Literature DB >> 29363202

Achieving Skeletal Diversity in Peptide Macrocycles through The Use of Heterocyclic Grafts.

Sherif J Kaldas1, Andrei K Yudin1.   

Abstract

Despite their therapeutic potential, peptide macrocycles often suffer from drawbacks such as low membrane permeability, proteolytic instability, and conformational lability. As a result, there have been significant efforts to "depeptidize" amino acid-rich macrocycles through the incorporation of heterocyclic grafts into their backbones. In this concept article, we summarize selected recent methodologies that can be used to introduce heterocycles into cyclic peptides.
© 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  bioactivity; heterocycles; macrocyclization; peptide chemistry; peptide macrocycles

Mesh:

Substances:

Year:  2018        PMID: 29363202     DOI: 10.1002/chem.201705418

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  1 in total

1.  Synthetic Lugdunin Analogues Reveal Essential Structural Motifs for Antimicrobial Action and Proton Translocation Capability.

Authors:  Nadine A Schilling; Anne Berscheid; Johannes Schumacher; Julian S Saur; Martin C Konnerth; Sebastian N Wirtz; José M Beltrán-Beleña; Alexander Zipperer; Bernhard Krismer; Andreas Peschel; Hubert Kalbacher; Heike Brötz-Oesterhelt; Claudia Steinem; Stephanie Grond
Journal:  Angew Chem Int Ed Engl       Date:  2019-05-27       Impact factor: 15.336

  1 in total

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