The GLP-1 Class: Semaglutide, Tirzepatide, and Retatrutide Research

Class research profile

The GLP-1 Class — Semaglutide, Tirzepatide, and Retatrutide

Three generations of incretin-based research peptides. Single, dual, and triple receptor agonists. Compared head-to-head on mechanism, peer-reviewed outcomes, and analytical purity. HPLC-verified, COAs on every lot.

Compare All Three | Read Peer-Reviewed Citations


TL;DR. The GLP-1 class includes Semaglutide, Tirzepatide, and Retatrutide, each studied in peer-reviewed GLP-1, GIP, and glucagon receptor research. Improved Peptides supplies these compounds for in vitro and laboratory research only — not for human consumption — with third-party COAs.

What is the GLP-1 class?

The GLP-1 class is a family of synthetic peptide research compounds that act as agonists at the glucagon-like peptide-1 (GLP-1) receptor. The class has expanded across three generations, each broadening the receptor scope:

GenerationCompoundReceptor scopeYear of first synthesis
1stSemaglutideGLP-1 receptor (single)2012
2ndTirzepatideGLP-1 + GIP (dual)2018
3rdRetatrutideGLP-1 + GIP + Glucagon (triple)2022

Each compound has been studied in peer-reviewed Phase 2 and Phase 3 trials for metabolic and incretin-pathway research. Improved Peptides supplies all three for in vitro and laboratory research only — not for human consumption.


Side-by-side comparison

DimensionSemaglutideTirzepatideRetatrutide
ClassGLP-1 single agonistGLP-1/GIP dual agonistGLP-1/GIP/Glucagon triple agonist
Half-life~165 hours (~7 days)~120 hours (~5 days)~150 hours (~6 days)
Mechanism scopeGLP-1 onlyGLP-1 + GIPGLP-1 + GIP + Glucagon
Phase status (2026)Approved (Wegovy/Ozempic in clinical settings)Approved (Mounjaro/Zepbound in clinical settings)Phase 3 ongoing
Notable Phase 2 outcomeSTEP/SELECT/SUSTAIN trial programSURPASS/SURMOUNT trial programPhase 2 body-composition outcomes published in 2023 (Jastreboff et al., NEJM)
Research interest trendPlateau — well-characterizedRising — extensive recent literatureSteep rise — newest, most actively studied
Improved Peptides purityHPLC 99%+HPLC 99%+HPLC 99%+
Product pageShop SemaglutideShop TirzepatideShop Retatrutide
Research profileSemaglutide researchTirzepatide researchRetatrutide research

Mechanism deep dive

Semaglutide — GLP-1 single agonism

Semaglutide is a long-acting analog of human GLP-1 with a fatty-acid side chain that extends its plasma half-life via albumin binding. It binds selectively to the GLP-1 receptor, modulating glucose-dependent insulin secretion, gastric emptying, and central appetite signaling pathways studied in incretin research.

Tirzepatide — GLP-1 + GIP dual agonism

Tirzepatide is a 39-amino-acid synthetic peptide engineered to activate both the GLP-1 and GIP (glucose-dependent insulinotropic polypeptide) receptors. The dual-agonist design has been studied for additive effects on insulin sensitivity, lipolysis, and energy expenditure beyond GLP-1 monotherapy.

Retatrutide — GLP-1 + GIP + Glucagon triple agonism

Retatrutide is the third-generation tri-agonist, adding glucagon receptor activity to the GLP-1/GIP combination. Glucagon-receptor signaling has been studied for its role in hepatic energy metabolism and basal metabolic rate. Phase 2 data (Jastreboff et al., 2023) reported the largest body-composition changes observed across the class.


Citations (peer-reviewed, PubMed-linked)

Semaglutide

  1. Marso SP, et al. “Semaglutide and Cardiovascular Outcomes (SUSTAIN-6).” NEJM. 2016. PMID: 27633186
  2. Wilding JPH, et al. “Once-Weekly Semaglutide in Adults with Overweight or Obesity (STEP 1).” NEJM. 2021. PMID: 33567185
  3. Davies M, et al. “Semaglutide 2.4 mg once a week in adults with overweight or obesity, and type 2 diabetes (STEP 2).” Lancet. 2021. PMID: 33667417
  4. Lincoff AM, et al. “Semaglutide and Cardiovascular Outcomes in Obesity without Diabetes (SELECT).” NEJM. 2023. PMID: 37952131

