Design, synthesis, and applications of ring-functionalized histidines in peptide-based medicinal chemistry and drug discovery

被引:6
作者
Sharma, Komal [1 ]
Sharma, Krishna K. [1 ]
Mahindra, Amit [1 ]
Sehra, Naina [1 ]
Bagra, Nitin [1 ]
Aaghaz, Shams [1 ]
Parmar, Rajesh [1 ]
Rathod, Gajanan K. [1 ]
Jain, Rahul [1 ,2 ]
机构
[1] Natl Inst Pharmaceut Educ & Res, Dept Med Chem, Nagar, Punjab, India
[2] Natl Inst Pharmaceut Educ & Res, Dept Med Chem, Sect 67, SAS Nagar 160062, Punjab, India
关键词
amino acid functionalization; antimicrobial peptides; CNS active peptides; functionalized histidines; synthetic peptides; THYROTROPIN-RELEASING-HORMONE; EXHIBITS POTENT INHIBITION; IN-VIVO MODELS; AMINO-ACIDS; REGIOSPECIFIC SYNTHESIS; DIAZONIUM SALTS; BIOSYNTHETIC INCORPORATION; ANTIMICROBIAL ACTIVITIES; BROMOBENZENE 3,4-OXIDE; BIOLOGICAL EVALUATION;
D O I
10.1002/med.21936
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Modified and synthetic alpha-amino acids are known to show diverse applications. Histidine, which possesses numerous applications when subjected to synthetic modifications, is one such amino acid. The utility of modified histidines varies widely from remarkable biological activities to catalysis, and from nanotechnology to polymer chemistry. This renders histidine residue an important place in scientific research. Histidine is a well-studied scaffold and constitutes the active site of various enzymes catalyzing important reactions in the biological systems. A rational modification in histidine structure with a distinctly developed protocol extensively changes its physical and chemical properties. The utilization of modified histidines in search of potent, target selective and proteostable scaffolds is vital in the development of bioactive peptides with enhanced drug-likeliness. This review is a compilation and analysis of reported side-chain ring modifications at histidine followed by applications of ring-modified histidines in the synthesis of various categories of bioactive peptides and peptidomimetics.
引用
收藏
页码:775 / 828
页数:54
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