personal use, so its immediate practical relevance is low.

Summary

This review talks about a handful of synthetic peptides (like melanotan I, melanotan II, and SHU9119) that scientists use as research tools to study melanocortin receptors, which are involved in skin color, hormone production, and energy balance. It explains how these compounds help map receptor structures and guide drug discovery, but it doesn't give any practical advice on how to use them in humans.

Abstract

The melanocortin receptors are a centrally and peripherally expressed family of Class A GPCRs with physiological roles, including pigmentation, steroidogenesis, energy homeostasis, and others yet to be fully characterized. There are five melanocortin receptor subtypes that, apart from the melanocortin-2 receptor (MC2R), are stimulated by a shared set of endogenous agonists. Until 2020, X-ray crystallographic and cryo-electron microscopic (cryo-EM) structures of these receptors were unavailable, and the investigation of their mechanisms of action and putative ligand-receptor interactions was driven by site-directed mutagenesis studies of the receptors and targeted structure-activity relationship (SAR) studies of the endogenous and derivative synthetic ligands. Synthetic derivatives of the endogenous agonist ligand α-MSH have evolved into a suite of powerful ligands such as NDP-MSH (melanotan I), melanotan II (MTII), and SHU9119. This suite of tool compounds now enables the study of the melanocortin receptors and serves as scaffolds for FDA-approved drugs, means of validating stably expressing melanocortin receptor cell lines, core ligands in assessing cryo-EM structures of active and inactive receptor complexes, and essential references for high-throughput discovery and mechanism of action studies. Herein, we review the history and significance of a finite set of these essential tool compounds and discuss how they are being utilized to further the field's understanding of melanocortin receptor physiology and greater druggability.

Study Information

Provider

pubmed

Year

2024

Date

2024-08-26T00:00:00.000Z

DOI

10.1021/acsptsci.4c00129

Citations

1

References

135