Relaxin family peptides: structure-activity relationship studies

被引:70
|
作者
Patil, Nitin A. [1 ,2 ]
Rosengren, K. Johan [3 ]
Separovic, Frances [2 ]
Wade, John D. [1 ,2 ]
Bathgate, Ross A. D. [1 ,3 ]
Hossain, Mohammed Akhter [1 ,2 ]
机构
[1] Univ Melbourne, Florey Inst Neurosci & Mental Hlth, Parkville, Vic 3010, Australia
[2] Univ Melbourne, Sch Chem, Parkville, Vic, Australia
[3] Univ Melbourne, Dept Biochem & Mol Biol, Parkville, Vic, Australia
基金
澳大利亚国家健康与医学研究理事会; 英国医学研究理事会; 澳大利亚研究理事会;
关键词
D O I
10.1111/bph.13684
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The human relaxin peptide family consists of seven cystine-rich peptides, four of which are known to signal through relaxin family peptide receptors, RXFP1-4. As these peptides play a vital role physiologically and in various diseases, they are of considerable importance for drug discovery and development. Detailed structure-activity relationship (SAR) studies towards understanding the role of important residues in each of these peptides have been reported over the years and utilized for the design of antagonists and minimized agonist variants. This review summarizes the current knowledge of the SAR of human relaxin 2 (H2 relaxin), human relaxin 3 (H3 relaxin), human insulin-like peptide 3 (INSL3) and human insulin-like peptide 5 (INSL5).
引用
收藏
页码:950 / 961
页数:12
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