摘要
Cyclic peptides are composed of canonical and non-canonical amino acids in a rigid conformation, which endow them high binding affinity and specificity, proteolytic stability, and enhanced membrane permeation compared to linear analogs, thereby making them as promising therapeutics of the future. To date, more than 40 cyclic peptides from nature or derivatives are used as therapeutics, with an average of around one cyclic peptide drug approved per year. This review aims to highlight the past 5 years’ advances in total synthesis of cyclic peptides including monocyclic peptides, bicyclic peptides, and tricyclic peptides, laying a solidly synthetic foundation for drug discovery.
| 源语言 | 英语 |
|---|---|
| 文章编号 | 155314 |
| 期刊 | Tetrahedron Letters |
| 卷 | 151 |
| DOI | |
| 出版状态 | 已出版 - 13 11月 2024 |
指纹
探究 'Recent progress on total synthesis of cyclic peptides' 的科研主题。它们共同构成独一无二的指纹。引用此
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