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MONOGRAPH No. 123
TYPE
GLP-1 agonist
MW
4186.6 g/mol
CAS
141732-76-5
EU STATUS
EMA approved (Byetta/Bydureon)
WADA
Not prohibited
MIN PURITY
≥98% HPLC
⚖ GLP-1 & Weight

Exenatide — EU research guide.

Exenatide is the original GLP-1 receptor agonist, derived from a peptide found in Gila monster venom — the foundation compound that opened the entire incretin drug class now led by semaglutide and tirzepatide.

Last reviewed:

What is Exenatide?

Exenatide is a synthetic version of exendin-4, a GLP-1-receptor-activating peptide first isolated from Gila monster saliva. It slows gastric emptying, boosts glucose-dependent insulin release and reduces appetite, administered as Byetta (twice-daily) or Bydureon (once-weekly extended-release).

What does the research show?

Approved by the FDA in 2005 and the EMA shortly after, exenatide has decades of outcomes data in type 2 diabetes, including the EXSCEL cardiovascular-safety trial. Its weight-loss effect is modest compared with newer analogues, which is why it has been largely superseded by liraglutide, semaglutide and tirzepatide.

EU legal status

EMA-approved prescription medicine for type 2 diabetes; also available as a research-grade peptide from RUO suppliers.

⚠ Superseded by longer-acting, more effective GLP-1 analogues for most indications; still prescribed in some diabetes protocols.
✓ For the current-generation GLP-1 compounds, PeptideCompare tracks semaglutide and tirzepatide from EU research vendors with COA documentation.

Molecular information

Molecular formula
C184H282N50O60S
Molecular weight
4186.6 g/mol
CAS number
141732-76-5

Pharmacokinetics

Half-life (t½)
≈ 2.4 h
Tmax
≈ 2.1 h
Source: FDA Byetta label

GLP-1 compounds across EU suppliers

COA-verified EU vendors · Updated monthly

Frequently asked questions

What is Exenatide? ▾

Exenatide is a synthetic version of exendin-4, a GLP-1-receptor-activating peptide first isolated from Gila monster saliva. It slows gastric emptying, boosts glucose-dependent insulin release and reduces appetite.

What does the research show? ▾

Approved by the FDA in 2005 and the EMA shortly after, it has decades of type 2 diabetes outcomes data including the EXSCEL cardiovascular-safety trial, though its weight-loss effect is modest compared with newer analogs.

Why has exenatide been largely superseded? ▾

Its weight-loss effect is modest compared with newer analogs, which is why it has been largely replaced by liraglutide, semaglutide and tirzepatide.

What is the difference between Byetta and Bydureon? ▾

Byetta is the twice-daily form and Bydureon is the once-weekly extended-release form of exenatide.

Is exenatide legal in the EU? ▾

It is an EMA-approved prescription medicine for type 2 diabetes and is also available as a research-grade peptide.

Is exenatide banned in sport? ▾

No. It is not prohibited by WADA.

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