Influence of Selective Fluorination on the Biological Activity and Proteolytic Stability of Glucagon-like Peptide-1
Journal of Medicinal Chemistry2008Vol. 51(22), pp. 7303–7307
Citations Over TimeTop 21% of 2008 papers
Abstract
The relative simplicity and high specificity of peptide therapeutics has fueled recent interest. However, peptide and protein drugs generally require injection and suffer from low metabolic stability. We report here the design, synthesis, and characterization of fluorinated analogues of the gut hormone peptide, GLP-1. Overall, fluorinated GLP-1 analogues displayed higher proteolytic stability with simultaneous retention of biological activity (efficacy). Fluorinated amino acids are useful for engineering peptide drug candidates and probing ligand-receptor interactions.
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