New indole derivatives as multitarget anti-Alzheimer's agents: synthesis, biological evaluation and molecular dynamics

被引:6
|
作者
Azmy, Eman M. [1 ]
Nassar, Ibrahim F. [2 ]
Hagras, Mohamed [3 ]
Fawzy, Iten M. [4 ]
Hegazy, Maghawry [5 ]
Mokhtar, Mahmoud Mohamed [5 ]
Yehia, Amr Mohamed [5 ]
Ismail, Nasser S. M. [4 ]
Lashin, Walaa H. [1 ]
机构
[1] Ain Shams Univ, Fac Women, Dept Chem, Cairo 11457, Egypt
[2] Ain Shams Univ, Fac Specif Educ, 365 Ramsis St, Cairo, Egypt
[3] Al Azhar Univ, Coll Pharm Boys, Dept Pharmaceut Organ Chem, Cairo 11884, Egypt
[4] Future Univ Egypt, Fac Pharm, Dept Pharmaceut Chem, Cairo 11835, Egypt
[5] Al Azhar Univ, Fac Pharm Boys, Biochem & Mol Biol Dept, Cairo, Egypt
关键词
AChE; Alzheimer's disease; BChE; indole derivatives; molecular dynamic simulations; TARGET-DIRECTED LIGANDS; ACETYLCHOLINESTERASE INHIBITORS; DISEASE; DESIGN; AGGREGATION; DISCOVERY; DONEPEZIL; HYBRIDS; BETA; TAU;
D O I
10.4155/fmc-2022-0228
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Background: Alzheimer's disease is a neurological disorder that causes brain cells to shrink and die. Aim: Thirteen novel 'oxathiolanyl', 'pyrazolyl' and 'pyrimidinyl' indole derivatives were designed and synthesized as anti-Alzheimer's disease treatment. Method: In vitro enzyme assay was performed against both AChE and BChE enzymes. In addition, antioxidant assay and cytotoxicity on a normal cell line were determined. Molecular docking and dynamic simulations were conducted to confirm the binding mode in both esterases' active sites. In silico absorption, distribution, metabolism, excretion and toxicity studies were also carried out. Results & conclusion: Compounds 5, 7 and 11 exhibited superior inhibitory activity against acetylcholinesterase and butyrylcholinesterase, with IC50 values of 0.042 and 3.003 mu M, 2.54 and 0.207 mu M and 0.052 and 2.529 mu M, respectively, compared with donepezil.
引用
收藏
页码:473 / 495
页数:23
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