Introducing sequential aza-amino acids units induces repeated β-turns and helical conformations in peptides

Org. Biomol. Chem., 2020, Accepted Manuscript DOI: 10.1039/C9OB02654A, CommunicationNicolo Tonali, Isabelle Correia, Jacopo Lesma, Guillaume Bernadat, Sandrine Ongeri, Olivier LEQUIN A major current issue in medicinal chemistry is the design of small peptide analogues resistant to proteolysis and able to adopt preferential conformations, while preserving the selectivity and efficiency of... The content of this RSS Feed (c) The Royal Society of Chemistry

Source: RSC - Organic and Biomolecular Chemistry - February 17, 2020 Category: Molecular Biology Authors: Nicolo Tonali Source Type: research