Inhibition, ADME and structure based modification of IAA and IBA against acetylcholinesterase: an attempt towards new drug development for Alzheimer's disease

被引:11
作者
Dileep, K. V.
Remya, C.
Tintu, I.
Sadasivan, C. [1 ]
机构
[1] Kannur Univ, Dept Biotechnol & Microbiol, Palayad, India
来源
FRONTIERS IN LIFE SCIENCE | 2013年 / 7卷 / 3-4期
关键词
BChE; IAA; AChE; IBA; induced fit docking; TARGETED CANCER-THERAPY; HUMAN BUTYRYLCHOLINESTERASE; CHOLINERGIC HYPOTHESIS; CHOLINESTERASES; BINDING; DESIGN; ACID; DERIVATIVES;
D O I
10.1080/21553769.2013.876452
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Indole derived compounds have gained considerable attention in the pharmaceutical industry due to their pharmacological and structural properties. Indole-3-acetic acid (IAA) and indole 3-butyric acid (IBA) are two indole derivatives used in plant tissue culture experiments. They are plant growth regulators generally known as auxins. Since acetylcholinesterase (AChE) inhibitors prevent the hydrolysis of neurotransmitter acetylcholine, they may be suitable for the treatment of Alzheimer's disease. The IC50 and atomic level interaction of IAA and IBA against AChE were determined by enzyme inhibition and molecular docking studies. In order to improve central nervous system activity and blood brain permeability, in silico modification of the structure has been carried out. The modified compounds were screened by docking against AChE and butyrylcholinesterase (BChE). Based on the docking studies, four new derivatives have been identified for drug development against neurodegenerative disorders such as Alzheimer's disease.
引用
收藏
页码:164 / 173
页数:10
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