Peptide Handbook
Metabolic Peptides

Liraglutide

Selective GLP-1 Receptor Agonist

Updated April 14, 2026

What is Liraglutide?

A 31-amino-acid acylated GLP-1 analog with 97% homology to native human GLP-1(7-37), modified with a C16 palmitoyl fatty acid chain enabling albumin binding and extending its half-life from 2 minutes to approximately 13 hours. The SCALE Obesity and Prediabetes trial demonstrated 8.0% mean weight reduction at 56 weeks with the 3.0 mg dose. As a once-daily injectable, liraglutide bridges the pharmacokinetic gap between short-acting exenatide and weekly semaglutide.

Research Profile

Structure 31 amino acids, C₁₇₂H₂₆₅N₄₃O₅₁
Targets GLP-1R (selective, high affinity)
Research Focus Incretin pharmacokinetics, β-cell preservation, daily vs weekly GLP-1 dosing, appetite regulation
Reconstitution Bacteriostatic water — 1 mg/mL
Stability 28 days at 2–8°C
Key distinction: Once-daily GLP-1 agonist with the longest clinical track record of any incretin — FDA-approved since 2010. The C16 palmitoyl chain enables albumin-mediated half-life extension without PEGylation.

Published Research

[1] Pi-Sunyer X et al. A Randomized, Controlled Trial of 3.0 mg of Liraglutide in Weight Management (SCALE). NEJM 2015;373:11-22 — PubMed 26132939
[2] Knudsen LB et al. The discovery and development of liraglutide and semaglutide. Front Endocrinol 2019;10:155 — PubMed 31031702
Research Use Only. All products sold by Lumen Peppers are intended solely for in vitro research and laboratory purposes. They are not drugs, supplements, or foods. Nothing on this page constitutes medical advice. Researchers are responsible for compliance with all applicable regulations. Last updated: April 14, 2026.

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