Survodutide

Survodutide

製品名 Survodutide
CAS番号 2805997-46-8
分子式 C192H296N48O57
分子量 4267.7 g/mol
外観 白色からオフホワイト色の凍結乾燥粉末
純度(HPLC) ≥98.0%
溶解度 水および水性緩衝液に溶解する
ストレージ Store at -20°C, protected from light
パッケージ 1 mg, 5 mg, 10 mg, 50 mg, 100 mg, 500 mg, 1 g

Survodutide Structure

同義語: 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.

機能

  • Dual receptor agonism: Simultaneously activates GCGR and GLP-1R, enhancing metabolic effects.
  • 食欲抑制: 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 & Standardization

  • 出典: Synthetic peptide produced by solid-phase peptide synthesis.
  • Standardization: ≥98% purity by HPLC; identity confirmed by mass spectrometry.
  • Forms: Lyophilized powder for reconstitution.
  • 用途: Research on obesity, diabetes, NASH, and metabolic syndrome.

仕様

パラメータ 仕様
分析(HPLC) ≥98.0%
識別 Mass spectrometry conforms
ペプチド含有量 ≥80.0%
水分含有量 ≤8.0%
重金属 10 ppm以下
Microbial Limits Total aerobic count ≤100 CFU/mg

資料・供給

  • 月間処理能力: 100 g
  • リードタイム: 3~5営業日(在庫品)
  • ドキュメント: COA, MSDS, TDS, HPLC, MS
  • パッケージ: Lyophilized powder in sealed vials

見積依頼

  • リブバイオ株式会社. — メールアドレス: info@lyvbio.com

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