Recent Molecular Targets and Their Ligands for the Treatment of Alzheimer Disease

被引:1
作者
Bayraktar, Guelsah [1 ]
Alptuezuen, Vildan [1 ]
机构
[1] Ege Univ, Fac Pharm, Dept Pharmaceut Chem, TR-35040 Izmir, Turkiye
关键词
Alzheimer's disease; cannabinoid receptors; matrix metalloproteinases; histone deacetylases; glycogen synthase kinase-3 beta; mitogen-activated protein kinases; c-Jun N-terminal kinases; MATRIX METALLOPROTEINASES; BIOLOGICAL EVALUATION; THERAPEUTIC TARGET; CB2; RECEPTOR; GSK-3-BETA INHIBITORS; IN-VITRO; POTENT; DISCOVERY; AGENTS; DERIVATIVES;
D O I
10.2174/0115680266318722240809050235
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Alzheimer's disease is a multifaceted neurodegenerative disease. Cholinergic dysfunction, amyloid beta toxicity, tauopathies, oxidative stress, neuroinflammation are among the main pathologies of the disease. Ligands targeting more than one pathology, multi-target directed ligands, attract attention in the recent years to tackle Alzheimer's disease. In this review, we aimed to cover different biochemical pathways, that are revealed in recent years for the pathology of the disease, as druggable targets such as cannabinoid receptors, matrix metalloproteinases, histone deacetylase and various kinases including, glycogen synthase kinase-3, mitogen-activated protein kinase and c-Jun N-terminal kinase, and their ligands for the treatment of Alzheimer's disease in the hope of providing more realistic insights into the field.
引用
收藏
页码:2447 / 2464
页数:18
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