Buy GLP-2 TZ Dual GIP/GLP-1 Research Peptide | Koi Aminos
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GLP-2 TZ research peptide
Lyophilized powder

GLP-2 TZ Tirzepatide-Class Research Peptide

Tirzepatide Class · Dual GIP/GLP-1 Agonist

GLP-2 TZ is the dual-agonist bridge in the GLP-1 class - it hits GIP and GLP-1 receptors simultaneously, positioning between semaglutide (GLP-1R only) and GLP-3 RT (GLP-1R + GIPR + GCGR).

Size: 10mg

$89.95/ 10mg≥99% HPLC

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For Research Use Only. Not for human or animal use. Not intended to diagnose, treat, cure, or prevent any disease. Sold exclusively for laboratory and analytical research purposes.

CAS Number

2023788-19-2

Molecular Weight

4813.50 g/mol

Semaglutide only hits GLP-1R. That one-receptor view misses the second half of incretin pharmacology - the glucose-dependent insulinotropic polypeptide receptor (GIPR), which plays its own role in insulin secretion, lipid metabolism, and energy balance. You need the dual-agonist pharmacological profile to study what adding GIPR actually changes.

GLP-2 TZ is a tirzepatide-class synthetic dual GIP/GLP-1 receptor agonist - the first compound class to simultaneously activate both GIPR and GLP-1R. CAS 2023788-19-2, MW 4813.50 g/mol. Its dual incretin activation profile positions it between single-agonist GLP-1 compounds and triple agonists like GLP-3 RT (Retatrutide), making it the essential intermediate reference in GLP-1 class comparative pharmacology research.

We supply GLP-2 TZ at ≥99% HPLC purity in 10mg, 15mg, and 30mg vials with a lot-specific COA. For in vitro laboratory research use only.

Key Takeaways

First compound class to simultaneously activate GIPR and GLP-1R - the dual-receptor incretin twincretin mechanism
Pharmacological bridge: above semaglutide (GLP-1R only), below GLP-3 RT (triple agonist) - the indispensable middle reference
CAS 2023788-19-2, MW 4813.50 g/mol; ≥99% HPLC purity with COA online
3 sizes - 10mg, 15mg, and 30mg - for protocol flexibility from pilot to full dose-response
Order alongside GLP-3 RT to run dual-vs-triple receptor comparison studies from the same supplier

Key Scientific Specifications

Dual GIP/GLP-1 receptor agonism - simultaneous GIPR + GLP-1R activation; tirzepatide compound class
CAS 2023788-19-2 · MW 4813.50 g/mol · ≥99% purity by HPLC; LC-MS identity confirmed; acetate salt
Lot-specific COA: HPLC purity, LC-MS identity, net content
Three sizes: 10mg, 15mg, 30mg - all lyophilized powder
Pharmacological bridge between semaglutide (GLP-1R) and GLP-3 RT (GLP-1R + GIPR + GCGR) for step-up receptor research

Research-Referenced Attributes

Based on published preclinical and clinical literature; not therapeutic claims. For laboratory research use only.

Dual incretin pharmacology: simultaneous GIPR + GLP-1R activation - study the incretin synergy unavailable with semaglutide (GLP-1R only)
Comparative receptor pharmacology reference: dual-agonist mid-point between single (semaglutide) and triple agonist (GLP-3 RT) profiles
Glucose homeostasis and insulin secretion models: GIPR contribution to post-prandial insulin response alongside GLP-1R signaling
Lipid metabolism and adipose tissue biology research: GIPR-driven effects on lipogenesis and lipolysis in adipocyte models
Energy balance research: comparing dual-agonist vs. triple-agonist energy expenditure profiles in preclinical models
Cardiovascular outcome research: incretin receptor activation and cardiometabolic risk marker modulation studies

Also in This Research Area

Researchers working with GLP-2 TZ frequently also order GLP-3 RT triple agonist for extending dual-receptor studies to include GCGR activation, and AOD-9604 (hGH fragment 176–191) for β3-adrenergic and incretin pathway comparison. Both are available as lyophilized research-grade peptides on the Koi Aminos research peptide marketplace.