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

311Citations
Citations of this article
232Readers
Mendeley users who have this article in their library.
Get full text

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.

Cite

CITATION STYLE

APA

Biron, E., Chatterjee, J., Ovadia, O., Langenegger, D., Brueggen, J., Hoyer, D., … Kessler, H. (2008). Improving oral bioavailability of peptides by multiple N-methylation: Somatostatin analogues. Angewandte Chemie - International Edition, 47(14), 2595–2599. https://doi.org/10.1002/anie.200705797

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free