A Strategy To Prepare Peptide Heterodimers in the Solid Phase with an Acid-Labile Linker
Author:
Affiliation:
1. Beijing institute of Radiation Medicine, Beijing 100850, P.R. China
2. College of Engineering, Peking University, Beijing 100871, P.R. China
3. Beijing institute of Lifeomics, Beijing 102206, P.R. China
Funder
China Postdoctoral Science Foundation
National Natural Science Foundation of China
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.9b02638
Reference23 articles.
1. Relaxin, a pleiotropic vasodilator for the treatment of heart failure
2. Total Chemical Synthesis of a Heterodimeric Interchain Bis-Lactam-Linked Peptide: Application to an Analogue of Human Insulin-Like Peptide 3
3. Solid-Phase Synthesis of Disulfide Heterodimers of Peptides
4. Synthesis and characterization of the 47-residue heterodimeric antimicrobial peptide distinctin, featuring directed disulfide bridge formation
5. Δ‐Myrtoxin‐Mp1a is a Helical Heterodimer from the Venom of the Jack Jumper Ant that has Antimicrobial, Membrane‐Disrupting, and Nociceptive Activities
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