Tirzepatide
FDA-approvedFDA-approved dual GIP/GLP-1 receptor agonist
Also known as: Mounjaro, Zepbound, LY3298176
Tirzepatide is an FDA-approved dual GIP and GLP-1 receptor agonist for type 2 diabetes and weight management, producing larger average weight reduction than GLP-1-only agents in trials.
Molecular & research data
- Sequence
- Acylated GIP-based dual agonist (39-residue analog, C20 diacid linker)
- CAS number
- 2023788-19-2
- Molecular formula
- C225H348N48O68
- Molecular weight
- 4813.5 g/mol
- Half-life
- ≈5 days (~120 hours)
- Primary targets
- GIP receptor, GLP-1 receptor
- Routes (research)
- Subcutaneous
- Storage
- Refrigerate 2–8 °C; commercial pens have specific in-use limits.
Overview
Tirzepatide is a dual incretin agonist, activating both the GIP and GLP-1 receptors in a single molecule. Approved by the FDA for type 2 diabetes (Mounjaro) and chronic weight management (Zepbound), it represents the next step beyond GLP-1-only agents like Semaglutide and has set new benchmarks for weight reduction in clinical trials.
Mechanism of action
Tirzepatide engages two complementary incretin pathways:
- GLP-1 receptor — enhances glucose-dependent insulin secretion, slows gastric emptying, and reduces appetite (the same axis as semaglutide).
- GIP receptor — glucose-dependent insulinotropic polypeptide signalling, which appears to add further benefits to insulin sensitivity and energy balance when combined with GLP-1 activity.
Like semaglutide, it carries a fatty-acid chain that binds albumin to resist enzymatic breakdown, giving it a half-life of roughly five days and once-weekly dosing.
The dual mechanism is the central reason tirzepatide and semaglutide are the headline comparison in metabolic peptide research.
Common research uses
- Type 2 diabetes management (approved)
- Chronic weight management (approved)
- Comparative metabolic research against GLP-1 monoagonists
- Investigation of GIP’s contribution to metabolic outcomes
Compare Tirzepatide
Tirzepatide FAQ
What makes tirzepatide a "dual agonist"?+
It activates two incretin receptors at once — GIP and GLP-1 — whereas semaglutide activates only GLP-1. Combining both pathways is thought to enhance the metabolic and weight effects.
What is tirzepatide approved for?+
It is FDA-approved for type 2 diabetes (Mounjaro) and for chronic weight management (Zepbound).
Is tirzepatide more effective than semaglutide for weight loss?+
In head-to-head and comparable trials, tirzepatide has produced greater average weight reduction, though individual response and tolerability vary.
References
Related peptides
Semaglutide
FDA-approvedFDA-approved GLP-1 receptor agonist
Semaglutide is an FDA-approved GLP-1 receptor agonist for type 2 diabetes and chronic weight management, engineered with fatty-acid acylation for a once-weekly half-life.
Tesamorelin
FDA-approvedFDA-approved stabilised GHRH analog
Tesamorelin is a stabilised GHRH analog and the only growth-hormone secretagogue with FDA approval specifically for reducing excess visceral fat (in HIV-associated lipodystrophy).
Last reviewed: 2026-06-26. Information is provided for research and educational reference only — see our disclaimer.