Survodutide

Survodutide

제품명 Survodutide
CAS 번호 2805997-46-8
분자식 C192H296N48O57
분자량 4267.7 g/mol
외관 White to off-white lyophilized powder
순도 (HPLC) ≥98.0%
용해도 Soluble in water and aqueous buffers
저장 Store at -20°C, protected from light
패키지 1 mg, 5 mg, 10 mg, 50 mg, 100 mg, 500 mg, 1 g

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Survodutide Structure

동의어: 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.

Function

  • Dual receptor agonism: Simultaneously activates GCGR and GLP-1R, enhancing metabolic effects.
  • Appetite suppression: 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

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

사양

매개변수 사양
분석법 (HPLC) ≥98.0%
식별 Mass spectrometry conforms
Peptide Content ≥80.0%
Water Content ≤8.0%
중금속 ≤10 ppm
Microbial Limits Total aerobic count ≤100 CFU/mg

Documentation & Supply

  • Monthly capacity: 100 g
  • 리드 타임: 3-5 business days (stock items)
  • 문서: COA, MSDS, TDS, HPLC, MS
  • 포장: Lyophilized powder in sealed vials

견적 요청

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견적 요청

주소

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

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