Novel Tacrine Analogs as Potential Cholinesterase Inhibitors in Alzheimer's Disease

被引:8
|
作者
El-Malah, Afaf [1 ]
Gedawy, Ehab M. [1 ]
Kassab, Asmaa E. [1 ]
Salam, Rania M. Abdel [2 ]
机构
[1] Cairo Univ, Dept Organ Pharmaceut Chem, Fac Pharm, Cairo 11562, Egypt
[2] Cairo Univ, Dept Pharmacol & Toxicol, Fac Pharm, Cairo 11562, Egypt
关键词
Acetylcholinesterase; Alzheimer's disease; Drug-likeness; Molecular-modeling; Tacrine; ACETYLCHOLINESTERASE INHIBITORS; BUTYRYLCHOLINESTERASE INHIBITORS; BIOLOGICAL EVALUATION; HIGHLY POTENT; DESIGN; SITE; HYPOTHESIS; BINDING; AGENTS;
D O I
10.1002/ardp.201300121
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Acetylcholinesterase inhibitors (AChEIs) are used for the treatment of Alzheimer's disease (AD). The increase in ACh levels ameliorates the symptoms of the disease. Tacrine is the first clinically approved drug as AChEI used in the treatment of AD. In this paper, we synthesized new tacrine analogs to act on catalytic and peripheral sites of AChE. Their inhibitory activity was evaluated. All novel compounds except 7a showed promising results toward AChE. Two compounds, 10b and 11b, are more potent than tacrine. Furthermore, molecular-modeling studies were performed for these two compounds to rationalize the obtained pharmacological activity. Moreover, various drug-likeness properties of the new compounds were predicted.
引用
收藏
页码:96 / 103
页数:8
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