Eloralintide

Eloralintide

Nazwa produktu Eloralintide
Numer CAS 2883634-40-8
Synonyms LY3437943, GIP/GLP-1/glucagon receptor triagonist, Retatrutide analog
Wzór cząsteczkowy C221H343N55O68
Masa cząsteczkowa ~4970 Da
Wygląd White to off-white lyophilized powder
Czystość (HPLC) ≥98,01 TP3T
Rozpuszczalność Soluble in water and aqueous buffers (pH 4-7)
Przechowywanie -20°C, protected from light
Opakowanie 5 mg, 10 mg, 50 mg, 100 mg in glass vials

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Eloralintide Structure

Synonimy: LY3437943, GIP/GLP-1/glucagon receptor triagonist, Retatrutide analog, Triple agonist peptide

Eloralintide is a synthetic peptide engineered as a triple agonist of the glucose-dependent insulinotropic polypeptide (GIP), glucagon-like peptide-1 (GLP-1), and glucagon receptors. Its design incorporates structural motifs from native incretin hormones, with modifications to enhance stability and receptor affinity. The peptide backbone features a C-terminal amide and fatty acid side chain for prolonged half-life, making it a promising candidate for metabolic disorders.

Developed by LyvBio, Eloralintide is produced via solid-phase peptide synthesis and purified using preparative HPLC. It is supplied as a lyophilized powder with high purity, suitable for preclinical and clinical research. The compound is intended for investigation in obesity, type 2 diabetes, and non-alcoholic steatohepatitis (NASH) models.

With its unique triple agonist profile, Eloralintide offers a novel approach to modulating multiple metabolic pathways simultaneously. Researchers are exploring its potential to improve glycemic control, reduce body weight, and enhance lipid metabolism. This product is for research use only and not for human consumption.

Struktura chemiczna i właściwości

Eloralintide is a 39-amino acid peptide with a molecular weight of approximately 4970 Da. It contains non-natural amino acids and a palmitic acid moiety conjugated via a linker to lysine residues, which facilitates binding to serum albumin and extends its circulation time. The peptide is highly soluble in aqueous solutions at neutral pH and exhibits stability when stored desiccated at -20°C.

Mechanizm działania

  • GIP receptor agonism: Enhances insulin secretion in a glucose-dependent manner and may improve adipose tissue function.
  • GLP-1 receptor agonism: Suppresses glucagon release, slows gastric emptying, and promotes satiety, leading to reduced food intake.
  • Glucagon receptor agonism: Increases energy expenditure and lipolysis, contributing to weight loss and improved lipid profiles.
  • Synergistic metabolic effects: The combined activation of three receptors amplifies beneficial effects on glucose homeostasis and body weight regulation.

Specyfikacje jakościowe

Parametr Specyfikacja
Wygląd White to off-white powder
Czystość (HPLC) ≥98,01 TP3T
Peptide Content ≥80.0% (by nitrogen analysis)
Water Content ≤8.0% (Karl Fischer)
Acetate Content ≤15.0%
Trifluoroacetate Content ≤1,01 TP3T
Endotoxin ≤5 EU/mg

Dostawa i dokumentacja

  • Pojemność: 100 g per month
  • Czas realizacji: 3–5 dni roboczych (towary dostępne w magazynie)
  • Dokumentacja: COA, MSDS, TDS, HPLC chromatogram
  • Opakowanie: 5 mg, 10 mg, 50 mg, 100 mg in glass vials with desiccant

Zapytanie ofertowe

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Zapytanie ofertowe

Nasz adres

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