PeptidePedia The community reference

Orforglipron (revision 5)

Old revision·05:46, 2 Jan 2025·DPP4_Dagmar

This is an old revision of this page, as it stood at 05:46, 2 Jan 2025, saved by DPP4_Dagmar with the summary expand §Reported clinical findings. It may differ substantially from the current revision, and any error it contains may since have been corrected.
Orforglipron
Development codeLY3502970
ClassSmall-molecule GLP-1 receptor agonist
RouteOral, once daily
StatusPhase 3; not approved
Compound infobox · conventions

Orforglipron (development code LY3502970) is an investigational orally administered non-peptide agonist of the GLP-1 receptor. It is not a peptide and is not subject to proteolysis, so it requires neither an absorption enhancer nor the strict fasting conditions that govern oral semaglutide.[1]

Small-molecule agonism at a class B G-protein-coupled receptor was long considered difficult, because the natural ligand engages a large surface across two receptor domains.[2] Orforglipron binds a pocket near the extracellular face of the transmembrane bundle and stabilises an active conformation without reproducing the peptide's binding mode.[1]

Reported phase 2 results include glycated-haemoglobin reductions of up to about 2.1 percentage points in type 2 diabetes and weight reduction of up to about 14.7% at 36 weeks in obesity without diabetes. It is not approved in any jurisdiction.[3]

Molecular basis

[edit]

The receptor's orthosteric peptide site is a poor target for a small molecule: the natural ligand contacts both the extracellular domain and the transmembrane bundle across a large interface, and a molecule of a few hundred daltons cannot reproduce that. Orforglipron instead occupies a pocket accessible from the extracellular face of the bundle and acts as an agonist by stabilising the same active receptor conformation by a different route.[1]

A consequence is species selectivity. The pocket differs between human and rodent receptors sufficiently that activity does not translate, and preclinical work required humanised receptor models — a practical complication of small-molecule work at this target that peptide agonists do not face.

References

  1. ^ a b c Kawai T, Sun B, Yoshino H, et al. "Structural basis for GLP-1 receptor activation by LY3502970, an orally active nonpeptide agonist." Proceedings of the National Academy of Sciences 117(47):29959–29967 (2020). DOI:10.1073/pnas.2014879117. PMID 33177239.
  2. ^ de Graaf C, Donnelly D, Wootten D, et al. "Glucagon-like peptide-1 and its class B G protein-coupled receptors." Pharmacological Reviews 68(4):954–1013 (2016). PMID 27630114.
  3. ^ Frías JP, Hsia S, Eyde S, et al. "Efficacy and safety of oral orforglipron in patients with type 2 diabetes: a phase 2 randomised trial." The Lancet 402(10400):472–483 (2023). PMID 37369232.