Tirzepatide

  1. Frias JP, et al. “Tirzepatide versus Semaglutide Once Weekly (SURPASS-2).” NEJM. 2021. PMID: 34170647
  2. Jastreboff AM, et al. “Tirzepatide Once Weekly for the Treatment of Obesity (SURMOUNT-1).” NEJM. 2022. PMID: 35658024
  3. Rosenstock J, et al. “Efficacy and safety of tirzepatide monotherapy (SURPASS-1).” Lancet. 2021. PMID: 34186022
  4. Karagiannis T, et al. “Tirzepatide vs other GLP-1 RAs: systematic review and meta-analysis.” BMJ. 2022. PMID: 35338814

Retatrutide

  1. Jastreboff AM, et al. “Triple-Hormone-Receptor Agonist Retatrutide for Obesity — Phase 2.” NEJM. 2023. PMID: 37354450
  2. Rosenstock J, et al. “Retatrutide, a GIP/GLP-1/glucagon receptor agonist, in adults with type 2 diabetes.” Lancet. 2023. PMID: 37356449
  3. Sanyal AJ, et al. “Retatrutide for metabolic dysfunction-associated steatotic liver disease.” Lancet GH. 2024. PMID: 38663433

Quality and verification

Every batch of Semaglutide, Tirzepatide, and Retatrutide is independently tested by a third-party laboratory using:

  • HPLC — for purity (target 99%+)
  • Mass spectrometry — for sequence confirmation
  • UV spectroscopy — for concentration verification

Current batch COAs are published in our COA Library and linked from each product page. Every lot is traceable.


Storage and reconstitution (research reference)

StageCondition
Lyophilized vial (shipping)Room temperature, stable for 2-3 weeks
Lyophilized vial (long-term)Refrigerator (2-8°C) for 6-12 months; freezer (-20°C) for 24+ months
Reconstituted (with bacteriostatic water)Refrigerated, use within 28 days

Reconstitution solvent: Bacteriostatic water with 0.9% benzyl alcohol. Available at /shop/bacteriostatic-water/.


Choosing between the three (research framework)

Researchers selecting between Semaglutide, Tirzepatide, and Retatrutide typically evaluate four axes:

  1. Mechanism scope: Single (Sema) → Dual (Tirz) → Triple (Reta) receptor activation
  2. Published outcome magnitude: Phase 2 body-composition data trends Reta > Tirz > Sema
  3. Research history: Sema has the longest published record; Reta has the newest
  4. Cost-per-mg: Sema lowest, Reta highest at current market rates

The choice depends on the research question being investigated. All three are stocked, HPLC-verified, and ship same-day on orders before 2pm ET.


FAQ

Q: What is the GLP-1 class?
A: A family of synthetic peptide research compounds that activate the GLP-1 receptor. The class has expanded to include dual (GLP-1/GIP) and triple (GLP-1/GIP/Glucagon) receptor agonists.

Q: What is the difference between Semaglutide, Tirzepatide, and Retatrutide?
A: Semaglutide is a single GLP-1 agonist. Tirzepatide is a dual GLP-1 + GIP agonist. Retatrutide is a triple GLP-1 + GIP + Glucagon agonist. They differ in receptor scope, half-life, and the breadth of peer-reviewed published research.

Q: Where do I find peer-reviewed citations?
A: Citations for all three compounds are listed in the section above with direct PubMed links. We update the citation list as new peer-reviewed research is published.

Q: What purity standard does Improved Peptides verify?
A: HPLC-tested 99%+ purity, sequence-confirmed by mass spectrometry, with a COA from an independent third-party lab on every batch.

Q: Are these peptides legal to purchase?
A: All compounds offered by Improved Peptides are sold strictly for in vitro and laboratory research use. They are not for human consumption, diagnosis, or treatment.

Q: Which GLP-1 compound has the most published research?
A: Semaglutide currently has the longest and most extensive published record, with Tirzepatide rapidly expanding. Retatrutide is the newest and has the most active research pipeline.

Q: How is the Wolverine Stack different from the GLP-1 class?
A: The Wolverine Stack is a tissue-repair research combination (BPC-157 + TB-500). The GLP-1 class is a metabolic/incretin research family. Different mechanisms, different research applications.


Ready to source the GLP-1 class?

All three compounds — Semaglutide, Tirzepatide, and Retatrutide — are stocked, HPLC-tested, and ship same-day on orders before 2pm ET.

Shop Semaglutide | Shop Tirzepatide | Shop Retatrutide | View All Class Components

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