Survodutide
Meet your supplier

Distributor / Wholesaler • 3 yr •
UNITED KINGDOM
56%
On-time delivery rate
≤24h
Response Time
75
Employee Size
$500K
Annual Revenue
588
Products Sold
Location
Belfast, United Kingdom
Survodutide (BI 456906) is a novel dual agonist of the glucagon-like peptide-1 (GLP-1) and glucagon (GCGR)receptors. Its key features center on its ability to simultaneously target appetite and liver function for metabolic improvements.
+1
Clinical & Therapeutic Features
- Significant Weight Loss: In Phase III SYNCHRONIZE-1 trials, participants without type 2 diabetes achieved an average body weight reduction of up to 16.6% over 76 weeks.
- Dual Mechanism of Action: It combines GLP-1 agonism, which reduces appetite and increases satiety, with glucagon agonism, which directly acts on the liver to enhance energy expenditure and fat metabolism.
- Metabolic Health Marker Improvement: Treatment has led to significant reductions in waist circumference, a key indicator of visceral fat and cardiometabolic risk.
- Liver Disease Targeting: Because it activates glucagon receptors in the liver, it is being studied for its ability to reduce hepatic fat, resolve inflammation, and improve fibrosis in patients with MASH (Metabolic Dysfunction-Associated Steatohepatitis).
- Long-Acting Profile: It has a plasma half-life of approximately 6 days, supported by a high binding affinity to human serum albumin (>99%), allowing for once-weekly dosing.
Technical Overview
- Mechanism of Action: It acts as a unimolecular dual agonist that simultaneously activates GLP-1 receptors to reduce food intake and improve glucose tolerance, while activating glucagon receptors to increase energy expenditure and promote fat metabolism in the liver.
- Structure: A 29-amino-acid linear synthetic peptide acylated with a C18 fatty diacid moiety. This acylation enables high binding affinity to human serum albumin (>99%), extending its plasma half-life to approximately 6 days for once-weekly dosing.
+1 - Potency (EC50): In CHO-K1 cell assays, its functional potency is approximately 0.33 nM for the GLP-1 receptor and 0.52 nM for the glucagon receptor.
Technical Specifications
|
Feature |
Data |
|
CAS Number |
|
|
Molecular Formula |
C₁₉₂H₂₈₉N₄₇O₆₁ |
|
Molecular Weight |
4231.7 g/mol |
|
Sequence |
H-His-{Ac4c}-Gln-Gly-Thr-Phe-Thr-Ser-Asp-Tyr-Ser-Lys-Tyr-Leu-Asp-Glu-Arg-Ala-Ala-Lys-Asp-Phe-Ile-{diacid-C18-gamma-Glu-Gly-Ser-Gly-Ser-Gly-Gly-Lys}-Trp-Leu-Glu-Ser-Ala-NH₂ |
|
Appearance |
White powder |
|
Storage |
Powder: -20°C for up to 3 years |
Logistics & Customs Data
- HS / Custom Code: 2937.19.00. This code covers polypeptide and protein hormones, their derivatives, and structural analogues.
- Regulatory Category: Typically classified as a Laboratory Reagent or for Research Use Only (RUO) to facilitate international shipping for laboratory studies.
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