Peptoid macrocycles: making the rounds with peptidomimetic oligomers

Barney Yoo, Sung Bin Y Shin, Mia Lace Huang, Kent Kirshenbaum

Research output: Contribution to journalArticle

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.

Original languageEnglish (US)
Pages (from-to)5527-5537
Number of pages11
JournalChemistry - A European Journal
Volume16
Issue number19
DOIs
StatePublished - May 17 2010

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Peptoids
Peptidomimetics
Oligomers
N-substituted Glycines
Conformations
Amino acids
Monomers

Keywords

  • Foldamers
  • Macrocycles
  • Peptidomimetics
  • Peptoids

ASJC Scopus subject areas

  • Chemistry(all)

Cite this

Peptoid macrocycles : making the rounds with peptidomimetic oligomers. / Yoo, Barney; Shin, Sung Bin Y; Huang, Mia Lace; Kirshenbaum, Kent.

In: Chemistry - A European Journal, Vol. 16, No. 19, 17.05.2010, p. 5527-5537.

Research output: Contribution to journalArticle

Yoo, Barney ; Shin, Sung Bin Y ; Huang, Mia Lace ; Kirshenbaum, Kent. / Peptoid macrocycles : making the rounds with peptidomimetic oligomers. In: Chemistry - A European Journal. 2010 ; Vol. 16, No. 19. pp. 5527-5537.
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