Peptoid macrocycles: Making the rounds with peptidomimetic oligomers Journal Article


Authors: Yoo, B.; Shin, S. B. Y.; Huang, M. L.; Kirshenbaum, K.
Article Title: Peptoid macrocycles: Making the rounds with peptidomimetic oligomers
Abstract: Macrocyclic constraints are often employed to rigidify the conformation of flexible oligomeric systems. This approach has recently been used to organize the structure of peptoid oligomers, which are peptidomimetics composed of chemically diverse N-substituted glycine monomer units. In this review, we describe advances in the synthesis and characterization of cyclic peptoids. We evaluate how the installation of covalent constraints between the oligomer termini or side chains has been effective in defining peptoid conformations. We also discuss the potential applications for this promising family of macrocyclic peptidomimetics. © 2010 Wiley-VCH Verlag GmbH& Co. KGaA.
Keywords: synthesis (chemical); side chains; macrocycles; conformations; foldamers; peptidomimetics; peptoids; macrocyclic peptidomimetics; macrocyclics; monomer units; potential applications; synthesis and characterization; amphiphiles; oligomers
Journal Title: Chemistry - A European Journal
Volume: 16
Issue: 19
ISSN: 0947-6539
Publisher: Wiley V C H Verlag Gmbh  
Date Published: 2010-05-17
Start Page: 5527
Language: English
DOI: 10.1002/chem.200903549
PROVIDER: scopus
PUBMED: 20414912
DOI/URL:
Notes: --- - "Export Date: 20 April 2011" - "CODEN: CEUJE" - "Source: Scopus"
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  1. Barney Yoo
    13 Yoo