Survodutide

Survodutide

Nom du produit Survodutide
Numéro CAS 2805997-46-8
Formule moléculaire C192H296N48O57
Poids moléculaire 4267.7 g/mol
Apparence White to off-white lyophilized powder
Pureté (HPLC) ≥98,01 TP3T
Solubilité Soluble in water and aqueous buffers
Stockage Store at -20°C, protected from light
Colis 1 mg, 5 mg, 10 mg, 50 mg, 100 mg, 500 mg, 1 g

Besoin d'aide ? Contacter notre équipe

Survodutide Structure

Synonymes : Survodutide, BI 456906, Glucagon/GLP-1 receptor dual agonist, GCGR/GLP-1R co-agonist

Survodutide is a synthetic peptide engineered as a dual agonist of the glucagon receptor (GCGR) and glucagon-like peptide-1 receptor (GLP-1R). It belongs to a new generation of incretin-based therapeutics designed to address metabolic disorders through simultaneous activation of two complementary pathways. Originally developed by Boehringer Ingelheim, survodutide has drawn significant interest for its potential in obesity and non-alcoholic steatohepatitis (NASH).

Structurally, survodutide is a 29-amino acid peptide with a C-terminal extension and a fatty acid side chain that promotes albumin binding and extends its half-life. This modification allows for once-weekly subcutaneous dosing. The dual agonism leverages GLP-1 receptor activation to suppress appetite and improve glycemic control, while glucagon receptor activation increases energy expenditure and promotes hepatic lipid oxidation, offering a multi-pronged approach to weight management and liver health.

In clinical trials, survodutide has demonstrated robust reductions in body weight and improvements in liver fibrosis markers, positioning it as a promising candidate for the treatment of metabolic dysfunction-associated steatohepatitis (MASH). As the demand for effective therapies grows, survodutide represents a critical tool for researchers and pharmaceutical companies focused on metabolic diseases.

Fonction

  • Dual receptor agonism: Simultaneously activates GCGR and GLP-1R, enhancing metabolic effects.
  • Réduction de l'appétit: GLP-1R activation reduces food intake and promotes satiety.
  • Increased energy expenditure: GCGR activation stimulates thermogenesis and lipid oxidation.
  • Glycemic control: Improves insulin sensitivity and glucose homeostasis.
  • Hepatic steatosis reduction: Promotes fat breakdown in the liver, addressing NASH.

Source et normalisation

  • Source: Peptide synthétique obtenu par synthèse peptidique en phase solide.
  • Normalisation: ≥98% purity by HPLC; identity confirmed by mass spectrometry.
  • Formulaires: Lyophilized powder for reconstitution.
  • Applications: Research on obesity, diabetes, NASH, and metabolic syndrome.

Caractéristiques techniques

Paramètre Spécifications
Essai (HPLC) ≥98,01 TP3T
Identification Mass spectrometry conforms
Peptide Content ≥80.0%
Water Content ≤8.0%
Métaux lourds ≤ 10 ppm
Limites microbiologiques Total aerobic count ≤100 CFU/mg

Documentation et approvisionnement

  • Capacité mensuelle: 100 g
  • Délai de livraison: 3 à 5 jours ouvrés (articles en stock)
  • Documentation: COA, MSDS, TDS, HPLC, MS
  • Emballage: Lyophilized powder in sealed vials

Demande de devis

RESTEZ EN CONTACT

Demande de devis

Notre adresse

Room,5-0203, Unit 5, Beiyuanmen Street,Xi'an,Shaanxi,China

✅ ×