β-Melanocyte Stimulating Hormone (MSH), human

β-Melanocyte Stimulating Hormone (MSH), human, a 22-residue peptide, acts as an endogenous melanocortin-4 receptor (MC4-R) agonist.

Designed for biological research and industrial applications, not intended for individual clinical or medical purposes.
β-Melanocyte Stimulating Hormone (MSH), human(CAS 17908-57-5)

CAT No: R1797

CAS No:17908-57-5

Synonyms/Alias:BETA-MSH, HUMAN;Beta-MSH (1-22) (human);17908-57-5;beta-MSH (human) trifluoroacetate salt;DA-59364;Q20707037;

Custom Peptide Synthesis
cGMP Peptide
  • Registration of APIs
  • CMC information required for an IND
  • IND and NDA support
  • Drug master files (DMF) filing
M.F/Formula
C118H174N34O35S
M.W/Mr.
2660.9
Sequence
One Letter Code:AEKKDEGPYRMEHFRWGSPPKD
Three Letter Code:H-DL-Ala-DL-Glu-DL-Lys-DL-Lys-DL-Asp-DL-Glu-Gly-DL-Pro-DL-Tyr-DL-Arg-DL-Met-DL-Glu-DL-His-DL-Phe-DL-Arg-DL-Trp-Gly-DL-Ser-DL-Pro-DL-Pro-DL-Lys-DL-Asp-OH
Purity
≥95% (HPLC)

β-Melanocyte Stimulating Hormone (MSH), human is a naturally occurring peptide hormone belonging to the melanocortin family, with a primary structure derived from the pro-opiomelanocortin (POMC) precursor. As a bioactive peptide, it plays a significant role in the regulation of melanogenesis, influencing pigmentation processes in human physiology. Its interaction with melanocortin receptors, particularly MC1R, underpins its functional significance in both fundamental and applied biochemical research. The availability of synthetic human β-MSH enables controlled investigations into peptide-receptor dynamics, signal transduction pathways, and the broader physiological effects of melanocortins.

Receptor binding studies: β-MSH is widely utilized in receptor pharmacology research to characterize the binding affinities, selectivity, and activation profiles of melanocortin receptors. By serving as a reference ligand for MC1R and related receptors, it enables the elucidation of ligand-receptor interactions, competitive binding mechanisms, and downstream signaling events. These studies are essential for mapping receptor functionality and understanding the molecular basis of peptide-mediated signaling.

Signal transduction analysis: Researchers employ β-MSH to probe intracellular signaling cascades initiated by melanocortin receptor activation. Through its engagement with G protein-coupled receptors, the peptide triggers cAMP-dependent pathways and modulates secondary messenger systems. Investigations using β-MSH facilitate the dissection of these biochemical pathways, supporting the identification of key regulatory nodes and contributing to the broader understanding of peptide hormone signaling in cellular contexts.

Pigmentation research: The peptide is a critical tool in studies of melanogenesis and pigmentation biology. By stimulating melanin synthesis in cultured melanocytes, β-MSH provides a model for examining the regulation of pigment production, enzyme activity, and gene expression associated with skin and hair coloration. Such applications are instrumental in advancing knowledge of pigmentary disorders, cellular differentiation, and the genetic determinants of pigmentation.

Peptide structure-activity relationship (SAR) studies: β-MSH serves as a reference molecule in peptide engineering and SAR investigations. By systematically modifying its amino acid sequence or chemical structure, researchers can assess how specific residues contribute to receptor affinity, biological potency, and metabolic stability. These studies inform the rational design of novel peptide analogs with tailored pharmacological properties, supporting drug discovery and the development of research tools.

Analytical method development: The peptide is frequently used as a standard or control in the validation of analytical techniques such as high-performance liquid chromatography (HPLC), mass spectrometry, and immunoassays. Its defined sequence and bioactivity make it suitable for calibrating assay sensitivity, optimizing detection parameters, and ensuring reproducibility in peptide quantification workflows. These applications underpin quality control and methodological rigor in peptide research laboratories.

Long-term Storage Conditions
10 mM in H2O
Shipping Condition
Room temperature in continental US; may vary elsewhere.
InChI
InChI=1S/C118H174N34O35S/c1-63(122)97(167)135-77(36-39-93(159)160)105(175)137-71(23-8-11-42-119)100(170)136-72(24-9-12-43-120)102(172)147-84(55-95(163)164)111(181)140-76(35-38-92(157)158)98(168)132-60-91(156)150-47-16-28-87(150)112(182)148-81(52-65-31-33-68(154)34-32-65)109(179)138-74(26-14-45-128-117(123)124)101(171)142-79(41-50-188-2)107(177)141-78(37-40-94(161)162)106(176)146-83(54-67-58-127-62-133-67)110(180)144-80(51-64-19-4-3-5-20-64)108(178)139-75(27-15-46-129-118(125)126)103(173)145-82(53-66-57-130-70-22-7-6-21-69(66)70)99(169)131-59-90(155)134-86(61-153)114(184)152-49-18-30-89(152)115(185)151-48-17-29-88(151)113(183)143-73(25-10-13-44-121)104(174)149-85(116(186)187)56-96(165)166/h3-7,19-22,31-34,57-58,62-63,71-89,130,153-154H,8-18,23-30,35-56,59-61,119-122H2,1-2H3,(H,127,133)(H,131,169)(H,132,168)(H,134,155)(H,135,167)(H,136,170)(H,137,175)(H,138,179)(H,139,178)(H,140,181)(H,141,177)(H,142,171)(H,143,183)(H,144,180)(H,145,173)(H,146,176)(H,147,172)(H,148,182)(H,149,174)(H,157,158)(H,159,160)(H,161,162)(H,163,164)(H,165,166)(H,186,187)(H4,123,124,128)(H4,125,126,129)
InChI Key
XLLJFSCSXTYVTN-UHFFFAOYSA-N

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