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Retatrutide vs mazdutide vs survodutide: what is the difference?

Three lab-made peptides that get named together. Two of them switch on two hormone receptors. Retatrutide switches on three. Here is where each one came from and what the papers looked at.

3
Receptors retatrutide switches on
2
Receptors mazdutide and survodutide switch on
19
Candidates screened before survodutide was picked

The short answer

What is the difference between retatrutide, mazdutide and survodutide?

The number of hormone receptors each one switches on. Retatrutide works on three: the receptors for GLP-1, GIP and glucagon [1]. Mazdutide and survodutide work on two: GLP-1 and glucagon [4] [2].

An agonist is a molecule that switches a receptor on. That is why you see retatrutide called a triple agonist and the other two called dual agonists. The labels count receptors. They do not rank the compounds.

So the gap is GIP. GLP-1 and GIP are hormones the gut releases after a meal. Glucagon is made in the pancreas and acts mainly on the liver. Mazdutide and survodutide leave the GIP receptor out. Retatrutide adds it.

All three are synthetic peptides, linked to different companies in the papers. Retatrutide comes from Eli Lilly [1]. Survodutide comes from Boehringer Ingelheim [2]. Mazdutide carries a Lilly code and an Innovent Biologics code, and its trials were run in China [4].

A tray of capped vials

The three side by side

RetatrutideMazdutideSurvodutide
ReceptorsGLP-1, GIP and glucagonGLP-1 and glucagonGLP-1 and glucagon
Called aTriple agonistDual agonistDual agonist
Codes in papersLY3437943IBI362, LY3305677BI 456906
Company in the papersEli LillyInnovent BiologicsBoehringer Ingelheim
First paper here2022, Cell Metabolism2021, EClinicalMedicine2022, Molecular Metabolism

Retatrutide

Where does retatrutide come from?

Eli Lilly scientists described retatrutide in 2022 under the code LY3437943. They tested it in cells carrying each receptor, then in mice, then in a first small study in people [1].

Other labs have used it since. A German team took heart tissue from mice, kept it beating in an organ bath, and measured whether retatrutide changed how it beat [7]. A Japanese research company put it in the same mouse study as semaglutide and tirzepatide [8].

Retatrutide is the only one of the three in our catalog. It comes as a white freeze-dried powder, kept frozen and away from light until it is reconstituted for lab work.

For how it lines up against its two-receptor cousin from the same company, see retatrutide vs tirzepatide. The plain-English background is in the retatrutide guide.

A person reading a certificate of analysis

Survodutide

Where does survodutide come from?

Boehringer Ingelheim scientists described it in 2022 under the code BI 456906. Their rationale drew on oxyntomodulin, a gut peptide that switches on both the glucagon and GLP-1 receptors. They tested the new peptide in cell assays and then in animal studies [2].

A 2024 paper from the same company explained how it was chosen. The team started with 19 candidate dual agonists and narrowed them down with lab tests: hamster cells built to carry the human receptors, mouse cells, and rat liver cells [3].

Both of those papers are lab and animal work. For a research comparison, that makes them a good place to start: the cell tests show which receptors the peptide engages before any study in people [2] [3].

Oxyntomodulin is worth knowing because it shows the idea. The body already makes a peptide that switches on the glucagon and GLP-1 receptors together. Survodutide follows that two-receptor pattern, and mazdutide works on the same pair. Retatrutide goes one step further and adds GIP.

A tray of vials in an HPLC instrument
  1. 01

    Start with 19 candidates

    Peptides built to switch on both the glucagon and GLP-1 receptors.

  2. 02

    Test in cells

    Hamster cells carrying the human receptors, plus mouse and rat cells.

  3. 03

    Test in animals

    Check that each receptor is engaged in a living animal.

  4. 04

    Pick one

    Three went to deeper profiling. BI 456906 went forward and was later named survodutide.

Mazdutide

Where does mazdutide come from?

Mazdutide shows up in papers under two codes, IBI362 and LY3305677. The papers call it a GLP-1 and glucagon dual agonist [4].

The early papers print both codes side by side. Later papers use the name mazdutide, with IBI362 next to it [6]. If you are reading older work, search for the codes as well as the name, or you will miss papers.

The early papers on it are trials in people, run in China with Innovent Biologics [4] [5] [6]. We sell research material, so this page does not cover what those trials found.

Two laboratory benches with instruments

The family

Why do these three get compared?

They belong to the same family of lab-made peptides built on gut hormones. Each one is designed to switch on more than one receptor at a time. A 2025 review in the journal Peptides covers the whole family, from one-receptor compounds to the newer multi-receptor ones [9].

The useful way to sort them is by receptor count. Two receptors for mazdutide and survodutide, three for retatrutide. When a paper names more than one of them, check which result goes with which compound.

