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pubmed-article:19189357pubmed:abstractTextA 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.lld:pubmed
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pubmed-article:19189357pubmed:dateRevised2010-11-18lld:pubmed
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pubmed-article:19189357pubmed:articleTitleDevelopment of tau aggregation inhibitors for Alzheimer's disease.lld:pubmed
pubmed-article:19189357pubmed:affiliationMax-Planck-Institute for Molecular Physiology, Dortmund, Germany. bruno.bulic@mpi-dortmund.mpg.delld:pubmed
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