PROGRAMME · METABOLIC
Incretin Biology
Research programme covering the incretin axis: GLP-1, GIP and glucagon receptor pharmacology, mono / dual / triple agonist chemistry, and the landmark clinical evidence base.
3 compounds3 mechanisms17 studies34 glossary terms
Included compounds
- RetatrutideLY3437943
- SemaglutideNN9535 · Ozempic (brand) · Wegovy (brand) · Rybelsus (brand — oral)
- TirzepatideLY3298176 · Mounjaro (brand) · Zepbound (brand — obesity)
Core mechanisms
- GLP-1 ReceptorGlucagon-like peptide-1 receptor ligands.
- GIP ReceptorGlucose-dependent insulinotropic polypeptide receptor ligands.
- Glucagon ReceptorGlucagon receptor ligands.
Landmark literature
- SUSTAIN-62016 · New England Journal of Medicine
- STEP2021 · New England Journal of Medicine (STEP-1 lead publication)
- SELECT2023 · New England Journal of Medicine
- FLOW2024 · New England Journal of Medicine
- STEP-12021 · New England Journal of Medicine
- STEP-22021 · Lancet
- STEP-32021 · JAMA
- STEP-42021 · JAMA
- STEP-52022 · Nature Medicine
- STEP-82022 · JAMA
- SURPASS-12021 · Lancet
- SURPASS-22021 · New England Journal of Medicine
- SURPASS-32021 · Lancet
- SURPASS-42021 · Lancet
- SURPASS-52022 · JAMA
- Retatrutide Phase 2 (Obesity)2023 · New England Journal of Medicine
- Retatrutide Phase 2 (Diabetes)2023 · Lancet
Comparisons
Research guides
- What is Retatrutide?Introductory reference on Retatrutide (LY3437943) — a triple-agonist investigational peptide referenced in incretin pharmacology literature.
- Retatrutide Mechanism of ActionReceptor-level explanation of Retatrutide's activity at GLP-1R, GIPR and GCGR as reported in the published preclinical and clinical literature.
- GLP-1 Receptor ExplainedOverview of the GLP-1 receptor: a Class B G-protein-coupled receptor central to incretin pharmacology and to a growing family of research peptides.
- GIP Receptor ExplainedOverview of the GIP receptor: a class B G-protein-coupled receptor engaged by dual and triple incretin-agonist research peptides.
- Glucagon Receptor ExplainedOverview of the glucagon receptor (GCGR): classification, hepatic signalling and its role as the third receptor in triple-agonist research peptides.
- Triple Agonists ExplainedEducational overview of triple GLP-1 / GIP / glucagon receptor agonists — pharmacological rationale, structural strategy and comparison to single- and dual-agonist analogues.
- Retatrutide Research ApplicationsEducational review of in-vitro and translational research applications for Retatrutide (LY3437943) as a reference standard.
- Retatrutide FAQComprehensive frequently asked questions about Retatrutide (LY3437943): identity, pharmacology, storage, applications and regulatory status.
- What is Semaglutide?Beginner-friendly research-focused introduction to Semaglutide — a long-acting GLP-1 receptor agonist derived from native GLP-1(7-37).
- Semaglutide Mechanism of ActionReceptor-level explanation of Semaglutide's activity at GLP-1R — Gαs / cAMP / PKA / EPAC2 signalling, β-arrestin recruitment, insulinotropic and glucagonostatic effects, gastric emptying and central appetite modulation.
- Semaglutide FAQComprehensive research-focused FAQ on Semaglutide — identity, receptor pharmacology, structural modifications, pharmacokinetics, laboratory handling, evidence base and regulatory status.
- Semaglutide PharmacokineticsReported pharmacokinetics of Semaglutide — half-life, albumin binding, C18 di-acid acylation, absorption for subcutaneous vs oral formulations, distribution, steady state and research limitations.
- Semaglutide Research ApplicationsOverview of published Semaglutide research contexts — metabolic, cardiovascular, renal, neuroinflammation/CNS and NAFLD/MASH — with a clear preclinical vs human evidence split.
- Albumin Binding and Half-Life ExtensionReusable mechanism guide explaining how fatty-acid acylation supports reversible non-covalent binding to serum albumin, and how that extends the plasma half-life of GLP-1 peptides.
- Incretin Effect ExplainedFoundation guide to the incretin effect — how GLP-1 and GIP amplify glucose-dependent insulin secretion, the physiology of gut L- and K-cells, and how incretin biology underpins GLP-1 receptor agonist research.
- What is Tirzepatide?Beginner-friendly research-focused introduction to Tirzepatide — a dual GIP / GLP-1 receptor agonist positioned between Semaglutide and Retatrutide in incretin pharmacology.
- Tirzepatide Mechanism of ActionReceptor-level explanation of Tirzepatide as a dual GIP / GLP-1 receptor agonist — dual cAMP / PKA signalling, biased β-arrestin engagement at GLP-1R, GIP-adipocyte biology and integrated satiety signalling.
- Tirzepatide FAQComprehensive research-focused FAQ on Tirzepatide — identity, dual-receptor pharmacology, structural modifications, pharmacokinetics, laboratory handling, evidence base and regulatory status.
Methodology
No entries yet.
Glossary
- GLP-1
- Incretin
- Incretin Effect
- GLP-1 Receptor Agonist
- Biased Agonism
- Beta-Arrestin
- cAMP / PKA Signalling
- EPAC2
- Gastric Emptying
- POMC Neuron
- NPY Neuron
- Insulinotropic
- Glucagonostatic
- Acylation
- Albumin Binding
- SNAC
- Subcutaneous Administration
- Steady State
- Receptor Internalisation
- Desensitisation
- MACE
- DIO Model
- Native GLP-1
- Oral Semaglutide
- Semaglutide
- Dual Incretin Agonism
- GIP-Adipocyte Axis
- Satiety Signalling
- Gs Protein
- C20 Fatty Diacid
- Weekly Dosing Pharmacokinetics
- SURPASS Programme
- SURMOUNT Programme
- HbA1c Endpoint
Related research areas
- Peptide Chemistry
- Receptor Studies
Reading pathways
Programme metadata governed by the Research Hub framework.
