Solid-phase Synthesis of Peptidomimetics with Peptide Backbone Modifications

被引:16
作者
Abdildinova, Aizhan [1 ]
Kurth, Mark J. [2 ]
Gong, Young-Dae [1 ]
机构
[1] Dongguk Univ, Coll Sci, Dept Chem, Innovat Drug Lib Res Ctr, 26,3 Ga Pil Dong, Seoul 04620, South Korea
[2] Univ Calif Davis, Dept Chem, Davis, CA 95616 USA
基金
新加坡国家研究基金会;
关键词
foldamers; peptides; peptide backbone modifications; peptidomimetics; solid-phase synthesis; PROTEIN-PROTEIN INTERACTIONS; BETA-AMINO ACIDS; ALPHA/BETA-PEPTIDES; ANTIMICROBIAL ACTIVITY; GAMMA-AAPEPTIDES; ALIPHATIC OLIGOUREAS; SUBMONOMER SYNTHESIS; SECONDARY STRUCTURES; CIRCULAR-DICHROISM; HELICAL FOLDAMERS;
D O I
10.1002/ajoc.202100264
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Peptidomimetics are a class of compounds with promising pharmacological properties. Peptidomimetics reduce limitations of peptides including low bioavailability, poor stability, and poor cell-permeability. Peptide backbone modifications are a frequently used manipulation to reach desirable properties of the peptide molecules. The development of accessible synthetic methodologies plays an important role in peptidomimetic progress. Synthesis of peptidomimetics proceeds via solution and solid-phase synthesis strategies. Solid-phase organic synthesis serves as a powerful tool for the preparation of peptidomimetic molecules, thus, numerous strategies have been developed over the years. In this review, we discuss solid-phase synthetic approaches for peptide backbone modifications that were presented in the last two decades.
引用
收藏
页码:2300 / 2317
页数:18
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