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For laboratory research use only. Not for human or veterinary use.
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Synthetic peptide, incretin-receptor agonist
Also catalogued as LY3298176, LY-3298176.
An engineered 39-residue sequence containing two aminoisobutyric-acid residues and a C20 fatty-diacid attachment at position 20; a plain one-letter rendering would misstate it.
Tirzepatide (developed under the code LY3298176) is a synthetic peptide of thirty-nine residues based on the sequence of glucose-dependent insulinotropic polypeptide (GIP). The design incorporates two aminoisobutyric-acid residues and a C20 fatty-diacid moiety attached through a linker to the lysine at position 20.
In the primary literature it is characterised pharmacologically as a dual agonist of the GIP and GLP-1 receptors. Its discovery and characterisation were published by Coskun and colleagues in 2018.
Tirzepatide is the active ingredient of prescription products approved by the U.S. FDA, first in May 2022 (Mounjaro). The research material listed here is not those products and is not a drug.
Coskun T, Sloop KW, Loghin C, et al. LY3298176, a novel dual GIP and GLP-1 receptor agonist for the treatment of type 2 diabetes mellitus: From discovery to clinical proof of concept. Molecular Metabolism 2018;18:3–14.
Citation titles are reproduced verbatim from the journal record. A citation documents the molecule's published identity and history; it is not a claim about the material sold here.