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
相关论文
共 96 条
  • [91] Selective inhibition of Alzheimer disease-like tau aggregation by phenothiazines
    Wischik, CM
    Edwards, PC
    Lai, RYK
    Roth, M
    Harrington, CR
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (20) : 11213 - 11218
  • [92] WISCHIK CM, 2007, Patent No. 2007110630
  • [93] WISCHIK CM, 2008, INT C ALZH DIS CHIC
  • [94] Curcumin inhibits formation of amyloid β oligomers and fibrils, binds plaques, and reduces amyloid in vivo
    Yang, FS
    Lim, GP
    Begum, AN
    Ubeda, OJ
    Simmons, MR
    Ambegaokar, SS
    Chen, PP
    Kayed, R
    Glabe, CG
    Frautschy, SA
    Cole, GM
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (07) : 5892 - 5901
  • [95] Delineation of positron emission tomography imaging agent binding sites on β-amyloid peptide fibrils
    Ye, L
    Morgenstern, JL
    Gee, AD
    Hong, GZ
    Brown, J
    Lockhart, A
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (25) : 23599 - 23604
  • [96] A simple statistical parameter for use in evaluation and validation of high throughput screening assays
    Zhang, JH
    Chung, TDY
    Oldenburg, KR
    [J]. JOURNAL OF BIOMOLECULAR SCREENING, 1999, 4 (02) : 67 - 73