Protein-protein interactions as drug targets

被引:34
作者
Skwarczynska, Malgorzata [1 ]
Ottmann, Christian [2 ,3 ,4 ]
机构
[1] Lead Discovery Ctr GmbH, D-44227 Dortmund, Germany
[2] Tech Univ Eindhoven, Dept Biomed Engn, Biol Chem Lab, NL-5612 AZ Eindhoven, Netherlands
[3] Tech Univ Eindhoven, Inst Complex Mol Syst, Biol Chem Lab, NL-5612 AZ Eindhoven, Netherlands
[4] Univ Duisburg Essen, Dept Chem, D-45117 Essen, Germany
关键词
NITRIC-OXIDE SYNTHASE; SMALL-MOLECULE INHIBITORS; CD40-CD154 COSTIMULATORY INTERACTION; P-ARYLTHIO CINNAMIDES; PLANT; 14-3-3; PROTEINS; IN-VITRO; EDGETIC PERTURBATION; CELL-PROLIFERATION; LFA-1; INHIBITION; STRUCTURAL BASIS;
D O I
10.4155/fmc.15.138
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Modulation of protein-protein interactions (PPIs) is becoming increasingly important in drug discovery and chemical biology. While a few years ago this target class' was deemed to be largely undruggable an impressing number of publications and success stories now show that targeting PPIs with small, drug-like molecules indeed is a feasible approach. Here, we summarize the current state of small-molecule inhibition and stabilization of PPIs and review the active molecules from a structural and medicinal chemistry angle, especially focusing on the key examples of iNOS, LFA-1 and 14-3-3.
引用
收藏
页码:2195 / 2219
页数:25
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