Original ArticleIndian Journal of Pharmaceutical Education and ResearchVol. 52 | Issue 4 | 2018 | pp. 644–654Open access
Design, Synthesis and Evaluation of 4-Aminopyridine Analogues as Cholinesterase Inhibitors for Management of Alzheimer’s Diseases
- 1,
- 2,
- 3*
- 1 Faculty of Pharmacy, Pacific Academy of Higher Education and Research University, Udaipur, Rajasthan, INDIA.
- 2 Department of Pharmaceutical Sciences, Mohanlal Sukhadia University, Udaipur, Rajasthan, INDIA.
- 3 Faculty of Pharmacy, Pacific Academy of Higher Education and Research University, Udaipur, Rajasthan, INDIA.
Published in Indian Journal of Pharmaceutical Education and Research
Correspondence: Mrunal Krishnarao Shirsat
Faculty of Pharmacy, Pacific Academy of Higher Education and Research University, Udaipur, Rajasthan, INDIA.
Email: mrunalvir@gmail.com
Copyright: © 2018 Manuscript Technomedia. This is an open access article.
- Published:
- Jun 20, 2018
- Received:
- Sep 26, 2017
- Accepted:
- Apr 18, 2018
How to cite
Singh, S. K., Sinha, S. K., & Shirsat, M. K. (2018). Design, Synthesis and Evaluation of 4-Aminopyridine Analogues as Cholinesterase Inhibitors for Management of Alzheimer’s Diseases. Indian Journal of Pharmaceutical Education and Research, 52(4), 644–654. https://doi.org/10.5530/ijper.52.4.75
Abstract
Introduction: Alzheimer’s disease (AD) is a slowly progressive devasting neurodegenerative disorder of central nervous system manifested by deterioration of memory, cognitive functions, behaviour change and impairment in performing activities of daily life. Neurochemical studies of patients suffering from AD demonstrate selective loss of cholinergic neurons, low concentration of acetylcholine (Ach) in the selective areas of brain such as cortex and hippocampus. Objective: A series of new semicarbazones of 4-aminopyridine has been designed, synthesized and evaluated for cognition enhancing activities through the inhibition of acetylcholinesterase (AChE) and by passive avoidance model. Material and methods: In the present study, ten new 4-Aminopyridine analogues were synthesized and characterized by analytic methods such as UV, IR, NMR, elemental analysis and for their inhibitory role on Acetylcholinesterase activity by applying the molecular docking studies and performed enzyme kinetics study by Ellman’s spectrophotometric method. The synthesized analogues were then evaluated for antiamnesic and cognition enhancing activities by passive avoidance test. Results: The results illustrated a significant cognition enhancing effect on passive avoidance test with a significant reversal of scopolamine-induced amnesia, which is comparable with standard drug rivastigmine. The in-vitro study of synthesized analogues showed maximum activity of compound-3 and compound-9 compared to standard drug rivastigmine, whereas its enzyme kinetic study revealed a non-competitive inhibition of acetylcholinesterase (AChE) is held responsible to a possible interaction of analogue with the peripheral anionic site (PAS) of AChE and was also confirmed by molecular docking studies. Conclusion: On the basis of present study, we are concluding that hydroxyl substituted Compound 3 and 9 identified as most potent drug which can leads to the discovery and development of new Cognition enhancers in near future.
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Article metadata
| Title | Design, Synthesis and Evaluation of 4-Aminopyridine Analogues as Cholinesterase Inhibitors for Management of Alzheimer’s Diseases |
|---|---|
| Authors | Shashi Kant Singh; Saurabh Kumar Sinha; Mrunal Krishnarao Shirsat |
| Affiliations | Faculty of Pharmacy, Pacific Academy of Higher Education and Research University, Udaipur, Rajasthan, INDIA.; Department of Pharmaceutical Sciences, Mohanlal Sukhadia University, Udaipur, Rajasthan, INDIA.; Faculty of Pharmacy, Pacific Academy of Higher Education and Research University, Udaipur, Rajasthan, INDIA. |
| Corresponding author | mrunalvir@gmail.com |
| Journal | Indian Journal of Pharmaceutical Education and Research |
| Volume / Issue | Vol. 52, Issue 4 (2018) |
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