Improving on Nature: Making a Cyclic Heptapeptide Orally Bioavailable1. (12th September 2014)

• Record Type: Journal Article
• Authors: Nielsen, Daniel S.; Hoang, Huy N.; Lohman, Rink‐Jan; Hill, Timothy A.; Lucke, Andrew J.; Craik, David J.; Edmonds, David J.; Griffith, David A.; Rotter, Charles J.; Ruggeri, Roger B.; Price, David A.; Liras, Spiros; Fairlie, David P.
• Is Part Of: Angewandte Chemie. Volume 126:Number 45(2014)
• Page Start: 12255
• Page End: 12259
• Publication Date: 2014-09-12
• Subjects: Chemistry -- Periodicals; 540
• DOI: 10.1002/ange.201405364
• Languages: English
• ISSNs: 0044-8249

Abstract

<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>The use of peptides in medicine is limited by low membrane permeability, metabolic instability, high clearance, and negligible oral bioavailability. The prediction of oral bioavailability of drugs relies on physicochemical properties that favor passive permeability and oxidative metabolic stability, but these may not be useful for peptides. Here we investigate effects of heterocyclic constraints, intramolecular hydrogen bonds, and side chains on the oral bioavailability of cyclic heptapeptides. NMR‐derived structures, amide H–D exchange rates, and temperature‐dependent chemical shifts showed that the combination of rigidification, stronger hydrogen bonds, and solvent shielding by branched side chains enhances the oral bioavailability of cyclic heptapeptides in rats without the need for N‐methylation.</p> </abstract>