Neuroactive Multifunctional Tacrine Congeners with Cholinesterase, Anti-Amyloid Aggregation and Neuroprotective PropertiesReportar como inadecuado




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1

Department of Biochemistry, Institute of Chemistry, P. J. Šafárik University, Moyzesova 11, Košice, Slovakia

2

Department of Organic Chemistry, Institute of Chemistry, P. J. Šafárik University, Moyzesova 11, Košice, Slovakia

3

Department of Biophysics, Institute of Experimental Physics, Slovak Academy of Sciences, Watsonova 47, Košice, Slovakia

4

Department of Biochemistry and Microbiology, Faculty of Chemical and Food Technology, Slovak University of Technology, Radlinského 9, Bratislava, Slovakia





*

Author to whom correspondence should be addressed.



Abstract The review summarizes research into the highly relevant topics of cholinesterase and amyloid aggregation inhibitors connected to tacrine congeners, both of which are associated with neurogenerative diseases. Various opinions will be discussed regarding the dual binding site inhibitors which are characterized by increased inhibitor potency against acetylcholin-butyrylcholine esterase and amyloid formation. It is suggested that these compounds can both raise levels of acetylcholine by binding to the active site, and also prevent amyloid aggregation. In connection with this problem, the mono-dual binding of the multifunctional derivatives of tacrine, their mode of action and their neuroprotective activities are reported. The influence of low molecular compounds on protein amyloid aggregation, which might be considered as a potential therapeutic strategy in the treatment of Alzheimer’s disease is also reported. Finally, attention is paid to some physico-chemical factors, such as desolvation energies describing the transfer of the substrate solvated by water, the metal-chelating properties of biometals reacting with amyloid precursor protein, amyloid beta peptide and tau protein. View Full-Text

Keywords: tacrine; acetylcholinesterase inhibitor; amyloid aggregation; Alzheimer’s disease tacrine; acetylcholinesterase inhibitor; amyloid aggregation; Alzheimer’s disease





Autor: Maria Kozurkova 1,* , Slavka Hamulakova 2, Zuzana Gazova 3, Helena Paulikova 4 and Pavol Kristian 2

Fuente: http://mdpi.com/



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