Papers also test a multi-receptor peptide next to other gut-hormone peptides in the same animals. One example put retatrutide next to semaglutide and tirzepatide in the same mouse study [8]. Side-by-side work like that shows how compounds with different receptor counts compare under the same conditions.

Close-up of a vial cap

Two receptors or three

Two receptors
  • Mazdutide
  • Survodutide
  • GLP-1 and glucagon
  • No GIP
Three receptors
  • Retatrutide
  • GLP-1, GIP and glucagon
  • Adds GIP to the pair

In our catalog

Which of these does SBz carry?

We stock retatrutide in 10, 30 and 60 mg vials, sold for laboratory research only. We do not carry mazdutide or survodutide. Our GLP-1 category lists every related compound we do stock, and each product page posts its lab certificate as results come in.

If you are planning a comparison study, write down the codes and the receptor counts at the start, so your notes match the papers you cite.

Reading a paper on any of the three
  • Check which compound each result belongs to
  • Check how many receptors it works on
  • Check what it was tested in: cells, animal tissue, mice or people
  • Match the code in the paper to the name

Questions

Common questions

Is mazdutide the same as retatrutide?

No. Mazdutide works on two receptors, GLP-1 and glucagon. Retatrutide works on three, adding GIP.

Is survodutide the same as mazdutide?

No. They are different peptides, linked to different companies in the papers. Both work on the GLP-1 and glucagon receptors.

What do the codes mean?

Drug makers name a compound with a code before it gets a name. LY is Eli Lilly, BI is Boehringer Ingelheim and IBI is Innovent Biologics.

Do you sell mazdutide or survodutide?

No. We stock retatrutide, for laboratory research only.

Sources

Every study mentioned on this page

Each one links to its record on PubMed, the US National Library of Medicine database.

  1. LY3437943, a novel triple glucagon, GIP, and GLP-1 receptor agonist for glycemic control and weight loss: From discovery to clinical proof of conceptCoskun and colleagues, Eli Lilly and Company. Cell Metabolism, 2022. The retatrutide discovery paper: receptor tests in cells, then mice, then a first small study in people.
  2. BI 456906: Discovery and preclinical pharmacology of a novel GCGR/GLP-1R dual agonist with robust anti-obesity efficacyZimmermann and colleagues, Boehringer Ingelheim. Molecular Metabolism, 2022. The survodutide discovery paper: cell assays, then animal studies.
  3. The dual GCGR/GLP-1R agonist survodutide: Biomarkers and pharmacological profiling for clinical candidate selectionThomas and colleagues, Boehringer Ingelheim. Diabetes, Obesity and Metabolism, 2024. How survodutide was picked from 19 candidates, using hamster, mouse and rat cells and animal tests.
  4. IBI362 (LY3305677), a weekly-dose GLP-1 and glucagon receptor dual agonist, in Chinese adults with overweight or obesity: A randomised, placebo-controlled, multiple ascending dose phase 1b studyJi and colleagues, Peking University People's Hospital and Innovent Biologics. EClinicalMedicine, 2021. An early trial in people in China, under the codes IBI362 and LY3305677.
  5. A phase 1b randomised controlled trial of a glucagon-like peptide-1 and glucagon receptor dual agonist IBI362 (LY3305677) in Chinese patients with type 2 diabetesJiang and colleagues, hospitals in China and Innovent Biologics. Nature Communications, 2022. A second early trial in people in China.
  6. Safety and efficacy of a GLP-1 and glucagon receptor dual agonist mazdutide (IBI362) 9 mg and 10 mg in Chinese adults with overweight or obesity: A randomised, placebo-controlled, multiple ascending dose phase 1b trialJi and colleagues, China. EClinicalMedicine, 2022. A trial paper that uses the name mazdutide next to the code IBI362.
  7. Contractile effects of retatrutide in isolated mouse atrial preparationsNeumann and colleagues, Martin Luther University Halle-Wittenberg. Naunyn-Schmiedeberg's Archives of Pharmacology, 2025. Heart tissue taken from mice and kept beating in an organ bath.
  8. Efficacy of GLP-1 analog peptides, semaglutide, tirzepatide, and retatrutide on MC4R deficient obesity and their comparisonHitaka and colleagues, Axcelead Drug Discovery Partners. International Journal of Obesity, 2026. Mice bred without the MC4R gene, given one of three compounds in the same study.
  9. Multifunctional incretin peptides in therapies for type 2 diabetes, obesity and associated co-morbiditiesBailey and colleagues, Aston University and Ulster University. Peptides, 2025. A review of the gut-hormone peptide family, from one-receptor to multi-receptor compounds.

For the lab

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Every product is sold for laboratory research use only. Posted lab reports, with their report numbers, are on the product page.

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