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NORTHVERITY / SM30

Semaglutide

30 mg × 10 vials

For laboratory procurement

Semaglutide 30 mg × 10 vials · SM30 · Catalog illustration—not an actual packaging photo.
Catalog illustration—not an actual packaging photo.
Procurement details
Catalog number
SM30
Listed specification
30 mg
Vials per pack
10 vials
Current supply lot
Lot documents with your quote

Compound profile

Semaglutide is a 31-residue GLP-1 analogue with amino acid substitutions and a lysine-linked C18 fatty diacid side chain.

Identity

Sequence
H-H[Aib]EGTFTSDVSSYLEGQAA[K(γE-2xOEG-C18 diacid)]EFIAWLVRGRG-OH
Residues
31
Molecular formula
C187H291N45O59
Average molecular weight
4114 g/mol
Monoisotopic mass (calculated)
4111.1154 Da
CAS number
910463-68-2
PubChem CID
56843331
Strengths
5–30 mg
Other names
NN9535 · NNC 0113-0217

Lys26, using GLP-1 numbering, carries a C18 fatty diacid joined through γ-glutamic acid and two 8-amino-3,6-dioxaoctanoic acid units, abbreviated OEG.

Identity data from: PubChem CID 56843331

Residue diagram of Semaglutide
Drawn from the verified identity data on this page.

Research overview

Semaglutide is a modified analogue of glucagon-like peptide-1, or GLP-1, with a recorded chain of 31 amino acid residues. The discovery paper identifies two substitutions relative to the parent sequence, Aib at position 8 and arginine at position 34, using GLP-1 numbering [1]. A lysine at position 26 carries a fatty diacid side chain. The structure given here contains a C18 diacid connected through γ-glutamic acid and two OEG units; the chain retains a free amino terminus and a carboxyl terminus [1]. OEG denotes 8-amino-3,6-dioxaoctanoic acid within this linker [1].

The cited chemistry study examined how fatty acid and linker design influenced albumin binding and interaction with the GLP-1 receptor. Its design program considered albumin affinity alongside resistance to metabolic degradation [1]. The study also characterized the compound in mini-pigs, measuring plasma half-life and mean residence time as part of its analysis of the molecule’s persistence [1].

A later review describes reversible albumin binding in the development of modified GLP-1 analogues, with fatty acid and linker combinations selected while maintaining receptor activity [2]. It also examines cellular targets and receptor distribution. The tissues listed as expressing the GLP-1 receptor include the pancreas, gastrointestinal tract, heart, lungs, kidneys and brain [2].

Laboratory storage and handling

Store the closed container cold, dry and protected from light under the conditions specified for the lot. Let it reach room temperature before opening to limit condensation. Avoid repeated freezing and thawing of laboratory stocks. Record storage history and lot identity alongside experiments, and use standard laboratory protective equipment when handling the material.

Questions about Semaglutide

Which sequence substitutions distinguish Semaglutide?

The discovery paper identifies Aib at position 8 and arginine at position 34 relative to the parent GLP-1 sequence, using GLP-1 numbering [1].

What is attached to the lysine side chain?

Lys26 carries a C18 fatty diacid through γ-glutamic acid and two OEG units. The attachment is a structural modification of the peptide itself.

Is albumin part of Semaglutide's peptide chain?

Albumin is not a residue in the recorded chain. The cited review describes reversible binding to albumin, separate from the covalently attached fatty diacid side chain [2].

References

  1. Discovery of the Once-Weekly Glucagon-Like Peptide-1 (GLP-1) Analogue Semaglutide. J Med Chem 2015. PMID 26308095
  2. The Discovery and Development of Liraglutide and Semaglutide. Front Endocrinol (Lausanne) 2019. PMID 31031702

Identity data checked on 2026-09-24. Literature summaries describe published research models and are not specifications of any product lot.

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5 catalog entries

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