Synthesis and Evaluation of Anti-acetylcholinesterase Activity of 2-(2-(4-(2-Oxo-2-phenylethyl)piperazin-1-yl) ethyl)Isoindoline-1,3-dione Derivatives with Potential Anti-Alzheimer Effects

被引:0
|
作者
Aliabadi, Alireza [1 ,2 ]
Foroumadi, Alireza [3 ,4 ]
Mohammadi-Farani, Ahmad [1 ,5 ]
Mahvar, Mahdi Garmsiri [2 ,6 ]
机构
[1] Kermanshah Univ Med Sci, Novel Drug Delivery Res Ctr, Kermanshah, Iran
[2] Kermanshah Univ Med Sci, Fac Pharm, Dept Med Chem, Kermanshah, Iran
[3] Univ Tehran Med Sci, Fac Pharm, Dept Med Chem, Tehran, Iran
[4] Univ Tehran Med Sci, Pharmaceut Sci Res Ctr, Tehran, Iran
[5] Kermanshah Univ Med Sci, Fac Pharm, Dept Pharmacol Toxicol & Med Serv, Kermanshah, Iran
[6] Kermanshah Univ Med Sci, Students Res Comm, Kermanshah, Iran
关键词
Acetylcholinesterase; Alzheimer; Phthalimide; Synthesis; ACETYLCHOLINESTERASE INHIBITORS; ANTICHOLINESTERASE ACTIVITY; 3D STRUCTURE; DESIGN; CHOLINESTERASE; DISEASE;
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Objective(s): Alzheimer's disease (AD) is a neurodegenerative disorder in elderly patients. Decrease in cholinergic neurotransmission is the main known cause in the pathophysiology of the disease. Improvement and potentiation of the cholinergic system could be beneficial for treatment of the AD. Acetylcholinesterase inhibitors such as donepezil can enhance the duration of action of acetylcholine (Ach) and therefore, through this mechanism improve the symptoms of AD. Materials and Methods: In the current study, based on the potential inhibitory activity of phthalimide derivatives towards acetylcholinesterase enzyme, a new series of phthalimide-based compounds were synthesized (4a-4e) and anti-acetylcholinesterase effect was assessed using Ellman's test. Compound 4b with 4-Fluorophenyl moiety was the most potent derivative in this series (IC50 = 16.42 +/- 1.07 mu M). It was shown that, none of the synthesized compounds showed superior inhibitory potency compared to donepezil (0.41 +/- 0.09 mu M) as a reference drug. Conclusion: The new synthesized phthalimide based analogs could function as potential acetylcholinesterase inhibitors. Further studies are necessary for development of potent analogs.
引用
收藏
页码:1049 / 1054
页数:6
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