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α-MSH

Cat. No. M9572

All AbMole products are for research use only, cannot be used for human consumption.

α-MSH Structure
Synonym:

α-Melanocyte stimulating hormone; α-Melanotropin

Size Price Availability Quantity
1mg USD 65  USD65 In stock
5mg USD 185  USD185 In stock
10mg USD 320  USD320 In stock
25mg USD 640  USD640 In stock
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Biological Activity

α-MSH (α-Melanocyte-stimulating hormone) is an anti-inflammatory agent stimulates melanocortin 1 receptor that results in the activation of adenylyl cyclase. α-Melanocyte-stimulating hormone (α-MSH) acts as an anti-inflammatory agent via down regulating the production and activity of the pro-inflammatory cytokines interleukin-1 (IL-1), tumor necrosis factor (TNF)-α and IL-6 expressed in various cells of the immune system. It also controls the nitric oxide production associated with inflammation. α-MSH inhibits nuclear factor-κB (NF-κB)-dependent gene transcription and NF-κB pathway induced by TNF and other inflammatory agents. This activity of α-MSH is mediated through the production of cyclic adenosine monophosphate (cAMP) and activation of protein kinase A (PKA) enzyme. α-MSH has an essential role to play in melanin production in animals. α-MSH regulates development of several skin diseases, including cutaneous inflammation and hyper-proliferative skin diseases.

Chemical Information
Molecular Weight 1664.88
Formula C77H109N21O19S
CAS Number 581-05-5
Solubility (25°C) Water ≥ 15 mg/mL
Storage -20°C, dry, protect from light, sealed
References

[1] Minhyeok Song, et al. Mar Drugs. Jeju Magma-Seawater Inhibits α-MSH-Induced Melanogenesis via CaMKKβ-AMPK Signaling Pathways in B16F10 Melanoma Cells

[2] Seung-Ho Seo, et al. Molecules. Metabolomics Reveals the Alteration of Metabolic Pathway by Alpha-Melanocyte-Stimulating Hormone in B16F10 Melanoma Cells

[3] Hye Yeon Lim, et al. Int J Mol Sci. Antiwrinkle and Antimelanogenesis Effects of Tyndallized Lactobacillus acidophilus KCCM12625P

[4] Wisurumuni Arachchilage, et al. Biomolecules. Anthocyanins from Hibiscus syriacus L. Inhibit Melanogenesis by Activating the ERK Signaling Pathway

[5] Ga-Young Seo, et al. Int J Mol Sci. Leathesia difformis Extract Inhibits α-MSH-Induced Melanogenesis in B16F10 Cells via Down-Regulation of CREB Signaling Pathway

[6] Hyeju Jo, et al. Bioorg Med Chem Lett. Synthesis and Biological Evaluation of Caffeic Acid Derivatives as Potent Inhibitors of α-MSH-stimulated Melanogenesis

[7] Taek-In Oh, et al. Int J Mol Sci. Plumbagin Suppresses α-MSH-Induced Melanogenesis in B16F10 Mouse Melanoma Cells by Inhibiting Tyrosinase Activity

[8] Xin-Yun Lu, et al. J Neurosci. Interaction Between Alpha-Melanocyte-Stimulating Hormone and Corticotropin-Releasing Hormone in the Regulation of Feeding and Hypothalamo-Pituitary-Adrenal Responses

Related Melanocortin Receptor Products
CRN04894 

CRN04894 is an orally active MC2R antagonist that demonstrates in vivo efficacy in rat model of adrenocorticotropic hormone (ACTH)-stimulated corticosterone secretion.

BMS-470539 

BMS-470539 is a synthetic MC-1R agonist with potent anti-inflammatory properties.

PF-00446687 

PF-00446687 is a potent, selective melanocortin-4 receptor (MC4R) agonist with EC50 of 12 ± 1 nM.

BMS-470539 dihydrochloride 

BMS-470539 dihydrochloride is a highly potent and selective melanocortin-1 receptor (MC-1R) agonist with an IC50 of 120 nM, an EC50 of 28 nM.

Undecylenoyl phenylalanine 

Undecylenoyl phenylalanine is an antagonist for α-melanocyte-stimulating hormone (MSH) and β-adrenergic receptor (β-ADR) to reduce the melanogenesis in melanocytes.

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Keywords: α-MSH, α-Melanocyte stimulating hormone; α-Melanotropin supplier, Melanocortin Receptor, inhibitors, activators

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