Development of Tau Aggregation Inhibitors for Alzheimer's Disease

被引:227
作者
Bulic, Bruno [1 ,2 ,3 ]
Pickhardt, Marcus [4 ]
Schmidt, Boris [5 ]
Mandelkow, Eva-Maria [4 ]
Waldmann, Herbert [1 ,2 ,3 ]
Mandelkow, Eckhard [4 ]
机构
[1] Max Planck Inst Mol Physiol, D-44139 Dortmund, Germany
[2] Ctr Appl Chem Genom, Dortmund, Germany
[3] Tech Univ Dortmund, Dortmund, Germany
[4] DESY, Max Planck Unit Struct Mol Biol, D-22607 Hamburg, Germany
[5] Tech Univ Darmstadt, Clemens Schopf Inst Organ Chem & Biochem, D-64287 Darmstadt, Germany
关键词
aggregation inhibitors; Alzheimer's disease; amyloids; neurodegeneration; Tau protein; PAIRED HELICAL FILAMENTS; SMALL-MOLECULE INHIBITORS; AMYLOID-BETA; CONGO RED; CELL MODELS; IN-VITRO; AROMATIC INTERACTIONS; FIBRIL FORMATION; TRANSGENIC MICE; THIOFLAVIN-T;
D O I
10.1002/anie.200802621
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A variety of human diseases are suspected to be directly linked to protein misfolding. Highly organized protein aggregates, called amyloid fibrils, and aggregation intermediates are observed; these are considered to be mediators of cellular toxicity and thus attract a great deal of attention from investigators. Neurodegenerative pathologies such as Alzheimer's disease account for a major part of these protein misfolding diseases. The last decade has witnessed a renaissance of interest in inhibitors of tau aggregation as potential disease-modifying drugs for Alzheimer's disease and other tauopathies". The recent report of a phase II clinical trial with the tau aggregation inhibitor MTC could hold promise for the validation of the concept. This Review summarizes the available data concerning small-molecule inhibitors of tau aggregation from a medicinal chemistry point of view. © 2009 Wiley-VCH Verlag GmbH & Co. KGaA."
引用
收藏
页码:1741 / 1752
页数:12
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