Journal article

Improving oral bioavailability of peptides by multiple N-methylation: Somatostatin analogues

E Biron, J Chatterjee, O Ovadia, D Langenegger, J Brueggen, D Hoyer, HA Schmid, R Jelinek, C Gilon, A Hoffman, H Kessler

Angewandte Chemie International Edition | Published : 2008

Abstract

Full methyl jacket? A complete library of the N-methylated somatostatin cyclopeptidic analogue Veber-Hirschmann peptide cyclo(-PFwKTF-) has been prepared with the aim of improving its bioavailability. Several analogues from the library were found to bind to the somatostatin receptor in the nanomolar range and one of them shows a significant oral bioavailability of 10%. Conformational analysis shows that N-methylationis allowed at specific positions without affecting the bioactive conformation. (Figure Presented) © 2008 Wiley-VCH Verlag GmbH & Co. KGaA.

University of Melbourne Researchers