Page data last changed: . Registry refreshes and identity assessments are separate from scientific content review.
Venom-derived GLP-1 mimetic resistant to DPP-4.
Part of the Metabolic & GLP-1 peptides cluster
Overview
Exendin-4 is a 39-residue peptide from Gila monster venom that activates the GLP-1 receptor and inspired the drug exenatide.
Source & context
Biological / chemical source: Gila monster venom homolog
Primary research or clinical context: Basis for exenatide (approved)
From venom to medicine
Exendin-4’s resistance to DPP-4 cleavage made it a template for incretin mimetic drugs — a famous natural-product-to-pharmacy story in peptide science.
Sequence of the selected reference form
Sequence backbone for the reference form: Exendin-4 parent peptide amide. Termini, stereochemistry and modifications are described below.
HGEGTFTSDLSKQMEEEAVRLFIEWLKNGGPSSGAPPPS
Analyze sequences in the playground →Structure & chemistry
Molecular identity & reference confidence
Source-supported reference
The selected reference is the 39-residue Heloderma suspectum exendin-4 peptide amide, identical in sequence to exenatide. The imported CIDs omit all or some stereochemistry; CID 45588096 supplies the complete stereoisomer.
- Molecular form
- Exendin-4 parent peptide amide
- Species
- Heloderma suspectum (natural sequence); selected molecular reference is not a claim of venom extraction
- Termini (N / C)
- Free histidyl amino terminus / L-serinamide (Ser39-NH2)
Average reference mass · Molecular identity assessment: 2026-10-05
Reference policy updated: 2026-10-05
- PubChem PUG REST selected parent properties · 2026-10-05
- PubChem selected-parent biologic notation · 2026-10-05
- PubChem selected-parent identifiers with depositor attribution · 2026-10-05
- NIH GSRS independently selected parent record · 2026-10-05
- Official product label chemical description, selected parent distinguished from formulation · 2026-10-05
- Eng et al., original isolation/characterization of exendin-4 (1992) · 2026-10-05
H-His-Gly-Glu-Gly-Thr-Phe-Thr-Ser-Asp-Leu-Ser-Lys-Gln-Met-Glu-Glu-Glu-Ala-Val-Arg-Leu-Phe-Ile-Glu-Trp-Leu-Lys-Asn-Gly-Gly-Pro-Ser-Ser-Gly-Ala-Pro-Pro-Pro-Ser-NH2
- Molecular formula
- C184H282N50O60S
- Average reference mass
- ≈ 4,186.6
- Backbone
- Exendin-4 parent peptide amide
- C-terminus
- L-serinamide (Ser39-NH2)
- PubChem CID: 45588096
- CAS RN: 141758-74-9
- UNII: 9P1872D4OL
Chemistry values: curated profile, PubChem.
Clinical development snapshot
ClinicalTrials.gov lists 378 registered studies with “Exendin-4” as an intervention (snapshot 2026-10-01). A registry footprint is not evidence of efficacy or approval.
| NCT | Title | Phase | Status | Updated |
|---|---|---|---|---|
| NCT05663515 | A Pan-European Post-Authorisation Safety Study: Risk of Pancreatic Cancer Among Type 2 Diabetes Patients Who I | — | recruiting | 2026-09-24 |
| NCT01988545 | GLP-1's Effect on Cardiac Parameters and Mesenteric Blood Flow | Not applicable | completed | 2026-09-15 |
| NCT07808879 | Comparison of [68Ga]Ga-HBED-CC-PEG6-Exendin-4 and [68Ga]Ga-HBED-CC-Exendin-4 PET/CT for Insulinoma Localizatio | Not applicable | recruiting | 2026-09-09 |
| NCT06725693 | Glucagon-like Peptide-1 Receptor PET/CT in GLP-1R Related Disease | — | recruiting | 2026-09-08 |
| NCT05220917 | Comparative Effectiveness and Safety of Four Second Line Pharmacological Strategies in Type 2 Diabetes Study | — | active not recruiting | 2026-08-13 |
| NCT07702461 | Determination of Resistance Training Status for Patients on Glucagon-Like Peptide-1 Receptor Agonists | — | recruiting | 2026-07-24 |
Exendin-4 — reconstitution calculator
Enter how much peptide is in the vial and how much diluent (e.g. bacteriostatic water) is added. The tool returns the resulting solution concentration — and, for any amount you type, the volume it corresponds to. This is educational arithmetic, not a dosing recommendation.
Reference form: Exendin-4 parent peptide amideAverage reference mass: 4,186.6 Da
Enter an amount to see the volume it corresponds to.
Educational concentration mathematics only. This tool does not recommend a dose, amount, or protocol, and nothing here is medical advice. Many peptides are not authorized by Health Canada for human use — see our reconstitution and bacteriostatic-water guides for context.
Change log
Dated observations from the data pipeline (registry flags, trial footprints, identifiers) and editorial reviews of this profile.
- Trials1 registered study added on ClinicalTrials.gov (now 378).
FAQ about Exendin-4
What is Exendin-4?+
Exendin-4 is a 39-residue peptide from Gila monster venom that activates the GLP-1 receptor and inspired the drug exenatide.
What Canadian product status is recorded for Exendin-4?+
Canadian product status for Exendin-4 has not been verified in this profile. No verified record here does not mean no authorization exists. Status depends on the product, formulation and use; consult Health Canada's product records.
What is the length of the selected reference form for Exendin-4?+
The selected reference form (Exendin-4 parent peptide amide) has 39 residues or residue-derived units in its backbone. Other forms in this family may have a different length.
Related peptides
References & further reading
- 1.Eng et al. (1992). Isolation and characterization of exendin-4, an exendin-3 analogue, from Heloderma suspectum venom. Further evidence for an exendin receptor on dispersed acini from guinea pig pancreas. J Biol Chem
- 2.Esparza-Salazar et al. (2021). Exendin-4 for Parkinson's disease. Brain Circ
- 3.Jansen et al. (2019). Exendin-4 analogs in insulinoma theranostics. J Labelled Comp Radiopharm
- 4.Wang et al. (2025). Exendin-4 Prevents oxLDL-Induced upregulation of TREM2 and attenuates foam cell formation and inflammation in Macrophages. Biochem Pharmacol
- 5.Khine et al. (2025). Exendin-4 improves mitochondrial integrity against cisplatin-induced cardiac damage: Targeting p53 and NF-κB pathways. Eur J Pharmacol
- 6.Verma et al. (2024). Exendin-4: A potential therapeutic strategy for Alzheimer's disease and Parkinson's disease. Chem Biol Drug Des
- 7.Ahn et al. (2021). Exendin-4 Pretreatment Attenuates Kainic Acid-Induced Hippocampal Neuronal Death. Cells
- 8.Rajabi et al. (2022). Exendin-4 as a Versatile Therapeutic Agent for the Amelioration of Diabetic Changes. Adv Pharm Bull
- 9.PubChem — compound summary for Exenatide (CID 45588096)
- 10.Wikipedia — Exenatide (synthetic exendin-4)