可药性
化学
肽
组合化学
甲基化
药物开发
生物利用度
氮原子
药品
计算生物学
肽合成
药理学
生物化学
有机化学
基因
医学
戒指(化学)
生物
作者
Xuefei Li,Ningchao Wang,Yuhang Liu,Weipiao Li,Xinyu Bai,Ping Liu,Chun‐Yang He
标识
DOI:10.1016/j.bioorg.2023.106892
摘要
Peptide-based drugs have garnered considerable attention in recent years owing to their increasingly crucial role in the treatment of diverse diseases. However, the limited pharmacokinetic properties of peptides have hindered their full potential. One prominent strategy for enhancing the druggability of peptides is N-methylation, which involves the addition of a methyl group to the nitrogen atom of the peptide backbone. This modification significantly improves the stability, bioavailability, receptor binding affinity and selectivity of peptide drug candidates. In this review, we provide a comprehensive overview of the advancements in synthetic methods for N-methylated peptide synthesis, as well as the associated limitations. Moreover, we explore the versatile effects of N-methylation on various aspects of peptide properties. Furthermore, we emphasize the efforts dedicated to N-methylated peptide pharmaceuticals that have successfully obtained marketing approval.
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