
GLP1-SG
Long-acting GLP-1 receptor agonist analogue for metabolic pathway studies.
GLP-1 Was the Beginning. GLP-3 Expands the Research.
For Research Use Only. Not for Human Consumption.

Triple-agonist peptide studied at the GLP-1, GIP and glucagon receptors.
GLP3-RT 10 mg
Your order ships with the certificate for its own lot. 2 earlier certificates for this size in the COA library.
Triple-agonist peptide studied at the GLP-1, GIP and glucagon receptors.
10 mg per vial, as a lyophilized powder in a sealed glass vial with a crimped cap. The lot number on the label matches the certificate of analysis in the COA library.
Store lyophilized powder frozen (−20 °C) or refrigerated, sealed and away from light. Once reconstituted, keep refrigerated (2–8 °C).
Handle in a laboratory setting using appropriate protective equipment. Consult the certificate of analysis and safety data for lot-specific information.
GLP3-RT is a 39-residue lipidated peptide studied as a triple agonist at the GLP-1, GIP and glucagon receptors. It is supplied for laboratory research into multi-receptor incretin signalling, energy expenditure and hepatic lipid metabolism.
Triple agonists combine activity at three related class B G protein-coupled receptors in one molecule: the two incretin receptors (GLP-1 and GIP) and the glucagon receptor2,3. They are engineered from a hybrid peptide backbone, with a fatty-acid side chain for albumin binding and a long half-life.
The rationale is that each receptor contributes something different. GLP-1 and GIP receptor signalling act on insulin secretion and appetite; glucagon receptor signalling raises energy expenditure and drives hepatic fat oxidation, while the incretin activity offsets glucagon's tendency to raise blood glucose3.
The balance of activity across the three receptors differs between molecules, so findings for one triple agonist do not transfer automatically to another. This research compound is not a medicine, has not been evaluated by the FDA, and is sold for laboratory research only.
Three: the GLP-1 receptor, the GIP receptor and the glucagon receptor2,3.
In research models, glucagon receptor signalling increases energy expenditure and hepatic fat oxidation; pairing it with incretin receptor activity counters glucagon's effect on blood glucose3.
10 mg, 30 mg, 48 mg and 60 mg vials of lyophilized peptide, each lot with its own certificate.
Sealed vials of lyophilized peptide are kept frozen (−20 °C) or refrigerated, dry and away from light. Peptide storage and stability explains why.
Every lot is tested by an independent laboratory for identity (mass spectrometry) and purity (HPLC). The certificate for the lot on your vial is published in the COA library and linked from this page.
Research summary reviewed 2026-10-26 against the cited literature.
Why GLP3-RT
Targets GLP-1, GIP, and glucagon receptors rather than GLP-1 alone.
Designed to investigate multiple pathways involved in energy balance and metabolic function.
Triple-receptor agonists like GLP3-RT are among the most closely watched compounds in metabolic research.
Combines three receptor mechanisms within a single investigational compound.
For Research Use Only. Not for Human Consumption.
GLP3-RT research
Move beyond single-pathway GLP-1 research and investigate the potential of multi-receptor activity.
Explore the next generation of metabolic research beyond traditional GLP-1 models.
Built for researchers exploring metabolic signaling beyond conventional GLP-1 models.
For Research Use Only. Not for Human Consumption.
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