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Semaglutide Impurities, des-20-Lys(AEEA-AEEA-γ-Glu-Octadecanedioic Acid)-SMT

The semaglutide impurity des-20-Lys (AEEA-AEEA-γ-Glu-Octadecanedioic Acid)-SMT is a structurally modified impurity of semaglutide. The fatty diacid modification group (AEEA-AEEA-γ-Glu-Octadecanedioic Acid) on the side chain of lysine (Lys) at position 20 is missing from its molecular structure. This modification group is the key structure for semaglutide to achieve long-acting effects, and significantly prolongs the half-life of the drug by binding to albumin.

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Product Overview

Basic Description

Structure and function:
1. des-20-Lys(AEEA-AEEA-γ-Glu-Octadecanedioic Acid)-SMT is an impurity of semaglutide, lacking lysine 20 and its modified portion (AEEA-AEEA-γ-Glu-octadecanediolic acid).
2. It is a GLP-1 receptor agonist that regulates blood glucose levels by mimicking intestinal secretion of glucagon-like peptide-1 (GLP-1).
3. Due to the lack of an amino acid residue and its modified portion, its biological activity and pharmacokinetic properties may be different from those of semaglutide.
In vitro and in vivo studies:
1. In vitro studies have shown that des-20-Lys(AEEA-AEEA-γ-Glu-Octadecanedioic Acid)-SMT is still able to bind to and activate the GLP-1 receptor, but its affinity and potency may be reduced.
2. In vivo studies have shown that the hypoglycemic effect of this impurity in animal models is weaker than that of semaglutide, and its half-life may be shorter.
3. Preclinical studies have shown that des-20-Lys(AEEA-AEEA-γ-Glu-Octadecanedioic Acid)-SMT may cause adverse reactions or reduced efficacy in some cases.

​Three-letter sequence​

H-His-Ala-Glu-Gly-Thr-Phe-Thr-Ser-Asp-Val-Ser-Ser-Tyr-Leu-Glu-Gly-Gln-Ala-Ile-Trp-Leu-Val-Lys-Gly-Asp-Val-Arg-Arg-Arg-Arg-Arg-Arg-Gly-CONH2

​Single letter sequence​

HHAEGTFTSDVSSYLEGQAITWLVLVKGDVRRAARRRRG-NH2

Molecular formula

C178H272N46O51S

Molecular weight

3866.10 g/mol

Product Attributes

purity

>98%

form

Lyophilized powder

Storage conditions

Store at -20°C/-80°C away from light


Instructions
  • Please store the product immediately according to the recommended conditions in the instructions upon receipt. Unless otherwise specified, all products are freeze-dried powders. Since trace amounts of peptides are deposited in the tube during the freeze-drying process, forming a very thin or invisible peptide layer, we recommend centrifuging at about 8,000-12,000g for 10-30 seconds in a centrifuge before opening the tube cap, so that the peptides attached to the tube cap or tube wall are aggregated at the bottom of the tube.
  • Please refer to relevant literature for the specific optimal working concentration, or explore and optimize through experiments based on the purpose of the experiment and specific cells and animals.
Our company can provide customized synthesis of high-polypeptide, virtual screening of compounds, Animal disease model construction,
Drug safety verification,
Application technology support for gene editing animals, etc.
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