Synthesis and DPPH scavenging assay of reserpine analogues, computational studies and in silico docking studies in AChE and BChE responsible for Alzheimer's disease

Authors

  • Muhammad Yar COMSATS Institute of Information Technology; Interdisciplinary Research Centre in Biomedical Materials; COMSATS Institute of Information Technology
  • Muhammad Arshad COMSATS Institute of Information Technology; Department of Chemistry; COMSATS Institute of Information Technology
  • Ariba Farooq COMSATS Institute of Information Technology; Interdisciplinary Research Centre in Biomedical Materials; COMSATS Institute of Information Technology
  • Mazhar Amjad Gilani COMSATS Institute of Information Technology; Department of Chemical Engineering; COMSATS Institute of Information Technology
  • Khurshid Ayub King Faisal University; College of Science; Department of Chemistry; King Faisal University
  • Asma Ejaz University of Karachi; Hussain Ibrahim Jamal Research Institute of Chemistry; International Center for Chemical and Biological Sciences; University of Karachi
  • Anupriya Kumar Nagoya University; Institute of Transformative Bio-Molecules; Nagoya University
  • Ichiya Ninomiya University of Karachi; Hussain Ibrahim Jamal Research Institute of Chemistry; International Center for Chemical and Biological Sciences; University of Karachi

DOI:

https://doi.org/10.1590/S1984-82502015000100006

Abstract

Alzheimer's disease (AD) is a fast growing neurodegenerative disorder of the central nervous system and anti-oxidants can be used to help suppress the oxidative stress caused by the free radicals that are responsible for AD. A series of selected synthetic indole derivatives were biologically evaluated to identify potent new antioxidants. Most of the evaluated compounds showed significant to modest antioxidant properties (IC50 value 399.07 140.0±50 µM). Density Functional Theory (DFT) studies were carried out on the compounds and their corresponding free radicals. Differences in the energy of the parent compounds and their corresponding free radicals provided a good justification for the trend found in their IC50 values. In silico, docking of compounds into the proteins acetylcholinesterase (AChE) and butyrylcholinesterase (BChE), which are well known for contributing in AD disease, was also performed to predict anti-AD potential.

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Published

2015-03-01

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Articles

How to Cite

Synthesis and DPPH scavenging assay of reserpine analogues, computational studies and in silico docking studies in AChE and BChE responsible for Alzheimer’s disease . (2015). Brazilian Journal of Pharmaceutical Sciences, 51(1), 53-61. https://doi.org/10.1590/S1984-82502015000100006