The use of phosphate bioisosteres in medicinal chemistry and chemical biology

被引:144
作者
Elliott, Thomas S. [2 ,3 ]
Slowey, Aine [1 ]
Ye, Yulin [1 ]
Conway, Stuart J. [1 ]
机构
[1] Univ Oxford, Chem Res Lab, Dept Chem, Oxford OX1 3TA, England
[2] Univ St Andrews, Sch Chem, St Andrews KY16 9ST, Fife, Scotland
[3] Univ St Andrews, Ctr Biomol Sci, St Andrews KY16 9ST, Fife, Scotland
关键词
STRUCTURE-BASED DESIGN; 2-ARYLTHIAZOLIDINE-4-CARBOXYLIC ACID-AMIDES; X-RAY-STRUCTURE; STRUCTURAL BASIS; SH2; DOMAIN; MYOINOSITOL 1,4,5-TRISPHOSPHATE; RESISTANT ANALOGS; CYTOTOXIC AGENTS; LYSOPHOSPHATIDIC ACID; 5-PHOSPHONATE ANALOGS;
D O I
10.1039/c2md20079a
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
Phosphate and pyrophosphate groups play a central role in cellular signalling and consequently are of great interest to both medicinal chemists and chemical biologists. However, the design of molecules that can interfere with phosphate-based processes is recognised as a significant challenge, especially when the resulting compounds must show good cellular penetration and stability. Herein, we have reviewed the full range of phosphate bioisosteres currently reported and provided the context of their deployment. We aim to provide a useful reference for medicinal chemists and chemical biologists who are engaged in the design of molecules that target phosphate-binding proteins.
引用
收藏
页码:735 / 751
页数:17
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