Peptide Macrocyclization Inspired by Non-Ribosomal Imine Natural Products-Reference-Cited by-同舟云学术

Peptide Macrocyclization Inspired by Non-Ribosomal Imine Natural Products

Published:2017-03-31 Issue:14 Volume:139 Page:5233-5241
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Malins Lara R.¹,deGruyter Justine N.¹^ORCID,Robbins Kevin J.²,Scola Paul M.²,Eastgate Martin D.³,Ghadiri M. Reza¹,Baran Phil S.¹^ORCID

Affiliation:

1. Department of Chemistry, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, United States

2. Department of Discovery Chemistry, Bristol-Myers Squibb Research and Development, 5 Research Parkway, Wallingford, Connecticut 06492, United States

3. Chemical Development, Bristol-Myers Squibb, One Squibb Drive, New Brunswick, New Jersey 08903, United States

Funder

National Institute of General Medical Sciences

National Science Foundation

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

http://pubs.acs.org/doi/pdf/10.1021/jacs.7b01624

Reference58 articles.

1. The Future of Peptide-based Drugs

2. Peptide-based inhibitors of protein–protein interactions

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4. Small molecules, big targets: drug discovery faces the protein–protein interaction challenge

5. Strategic Approaches to Optimizing Peptide ADME Properties

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