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Survodutide

2 - 500 pieces$90.00

数量

最小起订量为: 2 pieces
piece
小计
$180.002 × $90.00

运输

供应商将在 3–10 天内发货 (付款确认后)

货物将从 United Kingdom, China 港口发出。

运输采用 FOB 条款——供应商承担至指定装运港的费用。

提供样品 · $250.00/每件样品

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Meet your supplier

CorePepts L
CorePepts L

Distributor / Wholesaler • 3 yr United Kingdom UNITED KINGDOM

56%

On-time delivery rate

≤24h

Response Time

75

Employee Size

$500K

Annual Revenue

588

Products Sold

Location

United KingdomBelfast, 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.

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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.
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  • 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

2805997-46-8

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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