Progress and Developments in Tau Aggregation Inhibitors for Alzheimer Disease

被引:94
作者
Bulic, Bruno [1 ]
Pickhardt, Marcus [2 ]
Mandelkow, Eckhard [2 ,3 ,4 ]
机构
[1] Humboldt Univ, Lab Organ Synth Funct Syst, D-12489 Berlin, Germany
[2] DZNE German Ctr Neurodegenerat Dis, D-53175 Bonn, Germany
[3] CAESAR Res Ctr, D-53175 Bonn, Germany
[4] DESY, Max Planck Inst Neurol Res, Hamburg Outstn, D-22607 Hamburg, Germany
基金
英国惠康基金;
关键词
PAIRED HELICAL FILAMENTS; SMALL-MOLECULE INHIBITORS; PROTEIN-PROTEIN INTERACTIONS; AMYLOID-BETA-PEPTIDE; METHYLENE-BLUE; IN-VITRO; A-BETA; RHODANINE DERIVATIVES; PHOSPHORYLATED TAU; THIOFLAVIN-T;
D O I
10.1021/jm3017317
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Pharmacological approaches directed toward Alzheimer disease are diversifying in parallel with a growing number of promising targets. Investigations on the microtubule-associated protein tau yielded innovative targets backed by recent findings about the central role of tau in numerous neurodegenerative diseases. In this review, we summarize the recent evolution in the development of nonpeptidic small molecules tau aggregation inhibitors (TAGIs) and their advancement toward clinical trials. The compounds are classified according to their chemical structures, providing correlative insights into their pharmacology. Overall, shared structure-activity traits are emerging, as well as specific binding modes related to their ability to engage in hydrogen bonding. Medicinal chemistry efforts on TAGIs together with encouraging in vivo data argue for successful translation to the clinic.
引用
收藏
页码:4135 / 4155
页数:21
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