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Semaglutide Impurities, des-20-4-Octadecanedioic Acid-SMT

The semaglutide impurity des-20-4-Octadecanedioic Acid-SMT is a key structural defect impurity that may be generated during the synthesis or storage of semaglutide (an acylated GLP-1 analog used to treat type 2 diabetes and obesity). The impurity is characterized by the absence of the octadecanedioic acid (Octadecanedioic Acid) side chain at position 20 in the molecule, which may lead to changes in the drug's lipophilicity, decreased plasma albumin binding ability, and shortened half-life.

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Product Overview

Basic Description

Structure and function:
1. des-20-4-Octadecanedioic Acid-SMT is an impurity of semaglutide that lacks the fourth moiety of octadecanedioic acid modification at position 20 of lysine.
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 a modified moiety, its biological activity and pharmacokinetic properties may differ from those of semaglutide.
In vitro and in vivo studies:
1. In vitro studies have shown that des-20-4-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-20-4-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-Lys(AEEA-AEEA-γ-Glu)-Ile-Trp-Leu-Val-Lys-Gly-Asp-Val-Arg-Arg-Arg-Arg-Arg-Arg-Gly-CONH2

​Single letter sequence​

HHAEGTFTSDVSSYLEGQAK(AEEA-AEEA-γ-Glu)ITWLVLVKGDVRRAARRRRG-NH2

Molecular formula

C185H290N50O57S

Molecular weight

4062.17 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,
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