4.8 Article

Pyrrolinone-Pyrrolidine Oligomers as Universal Peptidomimetics

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 133, Issue 32, Pages 12350-12353

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ja2033734

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Funding

  1. National Institutes of Health [GM087981]
  2. Robert A. Welch Foundation [A-1121]

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Peptidomimetics 1-3 were prepared from amino acid-derived tetramic acids 7 as the key starting materials. Calculations show that preferred conformations of 1 can align their side-chain vectors with amino acids in common secondary structures more effectively than conformations of 3. A good fit was found for a preferred conformation of 2 (an extended derivative of 1) with a sheet/beta-turn/sheet motif.

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