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10 mg
CAS#
2381089-83-2
Formula
C221H343N51O64
M.W.
4,731.40 g/mol
PURITY99% HPLC
RUONot for human or veterinary use
Retatrutida 10 mg — MX-1 Labs
10 mg

Retatrutida

Triple GIP/GLP-1/Glucagon agonist · Metabolism

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MX$2,070.00
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2+MX$1,967.005%
3+MX$1,863.0010%
5+MX$1,760.0015%
10+MX$1,656.0020%

Retatrutida 10 mg (LY3437943) is a lyophilized research compound — a synthetic 39-modified-amino-acid peptide with identity confirmed by mass spectrometry and ≥99% purity verified by HPLC. Every batch ships with a traceable CoA.

Verified by HPLC
Lot
RETA-2026-A01
Purity
99.2%
Expires
2027-03

Technical specifications

Download CoA (PDF)
Active batchRETA-2026-A01View this batch CoA (PDF)
Molecular weight
~4,731 Da
Sequence
Synthetic peptide of 39 modified amino acids
Format
Sterile lyophilized
Content
10 mg per vial
Purity
≥99% verified by HPLC in batch CoA
Identity
Confirmed by mass spectrometry (MS)
Storage
Batch traceability and thermal chain documentation
Endotoxins (LAL)
< 5 EU/mg
Water content (Karl Fischer)
< 6%
Amino acid analysis
Composition confirmed by acid hydrolysis

About Retatrutida 10 mg

Retatrutida (LY3437943) is a synthetic 39-amino-acid peptide designed as a triple agonist at the GIP (glucose-dependent insulinotropic polypeptide), GLP-1 (glucagon-like peptide-1), and Glucagon receptors. Identity and purity are verified by mass spectrometry and reverse-phase HPLC, with individual results reported in the Certificate of Analysis (CoA) for each batch.

Initial characterization of the compound was published by Coskun and colleagues in Cell Metabolism (2022) [1], and preclinical data from the research program are registered in peer-reviewed scientific literature and the public trials registry [2].

MX-1 Labs distributes Retatrutida 10 mg in Mexico as a scientific research compound with laboratory packaging, an auditable batch number, and complete per-vial analytical documentation. The product is intended exclusively for in vitro laboratory research; it is not a medication, supplement, or consumer product.

Research applications

Retatrutida acts simultaneously on three well-characterized G protein-coupled receptors in endocrinological literature: GIP, GLP-1, and the Glucagon receptor [1]. In preclinical models, combined activation of the first two is associated with effects on satiety, insulin sensitivity, and energy expenditure, while the glucagon component distinguishes Retatrutida from classical dual agonists by engaging hepatic lipolysis as an additional mechanism. The peptide structure includes non-canonical amino acid modifications and conjugation with a fatty acid to extend the plasma half-life observed in pharmacokinetic studies. The specific experimental application is the responsibility of the receiving lab and its authorized institutional SOP.

Storage and handling

Sealed vial: store protected from light, humidity, and prolonged air exposure per the batch documentation. Once the experimental solution is prepared, keep refrigerated under documented conditions when the lab protocol requires it; record the preparation date, diluent used, and workstation conditions. Stability of the prepared solution depends on the batch-specific CoA, the diluent, aseptic technique, and the research protocol. Discard the material at any sign of turbidity, suspended particles, or any color change from the initial observation.

Scientific references

  1. Coskun T et al. LY3437943, a novel triple GIP/GLP-1/glucagon receptor agonist. Cell Metabolism 2022; 34(9):1234–1247. View source on PubMed →
  2. ClinicalTrials.gov — Registered studies for the clinical development of retatrutida. View registry →

Frequently asked questions

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