Synlett 1993; 1993(11): 821-826
DOI: 10.1055/s-1993-22619
account
© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. This journal, including all individual contributions and illustrations published therein, is legally protected by copyright for the duration of the copyright period. Any use, exploitation or commercialization outside the narrow limits set by copyright legislation, without the publisher's consent, is illegal and liable to criminal prosecution. This applies in particular to photostat reproduction, copying, cyclostyling, mimeographing or duplication of any kind, translating, preparation of microfilms, and electronic data processing and storage.

Peptide Secondary Structure Mimetics: Recent Advances and Future Challenges

Michael Kahn*
  • *Department of Pathobiology, University of Washington, Seattle, Washington 98195, and the Molecumetics Institute, 2023 120th Avenue N.E., Suite 400, Bellevue, Washington 98005, USA
Further Information

Publication History

Publication Date:
19 March 2002 (online)

An important goal of structural biochemistry is the reduction of complex molecules to small functional units that are amenable to high-resolution structural analysis and rapid modification. The dissection of multidomain proteins into small synthetic conformationally restricted components is an important step in the design of low molecular weight nonpeptides that mimic the activity of the native protein. Mimetics of critical functional domains might possess beneficial properties in comparison to the intact proteinaceous species with regard to specificity and therapeutic potential, and are valuable probes for the study of molecular recognition events. 1. Introduction 2. Peptidomimetic Discovery Strategies 3. The Secondary Structure Approach 4. First Generation Reverse Turn Mimetics 5. The Second Generation 6. Third Generation Mimetics 7. Conclusions