Tirzepatide (LY3298176) is a synthetic 39-amino-acid linear peptide engineered as a single-molecule dual agonist of the glucose-dependent insulinotropic polypeptide receptor (GIPR) and the glucagon-like peptide-1 receptor (GLP-1R). Its sequence is derived from the native GIP backbone and incorporates two 2-aminoisobutyric acid (Aib) substitutions, a C-terminal amide, and a C20 fatty-diacid moiety attached to the Lys20 side chain through a γ-glutamate / di-AEEA linker. It is offered strictly as a characterized reference material for in-vitro and analytical research. For Research Use Only — not for human or veterinary use.
Molecular identity
A 39-residue linear peptide with the molecular formula C₂₂₅H₃₄₈N₄₈O₆₈ and a monoisotopic/average molecular weight of approximately 4813.5 g/mol (CAS 2023788-19-2; PubChem CID 156588324). The sequence carries 2-aminoisobutyric acid (Aib) at positions 2 and 13 and a C-terminal amide.
Structural features
The Lys20 side chain is conjugated to a 1,20-eicosanedioic (C20) fatty diacid through a glutamic-acid spacer and two (2-(2-aminoethoxy)ethoxy)acetic acid (AEEA) units. This lipidation is discussed in the literature as the basis for albumin association, while the Aib substitutions are associated with resistance to dipeptidyl-peptidase cleavage in characterization studies.
Research context
In published in-vitro work, Tirzepatide is examined as a tool for probing simultaneous engagement of two incretin receptors (GIPR and GLP-1R) and the associated G-protein-coupled signaling, including comparative cAMP-response and receptor-binding assays relative to native incretins and single-target agonists.
Handling as a reference material
Supplied as a lyophilized powder at ≥98% (HPLC) purity for laboratory analytical and receptor-assay applications. Identity and purity are appropriate for use as an analytical reference standard. For Research Use Only; not intended for any in-vivo, diagnostic, or therapeutic application.
Every Tirzepatide order includes a sealed, lot-controlled vial, the completed lot documentation, and a handling & storage card. Product-specific handling follows the supplied documentation and institutional SOPs.
Evidence limits and research safety
Research findings can differ by model, assay, purity, formulation, and study design. Published cell, biochemical, and pre-clinical observations do not establish human or veterinary safety, efficacy, dosing, or suitability. Researchers should review the applicable SDS, institutional safety procedures, waste requirements, and lot-specific documentation before handling any reference material.
Related research
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Credible sources
- PubChem CID 156588324 — Tirzepatide
- PubChem search — Tirzepatide
- PubMed — Tirzepatide GIP/GLP-1 literature