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Backbone N-methylation of peptides: Advances in synthesis and applications in pharmaceutical drug development
被引:14
|作者:
Li, Xuefei
[1
,2
]
Wang, Ningchao
[2
]
Liu, Yuhang
[2
]
Li, Weipiao
[1
]
Bai, Xinyu
[1
]
Liu, Ping
[1
]
He, Chun -Yang
[1
]
机构:
[1] Zunyi Med Univ, Minist Educ, Key Lab Biocatalysis & Chiral Drug Synth Guizhou P, Key Lab Basic Pharmacol, 6 West Xuefu Rd, Zunyi 563000, Guizhou, Peoples R China
[2] United Imaging Healthcare Grp Co Ltd, Cent Res Inst, Shanghai, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Peptide synthesis;
Pharmacological impact;
Pharmaceutical drugs;
N-methylation;
IN-VITRO SELECTION;
SOLID-PHASE SYNTHESIS;
AMINO-ACIDS;
RIBOSOMAL SYNTHESIS;
STRUCTURAL BASIS;
METAL-ION;
TOXICITY;
BONDS;
CYCLOSPORINE;
INHIBITION;
D O I:
10.1016/j.bioorg.2023.106892
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
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 Nmethylated peptide pharmaceuticals that have successfully obtained marketing approval.
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页数:19
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