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IRONXPEPTIDES
SEMAGLUTIDE 2MG research vial, Iron Peptide Research label
Metabolic & Incretin

Semaglutide

Also known as NN9535

Semaglutide is a long-acting analogue of human GLP-1. It is one of the most extensively studied incretin-based compounds, with large trials in type 2 diabetes, obesity, and cardiovascular outcomes.

Approved drug substance

Size

6 options
Catalog no.
SM2
Specification
2mg *10vials
Per kit
10 vials
PricePricing will be published soon

For laboratory research use only. Not for human or animal consumption. Buyers must be 21 or older.

Overview

Semaglutide was developed by Novo Nordisk and shares 94% of its amino acid sequence with human GLP-1. An Aib substitution at position 8 resists breakdown by the enzyme DPP-4, and arginine at position 34 leaves lysine 26 as the attachment site for a C18 fatty diacid side chain. That side chain binds albumin, giving a half-life of about one week in humans. Semaglutide is approved for type 2 diabetes, chronic weight management, and cardiovascular risk reduction in defined populations. The SUSTAIN, PIONEER, and STEP programs and the SELECT outcomes trial make up much of the published evidence.

Class: GLP-1 receptor agonist

Mechanism of action

How the compound acts, as described in the literature.

  1. Activates the GLP-1 receptor, a G protein-coupled receptor that signals mainly through cAMP. Its receptor affinity is about threefold lower than that of liraglutide, offset by much longer circulation.

  2. In pancreatic islets it increases glucose-dependent insulin secretion and lowers glucagon secretion, so its glucose-lowering effect diminishes as glucose approaches normal levels.

  3. Slows gastric emptying and acts on GLP-1 receptors in the hypothalamus and hindbrain to reduce appetite and food intake.

  4. Outcome trials reported fewer major cardiovascular events. Proposed contributors include changes in weight, blood pressure, lipids, and inflammation, but the mechanisms are not settled.

Published research

Selected studies, each linked to its PubMed record. Summaries describe what the studies reported.

Evidence & safety

What the research does not show, and the adverse events and regulatory status it reports.

Nausea and diarrhea were the most common adverse events in STEP 1, and 4.5% of semaglutide participants stopped treatment because of gastrointestinal events versus 0.8% with placebo; in SELECT, discontinuation for adverse events was 16.6% versus 8.2%. In SUSTAIN-6, diabetic retinopathy complications were significantly more frequent with semaglutide than with placebo. US labeling carries a boxed warning based on thyroid C-cell tumors seen in rodents.

Specifications

All sizes, exactly as catalogued.

Catalog no.ProductSpecificationVials per kit
SM2Semaglutide2mg *10vials10
SM5Semaglutide5mg *10vials10
SM10Semaglutide10mg *10vials10
SM15Semaglutide15mg *10vials10
SM20Semaglutide20mg *10vials10
SM30Semaglutide30mg *10vials10

For laboratory research use only. Not for human or animal consumption. Not intended to diagnose, treat, cure or prevent any disease. Research summaries are provided for educational purposes and do not describe this product’s use.

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