Novel Antibiotics: Macrocyclic Peptides Designed to Trap Holliday Junctions
Author:
Affiliation:
1. Department of Chemistry, Molecular Biology Institute, and Center for Applied and Experimental Genomics, 5500 Campanile Drive, 208 CSL, San Diego State University, San Diego, California 92182-1030
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol020204f
Reference20 articles.
1. Hirschmann, R.; Smith, A. B.; Sprengeler, P. A.New Perspectives in DrugDesign; Dean, M., Newton, C. G., Eds.; Academic Press, Inc. New York, 1995; p 1. (b) West, M. L.; Fairlie, P. D.Trends Pharm. Sci.1995,16, 67.
2. (b) Albericio, F.; Carpino, L. A. InMethods in Enzymology; Fields, G. B., Ed.; Academic Press: New York, 1997; pp 104−126.
3. Chemical Synthesis of Natural Product Peptides: Coupling Methods for the Incorporation of Noncoded Amino Acids into Peptides
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