Recent progress on total synthesis of cyclic peptides

被引:4
|
作者
Liu, Haiping [1 ]
Bai, Leiyang [1 ]
Jiang, Xuefeng [1 ,2 ,3 ]
机构
[1] East China Normal Univ, Hainan Inst, Sch Chem & Mol Engn, State Key Lab Petr Mol & Proc Engn,Shanghai Key La, 3663 North Zhongshan Rd, Shanghai 200062, Peoples R China
[2] Henan Normal Univ, Sch Chem & Chem Engn, Xinxiang 453007, Henan, Peoples R China
[3] Chinese Acad Sci, State Key Lab Organometall Chem, Shanghai Inst Organ Chem, 345 Lingling Rd, Shanghai 200032, Peoples R China
基金
中国博士后科学基金;
关键词
Cyclic peptides; Bicyclic peptides; Tricyclic peptides; Total synthesis; Peptide therapeutics; HIMASTATIN; INHIBITOR; CHLORIDES;
D O I
10.1016/j.tetlet.2024.155314
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
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 drug discovery.
引用
收藏
页数:19
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