Eloralintide

Eloralintide

Nom du produit Eloralintide
Numéro CAS 2883634-40-8
Synonymes LY3437943, GIP/GLP-1/glucagon receptor triagonist, Retatrutide analog
Formule moléculaire C221H343N55O68
Poids moléculaire ~4970 Da
Apparence White to off-white lyophilized powder
Pureté (HPLC) ≥98,01 TP3T
Solubilité Soluble in water and aqueous buffers (pH 4-7)
Stockage -20°C, protected from light
Colis 5 mg, 10 mg, 50 mg, 100 mg in glass vials

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Eloralintide Structure

Synonymes : 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.

Structure chimique et propriétés

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.

Mécanisme d'action

  • 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.

Spécifications de qualité

Paramètre Spécifications
Apparence Poudre blanche à blanc cassé
Pureté (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

Approvisionnement et documentation

  • Capacité: 100 g per month
  • Délai de livraison: 3 à 5 jours ouvrés (articles en stock)
  • Documentation: COA, MSDS, TDS, HPLC chromatogram
  • Emballage: 5 mg, 10 mg, 50 mg, 100 mg in glass vials with desiccant

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