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GLP-1 Receptor Agonist · Research Compound

SM1 (Semaglutide)

C₁₈₄H₂₉₁N₄₅O₅₉ · GLP-1 Receptor Agonist · MW 4,113.6 Da

This SM1 research guide covers its structure, mechanism, research applications and available sizes — the foundational GLP-1 receptor agonist research compound, extensively characterised and the standard reference for GLP-1 pathway research globally.

SM1 10mg research vial — Pyrox Labs
Molecular Formula
C₁₈₄H₂₉₁N₄₅O₅₉
Molecular Weight
4,113.6 Da
GLP-1 Homology
~94%
Available Sizes
5mg · 10mg · 20mg Bundle
Modification
C18 Fatty Diacid
Research Overview

What Is SM1?

SM1 is a synthetic analogue of native human GLP-1 (Glucagon-Like Peptide-1), sharing approximately 94% amino acid sequence homology with the endogenous hormone. It incorporates a C18 fatty diacid modification attached via a hydrophilic linker at position 26, enabling strong albumin binding and dramatically extending its half-life compared to native GLP-1.

Native GLP-1 has a half-life of only 1–2 minutes due to rapid degradation by the enzyme DPP-4 (dipeptidyl peptidase-4), as documented in peer-reviewed pharmacology literature. Its structural modifications — including a substitution at position 8 that confers DPP-4 resistance — extend the compound's half-life to approximately 7 days in relevant models, making it far more practical for extended laboratory protocols.

SM1 is the most extensively published GLP-1 receptor agonist compound in the scientific literature, making it the essential reference compound for any GLP-1 pathway research programme. It is available from Pyrox Labs in 5mg and 10mg individual research vials.

Research Use Only: SM1 is supplied by Pyrox Labs exclusively for in vitro laboratory research and independent scientific study. Not for human consumption, self-administration or therapeutic use.

Structural Modifications

Three key structural modifications distinguish it from native GLP-1 and contribute to its extended half-life and receptor binding characteristics:

🔗
C18 Fatty Diacid
A C18 fatty diacid chain attached via a hydrophilic linker enables reversible albumin binding, dramatically slowing renal clearance and extending half-life. This lipidation strategy is now standard across next-generation GLP-1 class research compounds.
🛡️
DPP-4 Resistance
A substitution at position 8 (Aib substitution) confers resistance to DPP-4 enzyme degradation — the primary mechanism responsible for rapid native GLP-1 breakdown. Without this modification, native GLP-1 is cleared within minutes of exposure.
🧬
Arginine Substitution
Substitution at position 34 (lysine to arginine) provides the attachment site for the fatty acid modification without disrupting receptor binding affinity, keeping the conjugate clear of the receptor-binding surface.

GLP-1 Receptor Pathway

It acts as a full agonist at the GLP-1 receptor (GLP-1R), a class B G protein-coupled receptor. GLP-1R activation triggers cyclic AMP (cAMP) signalling cascades with downstream effects in multiple tissues. Key research areas include pancreatic beta cell signalling, gastric motility modulation, hypothalamic appetite-regulating pathways and cardiovascular function in relevant research models. Downstream ERK1/2 and PKA signalling cascades are also commonly used as functional readouts in receptor activation assays.

Research Applications

SM1 Research Guide — Applications

🔬
Pancreatic Research
GLP-1 receptor expression in pancreatic beta cells. Glucose-dependent insulin signalling pathway research.
🧠
CNS & Appetite
Hypothalamic and brainstem GLP-1 receptor expression. Neuroendocrine appetite regulation pathway research.
🫀
Cardiovascular
Cardiac and vascular GLP-1 receptor expression. Cardiometabolic pathway research in relevant models.
⚗️
Gastric Motility
GLP-1 mediated gastric emptying rate modulation and gastrointestinal receptor signalling research.
📊
Reference Standard
Its extensive published literature makes it the essential GLP-1 reference compound for comparative research protocols.
🧬
Hepatic Function
Liver GLP-1 receptor pathway research including lipid metabolism and hepatic glucose output modulation studies.
Available From Pyrox Labs

Sizes & Pricing

This SM1 research guide includes full sizing and reconstitution details below. It's available in individual research vials and as part of a 20mg research bundle. All pricing subject to confirmation.

SM1 5mg
Single research vial · Lyophilised · COA available
Was £29.99
£21.99
Buy Now
SM1 10mg
Single research vial · Lyophilised · COA available
Was £39.99
£31.50
Buy Now
SM1 20mg Bundle SAVE
2 x 10mg vials · Best value for extended protocols
Was £89.99
£49.99
Buy Now

Storage & Reconstitution

Store the lyophilised compound at room temperature away from direct light and moisture. Once reconstituted with bacteriostatic water, store refrigerated at 2–8°C and use within 28 days. Do not freeze reconstituted solution. It reconstitutes clearly — any cloudiness or particulate matter after thorough swirling may indicate degradation.

Full Reconstitution Guide →

Research Use Only: SM1 supplied by Pyrox Labs is intended exclusively for in vitro laboratory research and independent scientific study. Not a licensed medicine. Not for human consumption, self-administration or therapeutic use. Pyrox Labs provides no medical advice.

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