Applying Promiscuous RiPP Enzymes to Peptide Backbone N-Methylation Chemistry
Author:
Affiliation:
1. Department of Medicinal Chemistry, University of Utah, Salt Lake City, Utah 84112, United States
Funder
National Institute of General Medical Sciences
Publisher
American Chemical Society (ACS)
Subject
Molecular Medicine,General Medicine,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acschembio.2c00293
Reference49 articles.
1. Peptide Therapeutics 2.0
2. Peptide therapeutics: current status and future directions
3. Macrocyclic Peptides as Drug Candidates: Recent Progress and Remaining Challenges
4. Improving Oral Bioavailability of Peptides by Multiple N-Methylation: Somatostatin Analogues
5. Multiple N-Methylation of MT-II Backbone Amide Bonds Leads to Melanocortin Receptor Subtype hMC1R Selectivity: Pharmacological and Conformational Studies
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